共 50 条
- [1] Rare Causes of Osteogenesis Imperfecta are Common in Consanguineous PedigreesHORMONE RESEARCH IN PAEDIATRICS, 2019, 91 : 214 - 214Kaygusuz, Sare Betul论文数: 0 引用数: 0 h-index: 0机构: Marmara Univ, Fac Med, Dept Pediat Endocrinol, Istanbul, Turkey Marmara Univ, Fac Med, Dept Pediat Endocrinol, Istanbul, TurkeyArman, Ahmet论文数: 0 引用数: 0 h-index: 0机构: Marmara Univ, Fac Med, Dept Med Genet, Istanbul, Turkey Marmara Univ, Fac Med, Dept Pediat Endocrinol, Istanbul, TurkeyAbali, Saygin论文数: 0 引用数: 0 h-index: 0机构: Acibadem Univ, Fac Med, Dept Pediat Endocrinol, Istanbul, Turkey Marmara Univ, Fac Med, Dept Pediat Endocrinol, Istanbul, TurkeyAta, Pinar论文数: 0 引用数: 0 h-index: 0机构: Marmara Univ, Fac Med, Dept Med Genet, Istanbul, Turkey Marmara Univ, Fac Med, Dept Pediat Endocrinol, Istanbul, Turkey论文数: 引用数: h-index:机构:Eltan, Mehmet论文数: 0 引用数: 0 h-index: 0机构: Marmara Univ, Fac Med, Dept Pediat Endocrinol, Istanbul, Turkey Marmara Univ, Fac Med, Dept Pediat Endocrinol, Istanbul, TurkeyAbali, Zehra Yavas论文数: 0 引用数: 0 h-index: 0机构: Marmara Univ, Fac Med, Dept Pediat Endocrinol, Istanbul, Turkey Marmara Univ, Fac Med, Dept Pediat Endocrinol, Istanbul, TurkeyHelvacioglu, Didem论文数: 0 引用数: 0 h-index: 0机构: Marmara Univ, Fac Med, Dept Pediat Endocrinol, Istanbul, Turkey Marmara Univ, Fac Med, Dept Pediat Endocrinol, Istanbul, TurkeyTosun, Busra Gurpinar论文数: 0 引用数: 0 h-index: 0机构: Marmara Univ, Fac Med, Dept Pediat Endocrinol, Istanbul, Turkey Marmara Univ, Fac Med, Dept Pediat Endocrinol, Istanbul, TurkeyMenevse, Tuba Seven论文数: 0 引用数: 0 h-index: 0机构: Marmara Univ, Fac Med, Dept Pediat Endocrinol, Istanbul, Turkey Marmara Univ, Fac Med, Dept Pediat Endocrinol, Istanbul, TurkeyGuran, Tulay论文数: 0 引用数: 0 h-index: 0机构: Marmara Univ, Fac Med, Dept Pediat Endocrinol, Istanbul, Turkey Marmara Univ, Fac Med, Dept Pediat Endocrinol, Istanbul, TurkeyBereket, Abdullah论文数: 0 引用数: 0 h-index: 0机构: Marmara Univ, Fac Med, Dept Pediat Endocrinol, Istanbul, Turkey Marmara Univ, Fac Med, Dept Pediat Endocrinol, Istanbul, TurkeyTuran, Serap论文数: 0 引用数: 0 h-index: 0机构: Marmara Univ, Fac Med, Dept Pediat Endocrinol, Istanbul, Turkey Marmara Univ, Fac Med, Dept Pediat Endocrinol, Istanbul, Turkey
