共 50 条
- [41] Further clinical delineation in trisomy 1q32 syndromeANNALES DE GENETIQUE, 2001, 44 (04): : 175 - 177Nuño-Arana, I论文数: 0 引用数: 0 h-index: 0机构: Univ Guadalajara, Div Genet, Ctr Invest Biomed Occidente,CMNO,IMSS, Ctr Univ Ciencias Salud, Guadalajara 44340, Jalisco, Mexico Univ Guadalajara, Div Genet, Ctr Invest Biomed Occidente,CMNO,IMSS, Ctr Univ Ciencias Salud, Guadalajara 44340, Jalisco, MexicoGonzález-García, JR论文数: 0 引用数: 0 h-index: 0机构: Univ Guadalajara, Div Genet, Ctr Invest Biomed Occidente,CMNO,IMSS, Ctr Univ Ciencias Salud, Guadalajara 44340, Jalisco, Mexico Univ Guadalajara, Div Genet, Ctr Invest Biomed Occidente,CMNO,IMSS, Ctr Univ Ciencias Salud, Guadalajara 44340, Jalisco, MexicoGarcía-Cruz, D论文数: 0 引用数: 0 h-index: 0机构: Univ Guadalajara, Div Genet, Ctr Invest Biomed Occidente,CMNO,IMSS, Ctr Univ Ciencias Salud, Guadalajara 44340, Jalisco, Mexico Univ Guadalajara, Div Genet, Ctr Invest Biomed Occidente,CMNO,IMSS, Ctr Univ Ciencias Salud, Guadalajara 44340, Jalisco, Mexico
- [42] Lexical and gestural development in 5p deletion syndrome-A case reportJOURNAL OF COMMUNICATION DISORDERS, 2020, 83Kristoffersen, Kristian Emil论文数: 0 引用数: 0 h-index: 0机构: Nord Univ, N-8049 Bodo, Norway Frambu Resource Ctr Rare Disorders, N-14014 Siggerud, Norway Nord Univ, N-8049 Bodo, Norway
- [43] A case of 14q terminal deletion syndrome and hemifacial microsomia with review of terminal 14q deletion casesCLINICAL DYSMORPHOLOGY, 2024, 33 (02) : 90 - 94Kececi, Hayriye Nermin论文数: 0 引用数: 0 h-index: 0机构: Necmettin Erbakan Univ, Fac Med, Dept Pediat Genet, TR-42080 Meram, Konya, Turkiye Necmettin Erbakan Univ, Fac Med, Dept Pediat Genet, TR-42080 Meram, Konya, TurkiyeBasdemirci, Muserref论文数: 0 引用数: 0 h-index: 0机构: Konya City Hosp, Dept Med Genet, Med Genet, Konya, Turkiye Necmettin Erbakan Univ, Fac Med, Dept Pediat Genet, TR-42080 Meram, Konya, TurkiyeCaksen, Huseyin论文数: 0 引用数: 0 h-index: 0机构: Necmettin Erbakan Univ, Fac Med, Dept Pediat Genet, TR-42080 Meram, Konya, Turkiye Necmettin Erbakan Univ, Fac Med, Dept Pediat Genet, TR-42080 Meram, Konya, Turkiye
- [44] Confirmation of 6q21-6q22.1 Deletion in Acro-Cardio-Facial Syndrome and Further Delineation of This Contiguous Gene Deletion SyndromeAMERICAN JOURNAL OF MEDICAL GENETICS PART A, 2014, 164 (08) : 2109 - 2113Hudson, Cindy论文数: 0 引用数: 0 h-index: 0机构: Shodair Childrens Hosp, Dept Med Genet, Helena, MT 59604 USA Shodair Childrens Hosp, Dept Med Genet, Helena, MT 59604 USASchwanke, Corbin论文数: 0 引用数: 0 h-index: 0机构: Shodair Childrens Hosp, Dept Med Genet, Helena, MT 59604 USA Shodair Childrens Hosp, Dept Med Genet, Helena, MT 59604 USAJohnson, John P.