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- [1] Oral Manifestations of Wolf-Hirschhorn Syndrome: Genotype-Phenotype Correlation AnalysisJOURNAL OF CLINICAL MEDICINE, 2020, 9 (11) : 1 - 14Limeres, Jacobo论文数: 0 引用数: 0 h-index: 0机构: Univ Santiago Compostela USC, Hlth Res Inst Santiago de Compostela IDIS, Med Surg Dent Res Grp OMEQUI, Santiago De Compostela 15782, Spain Univ Santiago Compostela USC, Hlth Res Inst Santiago de Compostela IDIS, Med Surg Dent Res Grp OMEQUI, Santiago De Compostela 15782, SpainSerrano, Candela论文数: 0 引用数: 0 h-index: 0机构: Univ Santiago Compostela USC, Hlth Res Inst Santiago de Compostela IDIS, Med Surg Dent Res Grp OMEQUI, Santiago De Compostela 15782, Spain Univ Santiago Compostela USC, Hlth Res Inst Santiago de Compostela IDIS, Med Surg Dent Res Grp OMEQUI, Santiago De Compostela 15782, SpainDe Nova, Joaquin Manuel论文数: 0 引用数: 0 h-index: 0机构: Univ Complutense Madrid, Sch Dent, Dept Stomatol 4, Madrid 28040, Spain Univ Hosp Doctor Peset FISABIO, Dept Stomatol, Valencia 46017, Spain Univ Santiago Compostela USC, Hlth Res Inst Santiago de Compostela IDIS, Med Surg Dent Res Grp OMEQUI, Santiago De Compostela 15782, SpainSilvestre-Rangil, Javier论文数: 0 引用数: 0 h-index: 0机构: Univ Hosp Doctor Peset FISABIO, Dept Stomatol, Valencia 46017, Spain Univ Santiago Compostela USC, Hlth Res Inst Santiago de Compostela IDIS, Med Surg Dent Res Grp OMEQUI, Santiago De Compostela 15782, SpainMachuca, Guillermo论文数: 0 引用数: 0 h-index: 0机构: Univ Seville, Sch Dent, Dept Special Care Dent, Seville 41009, Spain Univ Santiago Compostela USC, Hlth Res Inst Santiago de Compostela IDIS, Med Surg Dent Res Grp OMEQUI, Santiago De Compostela 15782, SpainMaura, Isabel论文数: 0 引用数: 0 h-index: 0机构: Univ Barcelona, Serv Pediat Dent, Childrens Hosp HM Nens, Barcelona 08009, Spain Univ Santiago Compostela USC, Hlth Res Inst Santiago de Compostela IDIS, Med Surg Dent Res Grp OMEQUI, Santiago De Compostela 15782, SpainCruz Ruiz-Villandiego, Jose论文数: 0 引用数: 0 h-index: 0机构: Quiron Hosp, Serv Special Care Dent, San Sebastian 200012, Spain Univ Santiago Compostela USC, Hlth Res Inst Santiago de Compostela IDIS, Med Surg Dent Res Grp OMEQUI, Santiago De Compostela 15782, SpainDiz, Pedro论文数: 0 引用数: 0 h-index: 0机构: Univ Santiago Compostela USC, Hlth Res Inst Santiago de Compostela IDIS, Med Surg Dent Res Grp OMEQUI, Santiago De Compostela 15782, Spain Univ Santiago Compostela USC, Hlth Res Inst Santiago de Compostela IDIS, Med Surg Dent Res Grp OMEQUI, Santiago