Mégarbané A - Search Results

1

Craniofacial anomalies, deafness, brachydactyly, short stature, and moderate mental retardation due to a cryptic 6p;11q translocation.

Mégarbané A, Bejjani BA, Shaffer LG, Jambart S, Souraty N, Kashork CD, Le Merrer M. Mégarbané A, et al. Am J Med Genet. 2002 Feb 15;108(1):69-74. doi: 10.1002/ajmg.10222. Am J Med Genet. 2002. PMID: 11857553

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

Ophthalmo-acromelic syndrome (Waardenburg) with split hand and polydactyly.

Mégarbané A, Souraty N, Tamraz J. Mégarbané A, et al. Genet Couns. 1998;9(3):195-9. Genet Couns. 1998. PMID: 9777341

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