论文数: 0 引用数: 0 h-index: 0机构: Shodair Childrens Hosp, Dept Med Genet, Helena, MT 59604 USA Shodair Childrens Hosp, Dept Med Genet, Helena, MT 59604 USAElias, Abdallah F.论文数: 0 引用数: 0 h-index: 0机构: Shodair Childrens Hosp, Dept Med Genet, Helena, MT 59604 USA Shodair Childrens Hosp, Dept Med Genet, Helena, MT 59604 USAPhillips, Sandy论文数: 0 引用数: 0 h-index: 0机构: Shodair Childrens Hosp, Dept Med Genet, Helena, MT 59604 USA Shodair Childrens Hosp, Dept Med Genet, Helena, MT 59604 USASchwalbe, Tammy论文数: 0 引用数: 0 h-index: 0机构: Shodair Childrens Hosp, Dept Med Genet, Helena, MT 59604 USA Shodair Childrens Hosp, Dept Med Genet, Helena, MT 59604 USATunby, Mary论文数: 0 引用数: 0 h-index: 0机构: Shodair Childrens Hosp, Dept Med Genet, Helena, MT 59604 USA Shodair Childrens Hosp, Dept Med Genet, Helena, MT 59604 USAXu, Dongbin论文数: 0 引用数: 0 h-index: 0机构: Shodair Childrens Hosp, Dept Med Genet, Helena, MT 59604 USA Shodair Childrens Hosp, Dept Med Genet, Helena, MT 59604 USA
- [45] Infantile Myelodysplastic Syndrome Associated with Pure Partial Trisomy 1q SyndromePEDIATRIC BLOOD & CANCER, 2017, 64 : S110 - S111Morokawa, Hirokazu论文数: 0 引用数: 0 h-index: 0机构: Shinshu Univ, Sch Med, Dept Pediat, Matsumoto, Nagano, Japan Shinshu Univ, Sch Med, Dept Pediat, Matsumoto, Nagano, JapanKamiya, Motoko论文数: 0 引用数: 0 h-index: 0机构: Shinshu Univ, Sch Med, Dept Pediat, Matsumoto, Nagano, Japan Shinshu Univ, Sch Med, Ctr Med Genet, Matsumoto, Nagano, Japan Shinshu Univ, Sch Med, Dept Pediat, Matsumoto, Nagano, JapanKomori, Kazutoshi论文数: 0 引用数: 0 h-index: 0机构: Shinshu Univ, Sch Med, Dept Pediat, Matsumoto, Nagano, Japan Shinshu Univ, Sch Med, Dept Pediat, Matsumoto, Nagano, JapanMorita, Daisuke论文数: 0 引用数: 0 h-index: 0机构: Shinshu Univ, Sch Med, Dept Pediat, Matsumoto, Nagano, Japan Shinshu Univ, Sch Med, Dept Pediat, Matsumoto, Nagano, JapanKurata, Takashi论文数: 0 引用数: 0 h-index: 0机构: Shinshu Univ, Sch Med, Dept Pediat, Matsumoto, Nagano, Japan Shinshu Univ, Sch Med, Dept Pediat, Matsumoto, Nagano, JapanTanaka, Miyuki论文数: 0 引用数: 0 h-index: 0机构: Shinshu Univ, Sch Med, Dept Pediat, Matsumoto, Nagano, Japan Shinshu Univ, Sch Med, Dept Pediat, Matsumoto, Nagano, JapanKosho, Tomoki论文数: 0 引用数: 0 h-index: 0机构: Shinshu Univ, Sch Med, Ctr Med Genet, Matsumoto, Nagano, Japan Shinshu Univ, Sch Med, Dept Pediat, Matsumoto, Nagano, JapanNakazawa, Yozo论文数: 0 引用数: 0 h-index: 0机构: Shinshu Univ, Sch Med, Dept Pediat, Matsumoto, Nagano, Japan Shinshu Univ, Sch Med, Dept Pediat, Matsumoto, Nagano, Japan