De Compostela 15782, SpainBlanco-Lago, Raquel论文数: 0 引用数: 0 h-index: 0机构: Univ Hosp Cent Asturias, Serv Neuropediat, Oviedo 33011, Spain Univ Santiago Compostela USC, Hlth Res Inst Santiago de Compostela IDIS, Med Surg Dent Res Grp OMEQUI, Santiago De Compostela 15782, SpainNevado, Julian论文数: 0 引用数: 0 h-index: 0机构: La Paz Univ Hosp, Med & Mol Genet Inst INGEMM, IdiPAZ, Madrid 28046, Spain Inst Salud Carlos III, Inst Rare Dis Res IIER, Madrid 28029, Spain Inst Salud Carlos III, Ctr Biomed Network Res Rare Dis CIBERER, Madrid 28029, Spain La Paz Univ Hosp, ITHACA, ERN, Madrid 28046, Spain Univ Santiago Compostela USC, Hlth Res Inst Santiago de Compostela IDIS, Med Surg Dent Res Grp OMEQUI, Santiago De Compostela 15782, SpainDiniz-Freitas, Marcio论文数: 0 引用数: 0 h-index: 0机构: Univ Santiago Compostela USC, Hlth Res Inst Santiago de Compostela IDIS, Med Surg Dent Res Grp OMEQUI, Santiago De Compostela 15782, Spain Univ Santiago Compostela USC, Hlth Res Inst Santiago de Compostela IDIS, Med Surg Dent Res Grp OMEQUI, Santiago De Compostela 15782, Spain
- [2] On the Nosology and Pathogenesis of Wolf-Hirschhorn Syndrome: Genotype-Phenotype Correlation Analysis of 80 Patients and Literature ReviewAMERICAN JOURNAL OF MEDICAL GENETICS PART C-SEMINARS IN MEDICAL GENETICS, 2008, 148C (04) : 257 - 269Zollino, Marcella论文数: 0 引用数: 0 h-index: 0机构: Univ Cattolica Sacro Cuore, Ist Genet Med, Policlin A Gemelli, Dept Med Genet, I-00168 Rome, Italy Univ Cattolica Sacro Cuore, Ist Genet Med, Policlin A Gemelli, Dept Med Genet, I-00168 Rome, ItalyMurdolo, Marina论文数: 0 引用数: 0 h-index: 0机构: Univ Cattolica Sacro Cuore, Ist Genet Med, Policlin A Gemelli, Dept Med Genet, I-00168 Rome, ItalyMarangi, Giuseppe论文数: 0 引用数: 0 h-index: 0机构: Univ Cattolica Sacro Cuore, Ist Genet Med, Policlin A Gemelli, Dept Med Genet, I-00168 Rome, ItalyPecile, Vanna论文数: 0 引用数: 0 h-index: 0机构: IRCCS Burlo Garofalo, Trieste, Italy Univ Cattolica Sacro Cuore, Ist Genet Med, Policlin A Gemelli, Dept Med Genet, I-00168 Rome, ItalyGalasso, Cinzia论文数: 0 引用数: 0 h-index: 0机构: Univ Tor Vergata, Paediat Neurol Unit, Dept Neurosci, Rome, Italy Univ Cattolica Sacro Cuore, Ist Genet Med, Policlin A Gemelli, Dept Med Genet, I-00168 Rome, ItalyMazzanti, Laura论文数: 0 引用数: 0 h-index: 0机构: Univ Bologna, Dept Obstet Gynecol & Paediat, I-40126 Bologna, Italy Univ Cattolica Sacro Cuore, Ist Genet Med, Policlin A Gemelli, Dept Med Genet, I-00168 Rome, ItalyNeri, Giovanni论文数: 0 引用数: 0 h-index: 0机构: Univ Cattolica Sacro Cuore, Ist Genet Med, Policlin A Gemelli, Dept Med Genet, I-00168 Rome, Italy