- [2] WHOLE EXOME SEQUENCING OF AFFECTED INDIVIDUALS FROM LARGE CONSANGUINEOUS PEDIGREES WITH PSYCHOTIC/AFFECTIVE DISORDERS FROM PAKISTANEUROPEAN NEUROPSYCHOPHARMACOLOGY, 2017, 27 : S399 - S400He, Qin论文数: 0 引用数: 0 h-index: 0机构: Univ Montreal, Montreal, PQ, Canada Univ Montreal, Montreal, PQ, CanadaHajji, Ilyass论文数: 0 引用数: 0 h-index: 0机构: Univ Montreal, Inst Univ Sante Mentale Montreal, Ctr Rech, Montreal, PQ, Canada Univ Montreal, Montreal, PQ, CanadaJimenez, Daniel论文数: 0 引用数: 0 h-index: 0机构: Univ Montreal, Inst Univ Sante Mentale Montreal, Ctr Rech, Montreal, PQ, Canada Univ Montreal, Montreal, PQ, CanadaBenbetka, Souhila论文数: 0 引用数: 0 h-index: 0机构: Univ Montreal, Inst Univ Sante Mentale Montreal, Ctr Rech, Montreal, PQ, Canada Univ Montreal, Montreal, PQ, CanadaJohnson, Amelie论文数: 0 引用数: 0 h-index: 0机构: Univ Montreal, Inst Univ Sante Mentale Montreal, Ctr Rech, Montreal, PQ, Canada Univ Montreal, Montreal, PQ, CanadaDionne-Laporte, Alexandre论文数: 0 引用数: 0 h-index: 0机构: McGill Univ, Montreal Neurol Inst & Hosp, Montreal, PQ, Canada Univ Montreal, Montreal, PQ, CanadaSpiegelman, Dan论文数: 0 引用数: 0 h-index: 0机构: McGill Univ, Montreal Neurol Inst & Hosp, Montreal, PQ, Canada Univ Montreal, Montreal, PQ, CanadaJoober, Ridha论文数: 0 引用数: 0 h-index: 0机构: McGill Univ, Douglas Mental Hlth Univ Inst, Montreal, PQ, Canada Univ Montreal, Montreal, PQ, CanadaDube, Marie-Pierre论文数: 0 引用数: 0 h-index: 0机构: Montreal Heart Inst, Stat Genet Res Grp, Montreal, PQ, Canada Univ Montreal, Montreal, PQ, CanadaDeLisi, Lynn论文数: 0 引用数: 0 h-index: 0机构: VA Boston Healthcare, Boston, MA USA Univ Montreal, Montreal, PQ, CanadaRouleau, Guy A.论文数: 0 引用数: 0 h-index: 0机构: McGill Univ, Montreal Neurol Inst & Hosp, Montreal, PQ, Canada Univ Montreal, Montreal, PQ, CanadaXiong, Lan论文数: 0 引用数: 0 h-index: 0机构: Inst Univ Sante Mentale Montreal, Ctr Rech, Montreal, PQ, Canada Univ Montreal, Dept Psychiat, Montreal, PQ, Canada Univ Montreal, Montreal, PQ, Canada
- [3] Identification of causative mutations in consanguineous pedigrees from Pakistan with recessive retinal degeneration by whole exome analysisINVESTIGATIVE OPHTHALMOLOGY & VISUAL SCIENCE, 2013, 54 (15)Biswas, Pooja论文数: 0 引用数: 0 h-index: 0机构: Univ Calif San Diego, Shiley Eye Ctr, San Diego, CA 92103 USA Univ Calif San Diego, Shiley Eye Ctr, San Diego, CA 92103 USAMaranhao, Bruno论文数: 0 引用数: 0 h-index: 0机构: Univ Calif San Diego, Shiley Eye Ctr, San Diego, CA 92103 USA Univ Calif San Diego, Bioengn, San Diego, CA 92103 USA Univ Calif San Diego, Shiley Eye Ctr, San Diego, CA 92103 USALee, Pauline论文数: 0 引用数: 0 h-index: 0机构: Univ Calif San Diego, Shiley Eye Ctr, San Diego, CA 92103 USA Univ Calif San Diego, Shiley Eye Ctr, San Diego, CA 92103 USASuk, John论文数: 0 引用数: 