Mégarbané A - Search Results

1

Mapping of a new locus for autosomal recessive demyelinating Charcot-Marie-Tooth disease to 19q13.1-13.3 in a large consanguineous Lebanese family: exclusion of MAG as a candidate gene.

Delague V, Bareil C, Tuffery S, Bouvagnet P, Chouery E, Koussa S, Maisonobe T, Loiselet J, Mégarbané A, Claustres M. Delague V, et al. Among authors: megarbane a. Am J Hum Genet. 2000 Jul;67(1):236-43. doi: 10.1086/302980. Epub 2000 Jun 2. Am J Hum Genet. 2000. PMID: 10848494 Free PMC article.

2

Clinical manifestation of a severe neonatal progeroid syndrome.

Mégarbané A, Loiselet J. Mégarbané A, et al. Clin Genet. 1997 Mar;51(3):200-4. doi: 10.1111/j.1399-0004.1997.tb02453.x. Clin Genet. 1997. PMID: 9137887

3

Cystic fibrosis in Lebanon: distribution of CFTR mutations among Arab communities.

Desgeorges M, Mégarbané A, Guittard C, Carles S, Loiselet J, Demaille J, Claustres M. Desgeorges M, et al. Among authors: megarbane a. Hum Genet. 1997 Aug;100(2):279-83. doi: 10.1007/s004390050505. Hum Genet. 1997. PMID: 9254864

4

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

5

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

6

Autosomal dominant secundum atrial septal defect with various cardiac and noncardiac defects: a new midline disorder.

Mégarbané A, Stephan E, Kassab R, Ashoush R, Salem N, Bouvagnet P, Loiselet J. Mégarbané A, et al. Am J Med Genet. 1999 Mar 19;83(3):193-200. doi: 10.1002/(sici)1096-8628(19990319)83:3<193::aid-ajmg10>3.0.co;2-m. Am J Med Genet. 1999. PMID: 10096596

7

Microcephaly, colobomatous microphthalmia, short stature, and severe psychomotor retardation in two male cousins: a new MCA/MR syndrome?

Mégarbané A, Haddad-Zebouni S, Nabbout R, Khoury AH, Traboulsi EI. Mégarbané A, et al. Am J Med Genet. 1999 Mar 12;83(2):82-7. Am J Med Genet. 1999. PMID: 10190477

8

Autosomal recessive congenital cerebellar hypoplasia and short stature in a large inbred family.

Mégarbané A, Delague V, Salem N, Loiselet J. Mégarbané A, et al. Am J Med Genet. 1999 Nov 5;87(1):88-90. Am J Med Genet. 1999. PMID: 10528257 No abstract available.

9

Two sibs with myoclonic epilepsy, congenital deafness, macular dystrophy, and psychiatric disorders.

Mégarbané A, Khalil G, Waked N, Rötig A, Caillaud C, Loiselet J. Mégarbané A, et al. Am J Med Genet. 1999 Dec 3;87(4):289-93. doi: 10.1002/(sici)1096-8628(19991203)87:4<289::aid-ajmg1>3.0.co;2-t. Am J Med Genet. 1999. PMID: 10588831

10

Exclusion of chromosome 9 helps to identify mild variants of acromesomelic dysplasia Maroteaux type.

Faivre L, Le Merrer M, Megarbane A, Gilbert B, Mortier G, Cusin V, Munnich A, Maroteaux P, Cormier-Daire V. Faivre L, et al. Among authors: megarbane a. J Med Genet. 2000 Jan;37(1):52-4. doi: 10.1136/jmg.37.1.52. J Med Genet. 2000. PMID: 10633136 Free PMC article.

Save citations to file

Email citations

Send citations to clipboard

Add to Collections

Add to My Bibliography

Create a file for external citation management software

Your saved search

Your RSS Feed

My Custom Filters

Publication date

Text availability

Article attribute

Article type

Article Language

Species

Sex

Age

Other

397 results

Search Page

Filters