- [3] Genotype-phenotype correlations and clinical diagnostic criteria in Wolf-Hirschhorn syndromeAMERICAN JOURNAL OF MEDICAL GENETICS, 2000, 94 (03): : 254 - 261Zollino, M论文数: 0 引用数: 0 h-index: 0机构: Univ Cattolica Sacro Cuore, Ist Genet Med, Fac Med A Gemelli, I-00168 Rome, ItalyDi Stefano, C论文数: 0 引用数: 0 h-index: 0机构: Univ Cattolica Sacro Cuore, Ist Genet Med, Fac Med A Gemelli, I-00168 Rome, ItalyZampino, G论文数: 0 引用数: 0 h-index: 0机构: Univ Cattolica Sacro Cuore, Ist Genet Med, Fac Med A Gemelli, I-00168 Rome, ItalyMastroiacovo, P论文数: 0 引用数: 0 h-index: 0机构: Univ Cattolica Sacro Cuore, Ist Genet Med, Fac Med A Gemelli, I-00168 Rome, ItalyWright, TJ论文数: 0 引用数: 0 h-index: 0机构: Univ Cattolica Sacro Cuore, Ist Genet Med, Fac Med A Gemelli, I-00168 Rome, ItalySorge, G论文数: 0 引用数: 0 h-index: 0机构: Univ Cattolica Sacro Cuore, Ist Genet Med, Fac Med A Gemelli, I-00168 Rome, ItalySelicorni, A论文数: 0 引用数: 0 h-index: 0机构: Univ Cattolica Sacro Cuore, Ist Genet Med, Fac Med A Gemelli, I-00168 Rome, ItalyTenconi, R论文数: 0 引用数: 0 h-index: 0机构: Univ Cattolica Sacro Cuore, Ist Genet Med, Fac Med A Gemelli, I-00168 Rome, ItalyZappalà, A论文数: 0 引用数: 0 h-index: 0机构: Univ Cattolica Sacro Cuore, Ist Genet Med, Fac Med A Gemelli, I-00168 Rome, ItalyBattaglia, A论文数: 0 引用数: 0 h-index: 0机构: Univ Cattolica Sacro Cuore, Ist Genet Med, Fac Med A Gemelli, I-00168 Rome, ItalyDi Rocco, M论文数: 0 引用数: 0 h-index: 0机构: Univ Cattolica Sacro Cuore, Ist Genet Med, Fac Med A Gemelli, I-00168 Rome, ItalyPalka, G论文数: 0 引用数: 0 h-index: 0机构: Univ Cattolica Sacro Cuore, Ist Genet Med, Fac Med A Gemelli, I-00168 Rome, ItalyPallotta, R论文数: 0 引用数: 0 h-index: 0机构: Univ Cattolica Sacro Cuore, Ist Genet Med, Fac Med A Gemelli, I-00168 Rome, ItalyAltherr, MR论文数: 0 引用数: 0 h-index: 0机构: Univ Cattolica Sacro Cuore, Ist Genet Med, Fac Med A Gemelli, I-00168 Rome, ItalyNeri, G论文数: 0 引用数: 0 h-index: 0机构: Univ Cattolica Sacro Cuore, Ist Genet Med, Fac Med A Gemelli, I-00168 Rome, Italy
- [4] Disorders of sex development in Wolf-Hirschhorn syndrome: a genotype-phenotype correlation and MSX1 as candidate geneMOLECULAR CYTOGENETICS, 2021, 14 (01)论文数: 引用数: h-index:机构:Ayech, Hedia论文数: 0 引用数: 0 h-index: 0机构: Farhat Hached Univ, Pediat Dept, Teaching Hosp, Sousse, Tunisia Farhat Hached Univ, Teaching Hosp, Lab Human Cytogenet Mol Genet & Biol Reprod, Sousse, TunisiaKraiem, Olfa论文数: 0 引用数: 0 h-index: 0机构: Reg Hosp, Pediat Dept, Kairouan, Tunisia