0 h-index: 0机构: Univ Calif San Diego, Shiley Eye Ctr, San Diego, CA 92103 USA Univ Calif San Diego, Shiley Eye Ctr, San Diego, CA 92103 USANavani, Mili论文数: 0 引用数: 0 h-index: 0机构: Univ Calif San Diego, Shiley Eye Ctr, San Diego, CA 92103 USA Univ Calif San Diego, Shiley Eye Ctr, San Diego, CA 92103 USAKhan, Shahid论文数: 0 引用数: 0 h-index: 0机构: Johns Hopkins Univ, Sch Med, Wilmer Eye Inst, Baltimore, MD 21205 USA Univ Calif San Diego, Shiley Eye Ctr, San Diego, CA 92103 USAButt, Nadeem论文数: 0 引用数: 0 h-index: 0机构: Univ Hlth Sci, Allama Iqbal Med Coll, Lahore, Pakistan Univ Calif San Diego, Shiley Eye Ctr, San Diego, CA 92103 USARiazuddin, Sheikh论文数: 0 引用数: 0 h-index: 0机构: Univ Hlth Sci, Allama Iqbal Med Coll, Lahore, Pakistan Univ Punjab Lahore, Natl Ctr Excellence Mol Biol, Lahore, Pakistan Univ Calif San Diego, Shiley Eye Ctr, San Diego, CA 92103 USARiazuddin, S. Amer论文数: 0 引用数: 0 h-index: 0机构: Johns Hopkins Univ, Sch Med, Wilmer Eye Inst, Baltimore, MD 21205 USA Univ Calif San Diego, Shiley Eye Ctr, San Diego, CA 92103 USAAyyagari, Radha论文数: 0 引用数: 0 h-index: 0机构: Univ Calif San Diego, Shiley Eye Ctr, San Diego, CA 92103 USA Univ Calif San Diego, Shiley Eye Ctr, San Diego, CA 92103 USA
- [4] genetic causes of syndromic and non-syndromic forms of monogenic obesity: a study in 37 consanguineous families from pakistanEUROPEAN JOURNAL OF HUMAN GENETICS, 2024, 32 : 419 - 420Pena, Elionora论文数: 0 引用数: 0 h-index: 0机构: Inovo Nordisk Fdn Ctr Basic Metab Res, Copenhagen, Denmark Inovo Nordisk Fdn Ctr Basic Metab Res, Copenhagen, DenmarkNiazi, Robina Khan论文数: 0 引用数: 0 h-index: 0机构: Int Islamic Univ, Islamabad, Pakistan Inovo Nordisk Fdn Ctr Basic Metab Res, Copenhagen, DenmarkUllah, Asmat论文数: 0 引用数: 0 h-index: 0机构: Inovo Nordisk Fdn Ctr Basic Metab Res, Copenhagen, Denmark Inovo Nordisk Fdn Ctr Basic Metab Res, Copenhagen, DenmarkThuesen, Anne Cathrine Baun论文数: 0 引用数: 0 h-index: 0机构: Inovo Nordisk Fdn Ctr Basic Metab Res, Copenhagen, Denmark Inovo Nordisk Fdn Ctr Basic Metab Res, Copenhagen, DenmarkSchubert, Mikkel论文数: 0 引用数: 0 h-index: 0机构: Inovo Nordisk Fdn Ctr Basic Metab Res, Copenhagen, Denmark Inovo Nordisk Fdn Ctr Basic Metab Res, Copenhagen, DenmarkGjesing, Anette Prior论文数: 0 引用数: 0 h-index: 0机构: Inovo Nordisk Fdn Ctr Basic Metab Res, Copenhagen, Denmark Inovo Nordisk Fdn Ctr Basic Metab Res, Copenhagen, DenmarkHansen, Torben论文数: 0 引用数: 0 h-index: 0机构: Inovo Nordisk Fdn Ctr Basic Metab Res, Copenhagen, Denmark Inovo Nordisk Fdn Ctr Basic Metab Res, Copenhagen, Denmark
