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Clinical, biochemical, and neuropsychiatric evaluation of a patient with a contiguous gene syndrome due to a microdeletion Xp11.3 including the Norrie disease locus and monoamine oxidase (MAOA and MAOB) genes.
Collins FA, Murphy DL, Reiss AL, Sims KB, Lewis JG, Freund L, Karoum F, Zhu D, Maumenee IH, Antonarakis SE. Collins FA, et al. Among authors: zhu d. Am J Med Genet. 1992 Jan 1;42(1):127-34. doi: 10.1002/ajmg.1320420126. Am J Med Genet. 1992. PMID: 1308352
Molecular genetic analysis in autosomal dominant keratoconus.
Rabinowitz YS, Maumenee IH, Lundergan MK, Puffenberger E, Zhu D, Antonarakis S, Francomano CA. Rabinowitz YS, et al. Among authors: zhu d. Cornea. 1992 Jul;11(4):302-8. doi: 10.1097/00003226-199207000-00005. Cornea. 1992. PMID: 1358551
Mutational analysis and clinical correlation in Leber congenital amaurosis.
Dharmaraj SR, Silva ER, Pina AL, Li YY, Yang JM, Carter CR, Loyer MK, El-Hilali HK, Traboulsi EK, Sundin OK, Zhu DK, Koenekoop RK, Maumenee IH. Dharmaraj SR, et al. Among authors: zhu dk. Ophthalmic Genet. 2000 Sep;21(3):135-50. Ophthalmic Genet. 2000. PMID: 11035546
A novel locus for Leber congenital amaurosis maps to chromosome 6q.
Dharmaraj S, Li Y, Robitaille JM, Silva E, Zhu D, Mitchell TN, Maltby LP, Baffoe-Bonnie AB, Maumenee IH. Dharmaraj S, et al. Among authors: zhu d. Am J Hum Genet. 2000 Jan;66(1):319-26. doi: 10.1086/302719. Am J Hum Genet. 2000. PMID: 10631161 Free PMC article. No abstract available.
Dominant inheritance of optic pits.
Stefko ST, Campochiaro P, Wang P, Li Y, Zhu D, Traboulsi EI. Stefko ST, et al. Among authors: zhu d. Am J Ophthalmol. 1997 Jul;124(1):112-3. doi: 10.1016/s0002-9394(14)71656-3. Am J Ophthalmol. 1997. PMID: 9222245
11,978 results
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