Farhat Hached Univ, Teaching Hosp, Lab Human Cytogenet Mol Genet & Biol Reprod, Sousse, Tunisia论文数: 引用数: h-index:机构:Jelloul, Afef论文数: 0 引用数: 0 h-index: 0机构: Farhat Hached Univ, Teaching Hosp, Lab Human Cytogenet Mol Genet & Biol Reprod, Sousse, Tunisia Farhat Hached Univ, Teaching Hosp, Lab Human Cytogenet Mol Genet & Biol Reprod, Sousse, TunisiaBen Hadj Hmida, Imen论文数: 0 引用数: 0 h-index: 0机构: Farhat Hached Univ, Teaching Hosp, Lab Human Cytogenet Mol Genet & Biol Reprod, Sousse, Tunisia Farhat Hached Univ, Teaching Hosp, Lab Human Cytogenet Mol Genet & Biol Reprod, Sousse, TunisiaMahdhaoui, Nabiha论文数: 0 引用数: 0 h-index: 0机构: Farhat Hached Univ, Pediat Dept, Teaching Hosp, Sousse, Tunisia Farhat Hached Univ, Teaching Hosp, Lab Human Cytogenet Mol Genet & Biol Reprod, Sousse, TunisiaSaad, Ali论文数: 0 引用数: 0 h-index: 0机构: Farhat Hached Univ, Teaching Hosp, Lab Human Cytogenet Mol Genet & Biol Reprod, Sousse, Tunisia Univ Sousse, Fac Med Sousse, Unite Serv Communs Genet Humaine, Sousse, Tunisia Farhat Hached Univ, Teaching Hosp, Lab Human Cytogenet Mol Genet & Biol Reprod, Sousse, TunisiaMougou-Zerelli, Soumaya论文数: 0 引用数: 0 h-index: 0机构: Farhat Hached Univ, Teaching Hosp, Lab Human Cytogenet Mol Genet & Biol Reprod, Sousse, Tunisia Univ Sousse, Fac Med Sousse, Unite Serv Communs Genet Humaine, Sousse, Tunisia Farhat Hached Univ, Teaching Hosp, Lab Human Cytogenet Mol Genet & Biol Reprod, Sousse, Tunisia
- [5] Microarray and FISH-Based Genotype-Phenotype Analysis of 22 Japanese Patients With Wolf-Hirschhorn SyndromeAMERICAN JOURNAL OF MEDICAL GENETICS PART A, 2014, 164 (03) : 597 - 609Shimizu, Kenji论文数: 0 引用数: 0 h-index: 0机构: Shinshu Univ, Sch Med, Dept Med Genet, Matsumoto, Nagano 3908621, Japan Saitama Childrens Med Ctr, Div Med Genet, Saitama, Japan Shinshu Univ, Sch Med, Dept Med Genet, Matsumoto, Nagano 3908621, JapanWakui, Keiko论文数: 0 引用数: 0 h-index: 0机构: Shinshu Univ, Sch Med, Dept Med Genet, Matsumoto, Nagano 3908621, Japan Shinshu Univ, Sch Med, Dept Med Genet, Matsumoto, Nagano 3908621, JapanKosho, Tomoki论文数: 0 引用数: 0 h-index: 0机构: Shinshu Univ, Sch Med, Dept Med Genet, Matsumoto, Nagano 3908621, Japan Shinshu Univ, Sch Med, Dept Med Genet, Matsumoto, Nagano 3908621, JapanOkamoto, Nobuhiko论文数: 0 引用数: 0 h-index: 0机构: Osaka Med Ctr, Dept Med Genet, Osaka, Japan Res Inst Maternal & Child Hlth, Osaka, Japan Shinshu Univ, Sch Med, Dept Med Genet, Matsumoto, Nagano 3908621, JapanMizuno, Seiji论文数: 0 引用数: 0 h-index: 0机构: Cent Hosp Kasugai, Aichi Human