- [5] Genetic causes of MCPH in consanguineous Pakistani familiesCLINICAL GENETICS, 2016, 89 (06) : 744 - 745Kraemer, Nadine论文数: 0 引用数: 0 h-index: 0机构: Univ Azad Jammu & Kashmir, Inst Cell Biol & Neurobiol, Muzaffarabad, Pakistan Univ Azad Jammu & Kashmir, Dept Pediat Neurol, Muzaffarabad, Pakistan Univ Azad Jammu & Kashmir, Inst Cell Biol & Neurobiol, Muzaffarabad, PakistanPicker-Minh, Sylvie论文数: 0 引用数: 0 h-index: 0机构: Univ Azad Jammu & Kashmir, Inst Cell Biol & Neurobiol, Muzaffarabad, Pakistan Univ Azad Jammu & Kashmir, Dept Pediat Neurol, Muzaffarabad, Pakistan Univ Azad Jammu & Kashmir, Inst Cell Biol & Neurobiol, Muzaffarabad, PakistanAbbasi, Ansar A.论文数: 0 引用数: 0 h-index: 0机构: Univ Azad Jammu & Kashmir, Dept Zool, Muzaffarabad, Pakistan MUST, Dept Zool, Mirpur, Pakistan Univ Azad Jammu & Kashmir, Inst Cell Biol & Neurobiol, Muzaffarabad, PakistanFroehler, Sebastian论文数: 0 引用数: 0 h-index: 0机构: Berlin Inst Hlth, Genom Core, Berlin, Germany Univ Azad Jammu & Kashmir, Inst Cell Biol & Neurobiol, Muzaffarabad, PakistanNinnemann, Olaf论文数: 0 引用数: 0 h-index: 0机构: Univ Azad Jammu & Kashmir, Inst Cell Biol & Neurobiol, Muzaffarabad, Pakistan Univ Azad Jammu & Kashmir, Inst Cell Biol & Neurobiol, Muzaffarabad, PakistanKhan, Muhammad N.论文数: 0 引用数: 0 h-index: 0机构: Univ Azad Jammu & Kashmir, Dept Biotechnol, Muzaffarabad, Pakistan Univ Azad Jammu & Kashmir, Inst Cell Biol & Neurobiol, Muzaffarabad, PakistanAli, Ghazanfar论文数: 0 引用数: 0 h-index: 0机构: Univ Azad Jammu & Kashmir, Dept Biotechnol, Muzaffarabad, Pakistan Univ Azad Jammu & Kashmir, Inst Cell Biol & Neurobiol, Muzaffarabad, PakistanChen, Wei论文数: 0 引用数: 0 h-index: 0机构: Berlin Inst Hlth, Genom Core, Berlin, Germany Univ Azad Jammu & Kashmir, Inst Cell Biol & Neurobiol, Muzaffarabad, PakistanKaindl, Angela M.论文数: 0 引用数: 0 h-index: 0机构: Univ Azad Jammu & Kashmir, Inst Cell Biol & Neurobiol, Muzaffarabad, Pakistan Univ Azad Jammu & Kashmir, Dept Pediat Neurol, Muzaffarabad, Pakistan Univ Azad Jammu & Kashmir, Sozialpadiatr Zentrum SPZ, Muzaffarabad, Pakistan Univ Azad Jammu & Kashmir, Inst Cell Biol & Neurobiol, Muzaffarabad, Pakistan