- [46] Metyrosine in psychosis associated with 22q11.2 deletion syndrome: Case reportJOURNAL OF CHILD AND ADOLESCENT PSYCHOPHARMACOLOGY, 2007, 17 (01) : 115 - 120Carandang, Carlo G.论文数: 0 引用数: 0 h-index: 0机构: Dalhousie Univ, 5850-5980 Univ Ave POB 9700, Halifax, NS B3K 6R8, Canada Dalhousie Univ, 5850-5980 Univ Ave POB 9700, Halifax, NS B3K 6R8, CanadaScholten, Monique C.论文数: 0 引用数: 0 h-index: 0机构: Dalhousie Univ, 5850-5980 Univ Ave POB 9700, Halifax, NS B3K 6R8, Canada
- [47] Additional case of Tsukahara's syndrome or new syndrome: Further delineation of the association of microcephaly and radio-ulnar synostosisAMERICAN JOURNAL OF MEDICAL GENETICS PART A, 2005, 132A (02) : 189 - 190Selicorni, A论文数: 0 引用数: 0 h-index: 0机构: 1 Clin Pediat, Clin Pediat De Marchi, I-20122 Milan, Italy 1 Clin Pediat, Clin Pediat De Marchi, I-20122 Milan, ItalyFerrarini, A论文数: 0 引用数: 0 h-index: 0机构: 1 Clin Pediat, Clin Pediat De Marchi, I-20122 Milan, Italy 1 Clin Pediat, Clin Pediat De Marchi, I-20122 Milan, ItalyCagnoli, G论文数: 0 引用数: 0 h-index: 0机构: 1 Clin Pediat, Clin Pediat De Marchi, I-20122 Milan, Italy 1 Clin Pediat, Clin Pediat De Marchi, I-20122 Milan, ItalyFratoni, A论文数: 0 引用数: 0 h-index: 0机构: 1 Clin Pediat, Clin Pediat De Marchi, I-20122 Milan, Italy 1 Clin Pediat, Clin Pediat De Marchi, I-20122 Milan, ItalyBottigelli, M论文数: 0 引用数: 0 h-index: 0机构: 1 Clin Pediat, Clin Pediat De Marchi, I-20122 Milan, Italy 1 Clin Pediat, Clin Pediat De Marchi, I-20122 Milan, ItalyMilani, D论文数: 0 引用数: 0 h-index: 0机构: 1 Clin Pediat, Clin Pediat De Marchi, I-20122 Milan, Italy 1 Clin Pediat, Clin Pediat De Marchi, I-20122 Milan, Italy
- [48] Further delineation of the NTHL1 associated syndrome: a report from the French oncogenetic consortiumEUROPEAN JOURNAL OF HUMAN GENETICS, 2020, 28 (SUPPL 1) : 543 - 543Boulouard, F.论文数: 0 引用数: 0 h-index: 0机构: Normandie Univ, UNIROUEN, CHU Rouen, Ctr Normand Genom & Med Personnalisee,Dept Genet, Rouen, France Normandie Univ, UNIROUEN, CHU Rouen, Inserm,U1245, Rouen, France Ctr Francois Bacles, Lab Genet Mol, Caen, France Normandie Univ, UNIROUEN, CHU Rouen, Ctr Normand Genom & Med Personnalisee,Dept Genet, Rouen, FranceKasper, E.论文数: 0 引用数: 0 h-index: 0机构: Normandie Univ, UNIROUEN, CHU Rouen, Ctr Normand Genom & Med Personnalisee,Dept Genet, Rouen, France Normandie Univ, UNIROUEN, CHU Rouen, Inserm,U1245, Rouen, France Normandie Univ, UNIROUEN, CHU Rouen, Ctr Normand Genom & Med Personnalisee,Dept Genet, Rouen, FranceBuisine, M.论文数: 0 引用数: 0 h-index: 0机构: Univ Lille, CHU Lille, INSERM, UMR S 1172,Inst Biochim & Biol Mol,Oncogenet Mol, Lille, France Normandie Univ, UNIROUEN, CHU Rouen, Ctr Normand Genom & Med Personnalisee,Dept Genet, Rouen, FranceLienard, G.