Serv Ctr, Dept Pediat, Kasugai, Aichi, Japan Shinshu Univ, Sch Med, Dept Med Genet, Matsumoto, Nagano 3908621, JapanItomi, Kazuya论文数: 0 引用数: 0 h-index: 0机构: Aichi Childrens Hlth & Med Ctr, Dept Pediat Neurol, Obu, Aichi, Japan Shinshu Univ, Sch Med, Dept Med Genet, Matsumoto, Nagano 3908621, JapanHattori, Shigeto论文数: 0 引用数: 0 h-index: 0机构: Gunma Univ Hosp, Dept Pediat, Maebashi, Gunma, Japan Shinshu Univ, Sch Med, Dept Med Genet, Matsumoto, Nagano 3908621, JapanNishio, Kimio论文数: 0 引用数: 0 h-index: 0机构: Seirei Hamamatsu Gen Hosp, Dept Neonatol, Hamamatsu, Shizuoka, Japan Shinshu Univ, Sch Med, Dept Med Genet, Matsumoto, Nagano 3908621, JapanSamura, Osamu论文数: 0 引用数: 0 h-index: 0机构: NHO Kure Med Ctr, Dept Obstet & Gynecol, Kure, Japan Chugoku Canc Ctr, Kure, Japan Shinshu Univ, Sch Med, Dept Med Genet, Matsumoto, Nagano 3908621, JapanKobayashi, Yoshiyuki论文数: 0 引用数: 0 h-index: 0机构: Hiroshima Univ Hosp, Dept Pediat, Hiroshima, Japan Shinshu Univ, Sch Med, Dept Med Genet, Matsumoto, Nagano 3908621, JapanKako, Yuko论文数: 0 引用数: 0 h-index: 0机构: Showa Univ, Sch Med, Dept Pediat, Tokyo 142, Japan Shinshu Univ, Sch Med, Dept Med Genet, Matsumoto, Nagano 3908621, JapanArai, Takashi论文数: 0 引用数: 0 h-index: 0机构: Saitama Childrens Med Ctr, Div Clin Lab, Saitama, Japan Shinshu Univ, Sch Med, Dept Med Genet, Matsumoto, Nagano 3908621, JapanOh-ishi, Tsutomu论文数: 0 引用数: 0 h-index: 0机构: Saitama Childrens Med Ctr, Div Clin Lab, Saitama, Japan Shinshu Univ, Sch Med, Dept Med Genet, Matsumoto, Nagano 3908621, JapanKawame, Hiroshi论文数: 0 引用数: 0 h-index: 0机构: Ochanomizu Univ, Grad Sch Humanities & Sci, Dept Genet Counseling, Tokyo 112, Japan Shinshu Univ, Sch Med, Dept Med Genet, Matsumoto, Nagano 3908621, JapanNarumi, Yoko论文数: 0 引用数: 0 h-index: 0机构: Shinshu Univ, Sch Med, Dept Med Genet, Matsumoto, Nagano 3908621, Japan Shinshu Univ, Sch Med, Dept Med Genet, Matsumoto, Nagano 3908621, JapanOhashi, Hirofumi论文数: 0 引用数: 0 h-index: 0机构: Saitama Childrens Med Ctr, Div Med Genet, Saitama, Japan Shinshu Univ, Sch Med, Dept Med Genet, Matsumoto, Nagano 3908621, JapanFukushima, Yoshimitsu论文数: 0 引用数: 0 h-index: 0机构: Shinshu Univ, Sch Med, Dept Med Genet, Matsumoto, Nagano 3908621, Japan Shinshu Univ, Sch Med, Dept Med Genet, Matsumoto, Nagano 3908621, Japan