- [6] CONGENITAL HEART DISEASES, A CONSEQUENCE OF CONSANGUINEOUS MARRIAGES IN PUNJAB, PAKISTANPAKISTAN HEART JOURNAL, 2022, 55 (01): : 28 - 32Mughal, Abdul Razzaq论文数: 0 引用数: 0 h-index: 0机构: Faisalabad Inst Cardiol, Faisalabad, Pakistan Faisalabad Inst Cardiol, Faisalabad, PakistanHina, Saira论文数: 0 引用数: 0 h-index: 0机构: Govt Coll Women Univ, Faisalabad, Pakistan Faisalabad Inst Cardiol, Faisalabad, PakistanBashir, Ayesha论文数: 0 引用数: 0 h-index: 0机构: Govt Coll Women Univ, Faisalabad, Pakistan Faisalabad Inst Cardiol, Faisalabad, PakistanMughal, Safia论文数: 0 引用数: 0 h-index: 0机构: Social Secur Hosp, Faisalabad, Pakistan Faisalabad Inst Cardiol, Faisalabad, Pakistan
- [7] GENETIC HETEROGENEITY IN A CONSANGUINEOUS PEDIGREE WITH INTELLECTUAL DISABILITY AND AUTISTIC FEATURES FROM PAKISTANEUROPEAN NEUROPSYCHOPHARMACOLOGY, 2017, 27 : S322 - S322Johnson, Amelie Musa论文数: 0 引用数: 0 h-index: 0机构: Univ Montreal, Montreal, PQ, Canada Univ Montreal, Montreal, PQ, CanadaLi, Shu论文数: 0 引用数: 0 h-index: 0机构: Capital Med Univ, Beijing Tiantan Hosp, Dept Neurosurg, Beijing, Peoples R China Univ Montreal, Montreal, PQ, CanadaHe, Qin论文数: 0 引用数: 0 h-index: 0机构: Inst Univ Sante Ment Montreal, Ctr Rech, Montreal, PQ, Canada Univ Montreal, Montreal, PQ, CanadaLaurent, Sandra论文数: 0 引用数: 0 h-index: 0机构: McGill Univ, Montreal Neurol Inst & Hosp, Montreal, PQ, Canada Univ Montreal, Montreal, PQ, CanadaSpiegelman, Dan论文数: 0 引用数: 0 h-index: 0机构: McGill Univ, Montreal Neurol Inst & Hosp, Montreal, PQ, Canada Univ Montreal, Montreal, PQ, CanadaAppeltshauser, Luise论文数: 0 引用数: 0 h-index: 0机构: Univ Julius Maximilians Univ Wurzburg, Wurzburg, Germany Univ Montreal, Montreal, PQ, CanadaChristian, Mehtab论文数: 0 引用数: 0 h-index: 0机构: Inst Univ Sante Ment Montreal, Ctr Rech, Montreal, PQ, Canada Univ Montreal, Montreal, PQ, CanadaNanjian, Zohair论文数: 0 引用数: 0 h-index: 0机构: Ma Ayesha Mem Ctr, Karachi, Pakistan Univ Montreal, Montreal, PQ, CanadaBrohi, Muhammad Qasim论文数: 0 引用数: 0 h-index: 0机构: Sir Cowasji Jehangir Inst Psychiat, Hyderabad, Sindh, Pakistan Univ Montreal, Montreal, PQ, CanadaXiong, Lan论文数: 0 引用数: 0 h-index: 0机构: Inst Univ Sante Ment Montreal, Ctr Rech, Montreal, PQ, Canada Univ Montreal, Dept Psychiat, Montreal, PQ, Canada Univ Montreal, Montreal, PQ, Canada
- [8] Genetic anomalies in congenital cataractACTA OPHTHALMOLOGICA, 2017, 95Bremond-Gignac, D.论文数: 0 引用数: 0 h-index: 0机构: Hop Necker Enfants Malad, Serv Ophtalmol, Paris, France Hop Necker Enfants Malad, Serv Ophtalmol, Paris, Francedes Roziers, C. Burin论文数: 0 引用数: 0 h-index: 0机构: Inst Imagine, INSERM, U1163, Paris, France Hop Necker Enfants Malad, Serv Ophtalmol, Paris, FranceBeugnet, C.论文数: 0 引用数: 0 h-index: 0机构: Hop Necker Enfants Malad, Lab Genet Mol, Paris, France Hop Necker Enfants Malad, Serv Ophtalmol, Paris, FranceFourrage, C.