论文数: 0 引用数: 0 h-index: 0机构: Normandie Univ, UNIROUEN, CHU Rouen, Ctr Normand Genom & Med Personnalisee,Dept Genet, Rouen, France Normandie Univ, UNIROUEN, CHU Rouen, Inserm,U1245, Rouen, France Normandie Univ, UNIROUEN, CHU Rouen, Ctr Normand Genom & Med Personnalisee,Dept Genet, Rouen, FranceVasseur, S.论文数: 0 引用数: 0 h-index: 0机构: Normandie Univ, UNIROUEN, CHU Rouen, Ctr Normand Genom & Med Personnalisee,Dept Genet, Rouen, France Normandie Univ, UNIROUEN, CHU Rouen, Inserm,U1245, Rouen, France Normandie Univ, UNIROUEN, CHU Rouen, Ctr Normand Genom & Med Personnalisee,Dept Genet, Rouen, FranceManase, S.论文数: 0 引用数: 0 h-index: 0机构: Normandie Univ, UNIROUEN, CHU Rouen, Ctr Normand Genom & Med Personnalisee,Dept Genet, Rouen, France Normandie Univ, UNIROUEN, CHU Rouen, Inserm,U1245, Rouen, France Normandie Univ, UNIROUEN, CHU Rouen, Ctr Normand Genom & Med Personnalisee,Dept Genet, Rouen, FranceBahuau, M.论文数: 0 引用数: 0 h-index: 0机构: CHU Henri Mondor, Dept Biochim Biol Mol, Pharmacol, Genet Med, Creteil, France Normandie Univ, UNIROUEN, CHU Rouen, Ctr Normand Genom & Med Personnalisee,Dept Genet, Rouen, FranceBubien, V.论文数: 0 引用数: 0 h-index: 0机构: CLCC Inst Bergonie, Lab Genet Mol, Dept BioPathol, Unite Oncogenet, Bordeaux, France Normandie Univ, UNIROUEN, CHU Rouen, Ctr Normand Genom & Med Personnalisee,Dept Genet, Rouen, FranceCoulet, F.论文数: 0 引用数: 0 h-index: 0机构: Charles Foix Hop Pitie Salpetriere, CHU Paris GH Pitie Salpetriere, UF Oncogenet & Angiogenet Mol, Dept Genet, Paris, France Normandie Univ, UNIROUEN, CHU Rouen, Ctr Normand Genom & Med Personnalisee,Dept Genet, Rouen, FranceCusin, V.论文数: 0 引用数: 0 h-index: 0机构: Charles Foix Hop Pitie Salpetriere, CHU Paris GH Pitie Salpetriere, Dept Genet, Paris, France Normandie Univ, UNIROUEN, CHU Rouen, Ctr Normand Genom & Med Personnalisee,Dept Genet, Rouen, FranceDhooge, M.论文数: 0 引用数: 0 h-index: 0机构: Hop Cochin, CHU Paris Ctr, Serv Gastroenterol, Site Cochin, Paris, France Normandie Univ, UNIROUEN, CHU Rouen, Ctr Normand Genom & Med Personnalisee,Dept Genet, Rouen, FranceGolmard, L.论文数: 0 引用数: 0 h-index: 0机构: PSL Res Univ, CLCC Inst Curie, Unite Genet Constitut, Serv Genet, Paris, France Normandie Univ, UNIROUEN, CHU Rouen, Ctr Normand Genom & Med Personnalisee,Dept Genet, Rouen, FranceGoussot, V.论文数: 0 引用数: 0 h-index: 0机构: CLCC Georges Francois Leclerc, Dept Biol & Pathol Tumeurs, Dijon, France Normandie Univ, UNIROUEN, CHU Rouen, Ctr Normand Genom & Med Personnalisee,Dept Genet, Rouen, FranceHamzaoui, N.论文数: 0 引用数: 0 h-index: 0机构: Hop Cochin, CHU Paris Ctr, Lab Oncogenet, Site Cochin, Paris, France Normandie Univ, UNIROUEN, CHU Rouen, Ctr Normand Genom & Med Personnalisee,Dept Genet, Rouen, FranceLacaze, E.