Mégarbané A - Search Results

1

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. 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

2

Trisomy for the distal segment of the short arm of chromosome 17 in a boy with mild mental retardation and some dysmorphic features.

Mégarbané A, Souraty N, Theophile D, Vekemans M, Samaras L, Ghorayeb Z. Mégarbané A, et al. Ann Genet. 1997;40(1):55-9. Ann Genet. 1997. PMID: 9150851

3

Brachytelephalangy with mental retardation, peculiar face and short stature in two sibs. A new MCA/MR syndrome?

Mégarbané A, Abi Moussa M. Mégarbané A, et al. Genet Couns. 1997;8(2):127-32. Genet Couns. 1997. PMID: 9219011

4

Ptosis, down-slanting palpebral fissures, hypertelorism, seizures and mental retardation: a possible new MCA/MR syndrome.

Mégarbané A, Le Merrer M, el Kallab K. Mégarbané A, et al. Clin Dysmorphol. 1997 Jul;6(3):239-44. doi: 10.1097/00019605-199707000-00007. Clin Dysmorphol. 1997. PMID: 9220194

5

Interstitial duplication of the short arm of chromosome 2: report of a new case and review.

Mégarbané A, Souraty N, Prieur M, Theophile D, Chédid P, Augé J, Vekemans M. Mégarbané A, et al. J Med Genet. 1997 Sep;34(9):783-6. doi: 10.1136/jmg.34.9.783. J Med Genet. 1997. PMID: 9321771 Free PMC article. Review.

6

Congenital glaucoma, limb deformities, skeletal dysplasia, and facial anomalies: report of another family.

Mégarbané A, Tomey K, Wakim G. Mégarbané A, et al. Am J Med Genet. 1997 Nov 28;73(1):67-71. doi: 10.1002/(sici)1096-8628(19971128)73:1<67::aid-ajmg13>3.0.co;2-p. Am J Med Genet. 1997. PMID: 9375925

7

New form of hidrotic ectodermal dysplasia in a Lebanese family.

Mégarbané A, Noujeim Z, Fabre M, Der Kaloustian VM. Mégarbané A, et al. Am J Med Genet. 1998 Jan 13;75(2):196-9. Am J Med Genet. 1998. PMID: 9450885

8

Craniosynostosis and marfanoid habitus without mental retardation: report of a third case.

Mégarbané A, Hokayem N. Mégarbané A, et al. Am J Med Genet. 1998 May 1;77(2):170-1. Am J Med Genet. 1998. PMID: 9605294 No abstract available.

9

Four sibs with dislocated elbows, bowed tibiae, scoliosis, deafness, cataract, microcephaly, and mental retardation: a new MCA/MR syndrome.

Mégarbané A, Kharrat K, Kreichati G. Mégarbané A, et al. J Med Genet. 1998 Sep;35(9):755-8. doi: 10.1136/jmg.35.9.755. J Med Genet. 1998. PMID: 9733034 Free PMC article.

10

The Usher syndrome in the Lebanese population and further refinement of the USH2A candidate region.

Saouda M, Mansour A, Bou Moglabey Y, El Zir E, Mustapha M, Chaib H, Nehmé A, Mégarbané A, Loiselet J, Petit C, Slim R. Saouda M, et al. Among authors: megarbane a. Hum Genet. 1998 Aug;103(2):193-8. doi: 10.1007/s004390050806. Hum Genet. 1998. PMID: 9760205

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