- [6] Genotype-phenotype correlation in 21 patients with Wolf-Hirschhorn syndrome using high resolution array comparative genome hybridisation (CGH)JOURNAL OF MEDICAL GENETICS, 2008, 45 (02) : 71 - 80Maas, N. M. C.论文数: 0 引用数: 0 h-index: 0机构: Catholic Univ Louvain, Univ Hosp, Ctr Human Genet, Louvain, Belgium Catholic Univ Louvain, Univ Hosp, Ctr Human Genet, Louvain, BelgiumVan Buggenhout, G.论文数: 0 引用数: 0 h-index: 0机构: Catholic Univ Louvain, Univ Hosp, Ctr Human Genet, Louvain, Belgium Catholic Univ Louvain, Univ Hosp, Ctr Human Genet, Louvain, BelgiumHannes, F.论文数: 0 引用数: 0 h-index: 0机构: Catholic Univ Louvain, Univ Hosp, Ctr Human Genet, Louvain, Belgium Catholic Univ Louvain, Univ Hosp, Ctr Human Genet, Louvain, BelgiumThienpont, B.论文数: 0 引用数: 0 h-index: 0机构: Catholic Univ Louvain, Univ Hosp, Ctr Human Genet, Louvain, Belgium Catholic Univ Louvain, Univ Hosp, Ctr Human Genet, Louvain, BelgiumSanlaville, D.论文数: 0 引用数: 0 h-index: 0机构: Hop Necker Enfants Malad, Assistance Publ Hop Paris, Dept Genet, Paris, France Catholic Univ Louvain, Univ Hosp, Ctr Human Genet, Louvain, BelgiumKok, K.论文数: 0 引用数: 0 h-index: 0机构: Univ Groningen, Univ Med Ctr Groningen, Dept Med Genet, Groningen, Netherlands Catholic Univ Louvain, Univ Hosp, Ctr Human Genet, Louvain, BelgiumMidro, A.论文数: 0 引用数: 0 h-index: 0机构: Med Univ Bialystok, Dept Clin Genet, Bialystok, Poland Catholic Univ Louvain, Univ Hosp, Ctr Human Genet, Louvain, BelgiumAndrieux, J.论文数: 0 引用数: 0 h-index: 0机构: St Vincent Hosp, Lille, France Catholic Univ Louvain, Univ Hosp, Ctr Human Genet, Louvain, BelgiumAnderlid, B-M论文数: 0 引用数: 0 h-index: 0机构: Karolinska Hosp, Dept Mol Med, Stockholm, Sweden Catholic Univ Louvain, Univ Hosp, Ctr Human Genet, Louvain, BelgiumSchoumans, J.论文数: 0 引用数: 0 h-index: 0机构: Karolinska Hosp, Dept Mol Med, Stockholm, Sweden Catholic Univ Louvain, Univ Hosp, Ctr Human Genet, Louvain, BelgiumHordijk, R.论文数: 0 引用数: 0 h-index: 0机构: Univ Groningen, Univ Med Ctr Groningen, Dept Med Genet, Groningen, Netherlands Catholic Univ Louvain, Univ Hosp, Ctr Human Genet, Louvain, BelgiumDevriendt, K.论文数: 0 引用数: 0 h-index: 0机构: Catholic Univ Louvain, Univ Hosp, Ctr Human Genet, Louvain, Belgium Catholic Univ Louvain, Univ Hosp, Ctr Human Genet, Louvain, BelgiumFryns, J-P论文数: 0 引用数: 0 h-index: 0机构: Catholic Univ Louvain, Univ Hosp, Ctr Human Genet, Louvain, Belgium Catholic Univ Louvain, Univ Hosp, Ctr Human Genet, Louvain, BelgiumVermeesch, J. R.论文数: 0 引用数: 0 h-index: 0机构: Catholic Univ Louvain, Univ Hosp, Ctr Human Genet, Louvain, Belgium Catholic Univ Louvain, Univ Hosp, Ctr Human Genet, Louvain, Belgium