论文数: 0 引用数: 0 h-index: 0机构: Normandie Univ, UNIROUEN, CHU Rouen, Ctr Normand Genom & Med Personnalisee,Dept Genet, Rouen, FranceLejeune, S.论文数: 0 引用数: 0 h-index: 0机构: Hop Jeanne de Flandre, CHU Lille, Pole Biol Pathol Genet, Clin Genet Guy Fontaine, Lille, France Normandie Univ, UNIROUEN, CHU Rouen, Ctr Normand Genom & Med Personnalisee,Dept Genet, Rouen, FranceMauillon, J.论文数: 0 引用数: 0 h-index: 0机构: Normandie Univ, UNIROUEN, CHU Rouen, Ctr Normand Genom & Med Personnalisee,Dept Genet, Rouen, France Normandie Univ, UNIROUEN, CHU Rouen, Inserm,U1245, Rouen, France Normandie Univ, UNIROUEN, CHU Rouen, Ctr Normand Genom & Med Personnalisee,Dept Genet, Rouen, FrancePinson, S.论文数: 0 引用数: 0 h-index: 0机构: CHU Lyon HCL GH Est, Unite Med Genet Canc & Malad Multifactorielles, Serv Genet & Mol Clin, Lyon, France Normandie Univ, UNIROUEN, CHU Rouen, Ctr Normand Genom & Med Personnalisee,Dept Genet, Rouen, FranceTlemsani, C.论文数: 0 引用数: 0 h-index: 0机构: CHU Paris Ctr, Hop Cochin, Serv Cancerol, Site Cochin, Paris, France Normandie Univ, UNIROUEN, CHU Rouen, Ctr Normand Genom & Med Personnalisee,Dept Genet, Rouen, FranceToulas, C.论文数: 0 引用数: 0 h-index: 0机构: Inst Univ Canc Toulouse Oncopole, Lab Oncogenet, Toulouse, France Normandie Univ, UNIROUEN, CHU Rouen, Ctr Normand Genom & Med Personnalisee,Dept Genet, Rouen, FranceRey, J.论文数: 0 引用数: 0 h-index: 0机构: CHU Montpellier, Hop Arnaud Villeneuve, Lab Biol Tumeurs Solides, Montpellier, France Normandie Univ, UNIROUEN, CHU Rouen, Ctr Normand Genom & Med Personnalisee,Dept Genet, Rouen, FranceUhrhammer, N.论文数: 0 引用数: 0 h-index: 0机构: CLCC Jean Perrin, Lab Biol Med OncoGenAuvergne, Clermont Ferrand, France Normandie Univ, UNIROUEN, CHU Rouen, Ctr Normand Genom & Med Personnalisee,Dept Genet, Rouen, FranceBougeard-Denoyelle, G.论文数: 0 引用数: 0 h-index: 0机构: Normandie Univ, UNIROUEN, CHU Rouen, Ctr Normand Genom & Med Personnalisee,Dept Genet, Rouen, France Normandie Univ, UNIROUEN, CHU Rouen, Inserm,U1245, Rouen, France Normandie Univ, UNIROUEN, CHU Rouen, Ctr Normand Genom & Med Personnalisee,Dept Genet, Rouen, FranceFrebourg, T.论文数: 0 引用数: 0 h-index: 0机构: Normandie Univ, UNIROUEN, CHU Rouen, Ctr Normand Genom & Med Personnalisee,Dept Genet, Rouen, France Normandie Univ, UNIROUEN, CHU Rouen, Inserm,U1245, Rouen, France Normandie Univ, UNIROUEN, CHU Rouen, Ctr Normand Genom & Med Personnalisee,Dept Genet, Rouen, FranceHoudayer, C.论文数: 0 引用数: 0 h-index: 0机构: Normandie Univ, UNIROUEN, CHU Rouen, Ctr Normand Genom & Med Personnalisee,Dept Genet, Rouen, France Normandie Univ, UNIROUEN, CHU Rouen, Inserm,U1245, Rouen, France Normandie Univ, UNIROUEN, CHU Rouen, Ctr Normand Genom & Med Personnalisee,Dept Genet, Rouen, FranceBaert-Desurmont, S.