Moglabey YB - Search Results

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Microcephaly, cutis verticis gyrata of the scalp, retinitis pigmentosa, cataracts, sensorineural deafness, and mental retardation in two brothers.

Mégarbané A, Waked N, Chouery E, Moglabey YB, Saliba N, Mornet E, Serre JL, Slim R. Mégarbané A, et al. Among authors: moglabey yb. Am J Med Genet. 2001 Jan 22;98(3):244-9. doi: 10.1002/1096-8628(20010122)98:3<244::aid-ajmg1084>3.0.co;2-w. Am J Med Genet. 2001. PMID: 11169562

Further refinement of Pendred syndrome locus by homozygosity analysis to a 0.8 cM interval flanked by D7S496 and D7S2425.

Mustapha M, Azar ST, Moglabey YB, Saouda M, Zeitoun G, Loiselet J, Slim R. Mustapha M, et al. Among authors: moglabey yb. J Med Genet. 1998 Mar;35(3):202-4. doi: 10.1136/jmg.35.3.202. J Med Genet. 1998. PMID: 9541103 Free PMC article.

Genetic mapping of a maternal locus responsible for familial hydatidiform moles.

Moglabey YB, Kircheisen R, Seoud M, El Mogharbel N, Van den Veyver I, Slim R. Moglabey YB, et al. Hum Mol Genet. 1999 Apr;8(4):667-71. doi: 10.1093/hmg/8.4.667. Hum Mol Genet. 1999. PMID: 10072436

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