- [7] Fine-grained facial phenotype-genotype analysis in Wolf-Hirschhorn syndromeEUROPEAN JOURNAL OF HUMAN GENETICS, 2012, 20 (01) : 33 - 40Hammond, Peter论文数: 0 引用数: 0 h-index: 0机构: UCL Inst Child Hlth, Mol Med Unit, London WC1N 1EH, England UCL Inst Child Hlth, Mol Med Unit, London WC1N 1EH, EnglandHannes, Femke论文数: 0 引用数: 0 h-index: 0机构: Univ Leuven, Ctr Human Genet, Louvain, Belgium UCL Inst Child Hlth, Mol Med Unit, London WC1N 1EH, EnglandSuttie, Michael论文数: 0 引用数: 0 h-index: 0机构: UCL Inst Child Hlth, Mol Med Unit, London WC1N 1EH, England UCL Inst Child Hlth, Mol Med Unit, London WC1N 1EH, EnglandDevriendt, Koen论文数: 0 引用数: 0 h-index: 0机构: Univ Leuven, Ctr Human Genet, Louvain, Belgium UCL Inst Child Hlth, Mol Med Unit, London WC1N 1EH, EnglandVermeesch, Joris Robert论文数: 0 引用数: 0 h-index: 0机构: Univ Leuven, Ctr Human Genet, Louvain, Belgium UCL Inst Child Hlth, Mol Med Unit, London WC1N 1EH, EnglandFaravelli, Francesca论文数: 0 引用数: 0 h-index: 0机构: EO Ospedali Galliera, SC Genet Umana, Genoa, Italy UCL Inst Child Hlth, Mol Med Unit, London WC1N 1EH, EnglandForzano, Francesca论文数: 0 引用数: 0 h-index: 0机构: EO Ospedali Galliera, SC Genet Umana, Genoa, Italy UCL Inst Child Hlth, Mol Med Unit, London WC1N 1EH, EnglandParekh, Susan论文数: 0 引用数: 0 h-index: 0机构: UCL Eastman Dent Inst, London, England UCL Inst Child Hlth, Mol Med Unit, London WC1N 1EH, EnglandWilliams, Steve论文数: 0 引用数: 0 h-index: 0机构: Sheffield Childrens Hosp, Dept Clin Genet, Sheffield, S Yorkshire, England UCL Inst Child Hlth, Mol Med Unit, London WC1N 1EH, EnglandMcMullan, Dominic论文数: 0 引用数: 0 h-index: 0机构: Birmingham Womens Hosp, Dept Cytogenet, Birmingham, W Midlands, England UCL Inst Child Hlth, Mol Med Unit, London WC1N 1EH, EnglandSouth, Sarah T.论文数: 0 引用数: 0 h-index: 0机构: Univ Utah, Dept Pediat, Div Med Genet, Salt Lake City, UT USA UCL Inst Child Hlth, Mol Med Unit, London WC1N 1EH, EnglandCarey, John C.论文数: 0 引用数: 0 h-index: 0机构: Univ Utah, Dept Pediat, Div Med Genet, Salt Lake City, UT USA UCL Inst Child Hlth, Mol Med Unit, London WC1N 1EH, EnglandQuarrell, Oliver论文数: 0 引用数: 0 h-index: 0机构: Sheffield Childrens Hosp, Dept Clin Genet, Sheffield, S Yorkshire, England UCL Inst Child Hlth, Mol Med Unit, London WC1N 1EH, England
- [8] Mapping the Wolf-Hirschhorn syndrome phenotype outside the currently defined Wolf-Hirschhorn syndrome critical region.AMERICAN JOURNAL OF HUMAN GENETICS, 2002, 71 (04) : 291 - 291Zollino, M论文数: 0 引用数: 0 h-index: 0机构: Univ Catt Sacro Curore, Inst Med Genet, Rome, ItalyLecce, R论文数: 0 引用数: 0 h-index: 0机构: Univ Catt Sacro Curore, Inst Med Genet, Rome, ItalyFischetto, R论文数: 0 