论文数: 0 引用数: 0 h-index: 0机构: Normandie Univ, UNIROUEN, CHU Rouen, Ctr Normand Genom & Med Personnalisee,Dept Genet, Rouen, France Normandie Univ, UNIROUEN, CHU Rouen, Inserm,U1245, Rouen, France Normandie Univ, UNIROUEN, CHU Rouen, Ctr Normand Genom & Med Personnalisee,Dept Genet, Rouen, France
- [49] Further delineation of the NTHL1 associated syndrome: A report from the French Oncogenetic ConsortiumCLINICAL GENETICS, 2021, 99 (05) : 662 - 672Boulouard, Flavie论文数: 0 引用数: 0 h-index: 0机构: Normandie Univ, Inserm U1245, Normandy Ctr Genom & Personalized Med, UNIROUEN,Dept Genet, Rouen, France Rouen Univ Hosp, Rouen, France Comprehens Canc Ctr Francois Baclesse, Lab Canc Biol & Genet, Caen, France Normandie Univ, Inserm U1245, Normandy Ctr Genom & Personalized Med, UNIROUEN,Dept Genet, Rouen, FranceKasper, Edwige论文数: 0 引用数: 0 h-index: 0机构: Normandie Univ, Inserm U1245, Normandy Ctr Genom & Personalized Med, UNIROUEN,Dept Genet, Rouen, France Rouen Univ Hosp, Rouen, France Normandie Univ, Inserm U1245, Normandy Ctr Genom & Personalized Med, UNIROUEN,Dept Genet, Rouen, FranceBuisine, Marie-Pierre论文数: 0 引用数: 0 h-index: 0机构: Lille Univ, Lille Univ Hosp Ctr, Dept Biochem & Mol Biol, UMR 1277,Inserm 9020,CNRS, Lille, France Normandie Univ, Inserm U1245, Normandy Ctr Genom & Personalized Med, UNIROUEN,Dept Genet, Rouen, FranceLienard, Gwendoline论文数: 0 引用数: 0 h-index: 0机构: Normandie Univ, Inserm U1245, Normandy Ctr Genom & Personalized Med, UNIROUEN,Dept Genet, Rouen, France Rouen Univ Hosp, Rouen, France Normandie Univ, Inserm U1245, Normandy Ctr Genom & Personalized Med, UNIROUEN,Dept Genet, Rouen, FranceVasseur, Stephanie论文数: 0 引用数: 0 h-index: 0机构: Normandie Univ, Inserm U1245, Normandy Ctr Genom & Personalized Med, UNIROUEN,Dept Genet, Rouen, France Rouen Univ Hosp, Rouen, France Normandie Univ, Inserm U1245, Normandy Ctr Genom & Personalized Med, UNIROUEN,Dept Genet, Rouen, FranceManase, Sandrine论文数: 0 引用数: 0 h-index: 0机构: Normandie Univ, Inserm U1245, Normandy Ctr Genom & Personalized Med, UNIROUEN,Dept Genet, Rouen, France Rouen Univ Hosp, Rouen, France Normandie Univ, Inserm U1245, Normandy Ctr Genom & Personalized Med, UNIROUEN,Dept Genet, Rouen, FranceBahuau, Michel论文数: 0 引用数: 0 h-index: 0机构: Henri Mondor Hosp, Med Genet Dept, Creteil, France Normandie Univ, Inserm U1245, Normandy Ctr Genom & Personalized Med, UNIROUEN,Dept Genet, Rouen, FranceSimonet, Emmanuelle Barouk论文数: 0 引用数: 0 h-index: 0机构: Inst Bergonie, Canc Genet