论文数: 0 引用数: 0 h-index: 0机构: Hop Necker Enfants Malad, Lab Genet Mol, Paris, France Hop Necker Enfants Malad, Serv Ophtalmol, Paris, FranceMoriniere, V.论文数: 0 引用数: 0 h-index: 0机构: Hop Necker Enfants Malad, Lab Genet Mol, Paris, France Hop Necker Enfants Malad, Serv Ophtalmol, Paris, FranceRobert, M.论文数: 0 引用数: 0 h-index: 0机构: Hop Necker Enfants Malad, Serv Ophtalmol, Paris, France Hop Necker Enfants Malad, Serv Ophtalmol, Paris, FranceValleix, S.论文数: 0 引用数: 0 h-index: 0机构: Hop Necker Enfants Malad, Lab Genet Mol, Paris, France Hop Necker Enfants Malad, INSERM, U1163, Paris, France Inst Imagine, Paris, France Hop Necker Enfants Malad, Serv Ophtalmol, Paris, France
- [9] Genetic testing for congenital cataractINVESTIGATIVE OPHTHALMOLOGY & VISUAL SCIENCE, 2015, 56 (07)Weed, Matthew C.论文数: 0 引用数: 0 h-index: 0机构: Univ Iowa, Dept Ophthalmol, Carver Coll Med, Stephen A Wynn Inst Vis Res, Iowa City, IA 52242 USA Univ Iowa, Dept Ophthalmol, Carver Coll Med, Stephen A Wynn Inst Vis Res, Iowa City, IA 52242 USALambert, Scott R.论文数: 0 引用数: 0 h-index: 0机构: Emory Eye Ctr, Atlanta, GA USA Univ Iowa, Dept Ophthalmol, Carver Coll Med, Stephen A Wynn Inst Vis Res, Iowa City, IA 52242 USALarson, Scott A.论文数: 0 引用数: 0 h-index: 0机构: Univ Iowa, Dept Ophthalmol & Visual Sci, Iowa City, IA USA Univ Iowa, Dept Ophthalmol, Carver Coll Med, Stephen A Wynn Inst Vis Res, Iowa City, IA 52242 USAOlson, Richard J.论文数: 0 引用数: 0 h-index: 0机构: Univ Iowa, Dept Ophthalmol & Visual Sci, Iowa City, IA USA Univ Iowa, Dept Ophthalmol, Carver Coll Med, Stephen A Wynn Inst Vis Res, Iowa City, IA 52242 USALongmuir, Susannah Q.论文数: 0 引用数: 0 h-index: 0机构: Univ Iowa, Dept Ophthalmol & Visual Sci, Iowa City, IA USA Univ Iowa, Dept Ophthalmol, Carver Coll Med, Stephen A Wynn Inst Vis Res, Iowa City, IA 52242 USADeLuca, Adam P.论文数: 0 引用数: 0 h-index: 0机构: Univ Iowa, Dept Ophthalmol, Carver Coll Med, Stephen A Wynn Inst Vis Res, Iowa City, IA 52242 USA Univ Iowa, Dept Ophthalmol, Carver Coll Med, Stephen A Wynn Inst Vis Res, Iowa City, IA 52242 USAKennedy, Elizabeth L.论文数: 0 引用数: 0 h-index: 0机构: Univ Iowa, Dept Ophthalmol, Carver Coll Med, Stephen A Wynn Inst Vis Res, Iowa City, IA 52242 USA Univ Iowa, Dept Ophthalmol, Carver Coll Med, Stephen A Wynn Inst Vis Res, Iowa City, IA 52242 USAStone, Edwin M.论文数: 0 引用数: 0 h-index: 0机构: Univ Iowa, Dept Ophthalmol, Carver Coll Med, Stephen A Wynn Inst Vis Res, Iowa City, IA 52242 USA Univ Iowa, Dept Ophthalmol, Carver Coll Med, Stephen A Wynn Inst Vis Res, Iowa City, IA 52242 USADrack, Arlene V.论文数: 0 引用数: 0 h-index: 0机构: Univ Iowa, Dept Ophthalmol, Carver Coll Med, Stephen A Wynn Inst Vis Res, Iowa City, IA 52242 USA Univ Iowa, Dept Ophthalmol, Carver Coll Med, Stephen A Wynn Inst Vis Res, Iowa City, IA 52242 USA