引用数: 0 h-index: 0机构: Univ Catt Sacro Curore, Inst Med Genet, Rome, ItalySelicorni, A论文数: 0 引用数: 0 h-index: 0机构: Univ Catt Sacro Curore, Inst Med Genet, Rome, ItalyFaravelli, F论文数: 0 引用数: 0 h-index: 0机构: Univ Catt Sacro Curore, Inst Med Genet, Rome, ItalyMurdolo, M论文数: 0 引用数: 0 h-index: 0机构: Univ Catt Sacro Curore, Inst Med Genet, Rome, ItalyButt, C论文数: 0 引用数: 0 h-index: 0机构: Univ Catt Sacro Curore, Inst Med Genet, Rome, ItalyCapovilla, G论文数: 0 引用数: 0 h-index: 0机构: Univ Catt Sacro Curore, Inst Med Genet, Rome, ItalyMemo, L论文数: 0 引用数: 0 h-index: 0机构: Univ Catt Sacro Curore, Inst Med Genet, Rome, ItalyNeri, G论文数: 0 引用数: 0 h-index: 0机构: Univ Catt Sacro Curore, Inst Med Genet, Rome, Italy
- [9] Physical phenotype analysis in 16 Polish children with Wolf-Hirschhorn syndromeCHROMOSOME RESEARCH, 2005, 13 : 23 - 24Iwanowski, P. S.论文数: 0 引用数: 0 h-index: 0机构: Med Univ, Dept Clin Genet, Bialystok, Poland Med Univ, Dept Clin Genet, Bialystok, PolandPanasiuk, B.论文数: 0 引用数: 0 h-index: 0机构: Med Univ, Dept Clin Genet, Bialystok, Poland Med Univ, Dept Clin Genet, Bialystok, PolandZajczek, S.论文数: 0 引用数: 0 h-index: 0机构: Hereditary Canc Ctr, Dept Genet & Pathol, Szczecin, Poland Med Univ, Dept Clin Genet, Bialystok, PolandPilch, J.论文数: 0 引用数: 0 h-index: 0机构: Pediat Clin, Dept Neurol 2, Katowice, Poland Med Univ, Dept Clin Genet, Bialystok, PolandPiotrowicz, M.论文数: 0 引用数: 0 h-index: 0机构: Med Univ, Dept Med Genet, Aodz, Poland Med Univ, Dept Clin Genet, Bialystok, PolandWolnik-Brzozowska, D.论文数: 0 引用数: 0 h-index: 0机构: Med Univ, Dept Med Genet, Pozna D, Poland Med Univ, Dept Clin Genet, Bialystok, PolandKorniszewski, L.论文数: 0 引用数: 0 h-index: 0机构: Med Univ, Dept Pediat, Sect Diabetol & Birth Defects, Warsaw, Poland Med Univ, Dept Clin Genet, Bialystok, PolandMidro, A. T.论文数: 0 引用数: 0 h-index: 0机构: Med Univ, Dept Clin Genet, Bialystok, Poland Med Univ, Dept Clin Genet, Bialystok, Poland
- [10] Behavioural phenotype in two cases of Wolf-Hirschhorn syndromeEUROPEAN JOURNAL OF HUMAN GENETICS, 2002, 10 : 317 - 317Iwanowski, PS论文数: 0 引用数: 0 h-index: 0机构: Med Acad Bialystok, Dept Clin Genet, Bialystok, PolandStengel-Rutkowski, S论文数: 0 引用数: 0 h-index: 0机构: Med Acad Bialystok, Dept Clin Genet, Bialystok, PolandAnderlik, L论文数: 0 引用数: 0 h-index: 0机构: Med Acad Bialystok, Dept Clin Genet, Bialystok, PolandPilch, J论文数: 0 引用数: 0 h-index: 0机构: Med Acad Bialystok, Dept Clin Genet, Bialystok, PolandMidro, AT论文数: 0 引用数: 0 h-index: 0机构: Med Acad Bialystok, Dept Clin Genet, Bialystok, Poland