Unit, Bordeaux, France Normandie Univ, Inserm U1245, Normandy Ctr Genom & Personalized Med, UNIROUEN,Dept Genet, Rouen, FranceBubien, Virginie论文数: 0 引用数: 0 h-index: 0机构: Inst Bergonie, Canc Genet Unit, Bordeaux, France Normandie Univ, Inserm U1245, Normandy Ctr Genom & Personalized Med, UNIROUEN,Dept Genet, Rouen, FranceCoulet, Florence论文数: 0 引用数: 0 h-index: 0机构: Hop Univ Pitie Salpetriere Charles Foix, Dept Genet, Paris, France Normandie Univ, Inserm U1245, Normandy Ctr Genom & Personalized Med, UNIROUEN,Dept Genet, Rouen, FranceCusin, Veronica论文数: 0 引用数: 0 h-index: 0机构: Hop Univ Pitie Salpetriere Charles Foix, Dept Genet, Paris, France Normandie Univ, Inserm U1245, Normandy Ctr Genom & Personalized Med, UNIROUEN,Dept Genet, Rouen, FranceDhooge, Marion论文数: 0 引用数: 0 h-index: 0机构: Paris Descartes Univ, Cochin Univ Hosp, Gastroenterol Unit, Paris, France Normandie Univ, Inserm U1245, Normandy Ctr Genom & Personalized Med, UNIROUEN,Dept Genet, Rouen, FranceGolmard, Lisa论文数: 0 引用数: 0 h-index: 0机构: Lettres Res Univ, Inst Curie, Dept Genet & Paris Sci, Paris, France Normandie Univ, Inserm U1245, Normandy Ctr Genom & Personalized Med, UNIROUEN,Dept Genet, Rouen, FranceGoussot, Vincent论文数: 0 引用数: 0 h-index: 0机构: Georges Francois Leclerc Ctr, Dept Tumor Biol & Pathol, Dijon, France Normandie Univ, Inserm U1245, Normandy Ctr Genom & Personalized Med, UNIROUEN,Dept Genet, Rouen, FranceHamzaoui, Nadim论文数: 0 引用数: 0 h-index: 0机构: Hop Cochin, AP HP, Dept Oncogenet, Paris, France Normandie Univ, Inserm U1245, Normandy Ctr Genom & Personalized Med, UNIROUEN,Dept Genet, Rouen, FranceLacaze, Elodie论文数: 0 引用数: 0 h-index: 0机构: Le Havre Gen Hosp, Normandy Ctr Genom & Personalized Med, Dept Genet, Le Havre, France Normandie Univ, Inserm U1245, Normandy Ctr Genom & Personalized Med, UNIROUEN,Dept Genet, Rouen, FranceLejeune, Sophie论文数: 0 引用数: 0 h-index: 0机构: Lille Univ Hosp Ctr, Jeanne de Flandre Hosp, Genet Pathol Biol Dept, Lille, France Normandie Univ, Inserm U1245, Normandy Ctr Genom & Personalized Med, UNIROUEN,Dept Genet, Rouen, FranceMauillon, Jacques论文数: 0 引用数: 0 h-index: 0机构: Normandie Univ, Inserm U1245, Normandy Ctr Genom & Personalized Med, UNIROUEN,Dept Genet, Rouen, France Rouen Univ Hosp, Rouen, France Normandie Univ, Inserm U1245, Normandy Ctr Genom & Personalized Med, UNIROUEN,Dept Genet, Rouen, FranceBeaumont, Marie-Pascale论文数: 0 引用数: 0 h-index: 0机构: Rennes Univ Hosp Ctr, Dept Genet, Rennes, France Normandie Univ, Inserm U1245, Normandy Ctr Genom & Personalized Med, UNIROUEN,Dept Genet, Rouen, FrancePinson, Stephane论文数: 0 引用数: 0 h-index: 0机构: Hosp Civils LYON HCL, Univ Hosp, East