- [10] A common ancestral mutation in CRYBB3 identified in multiple consanguineous pedigrees with congenital cataractsINVESTIGATIVE OPHTHALMOLOGY & VISUAL SCIENCE, 2015, 56 (07)Jiao, Xiaodong论文数: 0 引用数: 0 h-index: 0机构: NEI, Ophthalm Genet & Visual Funct Branch, NIH, Bethesda, MD 20892 USA NEI, Ophthalm Genet & Visual Funct Branch, NIH, Bethesda, MD 20892 USAKabir, Firoz论文数: 0 引用数: 0 h-index: 0机构: Johns Hopkins Univ, Sch Med, Wilmer Eye Inst, Baltimore, MD 21205 USA NEI, Ophthalm Genet & Visual Funct Branch, NIH, Bethesda, MD 20892 USAKhan, Arif论文数: 0 引用数: 0 h-index: 0机构: King Khalid Eye Specialist Hosp, Div Pediat Ophthalmol, Riyadh, Saudi Arabia NEI, Ophthalm Genet & Visual Funct Branch, NIH, Bethesda, MD 20892 USAWang, Qiwei论文数: 0 引用数: 0 h-index: 0机构: NEI, Ophthalm Genet & Visual Funct Branch, NIH, Bethesda, MD 20892 USA NEI, Ophthalm Genet & Visual Funct Branch, NIH, Bethesda, MD 20892 USALi, David论文数: 0 引用数: 0 h-index: 0机构: NEI, Ophthalm Genet & Visual Funct Branch, NIH, Bethesda, MD 20892 USA NEI, Ophthalm Genet & Visual Funct Branch, NIH, Bethesda, MD 20892 USAKhan, Shaheen N.论文数: 0 引用数: 0 h-index: 0机构: Univ Punjab, Natl Ctr Excellence Moloecular Biol, Lahore, Pakistan NEI, Ophthalm Genet & Visual Funct Branch, NIH, Bethesda, MD 20892 USAHusnain, Tayyab论文数: 0 引用数: 0 h-index: 0机构: Univ Punjab, Natl Ctr Excellence Moloecular Biol, Lahore, Pakistan NEI, Ophthalm Genet & Visual Funct Branch, NIH, Bethesda, MD 20892 USARiazuddin, Sheikh论文数: 0 引用数: 0 h-index: 0机构: Univ Punjab, Natl Ctr Excellence Moloecular Biol, Lahore, Pakistan Univ Hlth Sci, Allama Iqbal Med Coll, Lahore, Pakistan NEI, Ophthalm Genet & Visual Funct Branch, NIH, Bethesda, MD 20892 USAHejtmancik, J. Fielding论文数: 0 引用数: 0 h-index: 0机构: NEI, Ophthalm Genet & Visual Funct Branch, NIH, Bethesda, MD 20892 USA NEI, Ophthalm Genet & Visual Funct Branch, NIH, Bethesda, MD 20892 USARiazuddin, S. Amer论文数: 0 引用数: 0 h-index: 0机构: Johns Hopkins Univ, Sch Med, Wilmer Eye Inst, Baltimore, MD 21205 USA Univ Punjab, Natl Ctr Excellence Moloecular Biol, Lahore, Pakistan NEI, Ophthalm Genet & Visual Funct Branch, NIH, Bethesda, MD 20892 USA