Pathol Ctr, Genet Dept, Bron, France Normandie Univ, Inserm U1245, Normandy Ctr Genom & Personalized Med, UNIROUEN,Dept Genet, Rouen, FranceTlemsani, Camille论文数: 0 引用数: 0 h-index: 0机构: Hop Cochin, AP HP, Dept Oncogenet, Paris, France Normandie Univ, Inserm U1245, Normandy Ctr Genom & Personalized Med, UNIROUEN,Dept Genet, Rouen, FranceToulas, Christine论文数: 0 引用数: 0 h-index: 0机构: Canc Univ Inst Toulouse Oncopole, Oncogenet Lab, Toulouse, France Normandie Univ, Inserm U1245, Normandy Ctr Genom & Personalized Med, UNIROUEN,Dept Genet, Rouen, FranceRey, Jean-Marc论文数: 0 引用数: 0 h-index: 0机构: Montpellier Univ Hosp, Dept Pathol & Oncobiol, Montpellier, France Normandie Univ, Inserm U1245, Normandy Ctr Genom & Personalized Med, UNIROUEN,Dept Genet, Rouen, FranceUhrhammer, Nancy论文数: 0 引用数: 0 h-index: 0机构: Ctr Jean Perrin, Oncogenet, Clermont Ferrand, France Clermont Auvergne Univ, INSERM U1240, Clermont Ferrand, France Normandie Univ, Inserm U1245, Normandy Ctr Genom & Personalized Med, UNIROUEN,Dept Genet, Rouen, FranceBougeard, Gaelle论文数: 0 引用数: 0 h-index: 0机构: Normandie Univ, Inserm U1245, Normandy Ctr Genom & Personalized Med, UNIROUEN,Dept Genet, Rouen, France Rouen Univ Hosp, Rouen, France Normandie Univ, Inserm U1245, Normandy Ctr Genom & Personalized Med, UNIROUEN,Dept Genet, Rouen, France论文数: 引用数: h-index:机构:论文数: 引用数: h-index:机构:Baert-Desurmont, Stephanie论文数: 0 引用数: 0 h-index: 0机构: Normandie Univ, Inserm U1245, Normandy Ctr Genom & Personalized Med, UNIROUEN,Dept Genet, Rouen, France Rouen Univ Hosp, Rouen, France Normandie Univ, Inserm U1245, Normandy Ctr Genom & Personalized Med, UNIROUEN,Dept Genet, Rouen, France
- [50] A child with an inherited 0.31 Mb microdeletion of chromosome 14q32.33: Further delineation of a critical region for the 14q32 deletion syndromeAMERICAN JOURNAL OF MEDICAL GENETICS PART A, 2012, 158A (08) : 1962 - 1966Holder, J. Lloyd, Jr.论文数: 0 引用数: 0 h-index: 0机构: Texas Childrens Hosp, Houston, TX 77030 USA Baylor Coll Med, Dept Pediat, Div Child Neurol, Houston, TX 77030 USA Texas Childrens Hosp, Houston, TX 77030 USALotze, Timothy E.论文数: 0 引用数: 0 h-index: 0机构: Texas Childrens Hosp, Houston, TX 77030 USA Baylor Coll Med, Dept Pediat, Div Child Neurol, Houston, TX 77030 USA Texas Childrens Hosp, Houston, TX 77030 USABacino, Carlos论文数: 0 引用数: 0 h-index: 0机构: Texas Childrens Hosp, Houston, TX 77030 USA Baylor Coll Med, Dept Mol & Human Genet, Houston, TX 77030 USA Texas Childrens Hosp, Houston, TX 77030 USACheung, Sau-Wai论文数: 0 引用数: 0 h-index: 0机构: Baylor Coll Med, Dept Mol & Human Genet, Houston, TX 77030 USA Texas Childrens Hosp, Houston, TX 77030 USA