Teebi AS - Search Results

1

Newly recognized autosomal recessive acrofacial dysostosis syndrome resembling Nager syndrome.

Kennedy SJ, Teebi AS. Kennedy SJ, et al. Among authors: teebi as. Am J Med Genet A. 2004 Aug 15;129A(1):73-6. doi: 10.1002/ajmg.a.30113. Am J Med Genet A. 2004. PMID: 15266620

2

A novel missense mutation in the galactosyltransferase-I (B4GALT7) gene in a family exhibiting facioskeletal anomalies and Ehlers-Danlos syndrome resembling the progeroid type.

Faiyaz-Ul-Haque M, Zaidi SH, Al-Ali M, Al-Mureikhi MS, Kennedy S, Al-Thani G, Tsui LC, Teebi AS. Faiyaz-Ul-Haque M, et al. Among authors: teebi as. Am J Med Genet A. 2004 Jul 1;128A(1):39-45. doi: 10.1002/ajmg.a.30005. Am J Med Genet A. 2004. PMID: 15211654

3

Severe and mild phenotypes in Pfeiffer syndrome with splice acceptor mutations in exon IIIc of FGFR2.

Teebi AS, Kennedy S, Chun K, Ray PN. Teebi AS, et al. Am J Med Genet. 2002 Jan 1;107(1):43-7. doi: 10.1002/ajmg.10125. Am J Med Genet. 2002. PMID: 11807866

4

Clinical and genetic aspects of trigonocephaly: a study of 25 cases.

Azimi C, Kennedy SJ, Chitayat D, Chakraborty P, Clarke JT, Forrest C, Teebi AS. Azimi C, et al. Among authors: teebi as. Am J Med Genet A. 2003 Mar 1;117A(2):127-35. doi: 10.1002/ajmg.a.10021. Am J Med Genet A. 2003. PMID: 12567409

5

Microcephaly-cardiomyopathy syndrome: confirmation of the phenotype.

Kennedy SJ, Lee KJ, McCrindle BW, Teebi AS. Kennedy SJ, et al. Among authors: teebi as. J Med Genet. 1999 Nov;36(11):854-5. J Med Genet. 1999. PMID: 10544231 Free PMC article.

6

Detecting rearrangements in children using subtelomeric FISH and SKY.

Clarkson B, Pavenski K, Dupuis L, Kennedy S, Meyn S, Nezarati MM, Nie G, Weksberg R, Withers S, Quercia N, Teebi AS, Teshima I. Clarkson B, et al. Among authors: teebi as. Am J Med Genet. 2002 Feb 1;107(4):267-74. doi: 10.1002/ajmg.10240. Am J Med Genet. 2002. PMID: 11840482

7

Genetic analysis of patients with the Saethre-Chotzen phenotype.

Chun K, Teebi AS, Jung JH, Kennedy S, Laframboise R, Meschino WS, Nakabayashi K, Scherer SW, Ray PN, Teshima I. Chun K, et al. Among authors: teebi as. Am J Med Genet. 2002 Jun 15;110(2):136-43. doi: 10.1002/ajmg.10400. Am J Med Genet. 2002. PMID: 12116251

8

Novel mutation in the gene encoding c-Abl-binding protein SH3BP2 causes cherubism.

Lo B, Faiyaz-Ul-Haque M, Kennedy S, Aviv R, Tsui LC, Teebi AS. Lo B, et al. Among authors: teebi as. Am J Med Genet A. 2003 Aug 15;121A(1):37-40. doi: 10.1002/ajmg.a.20226. Am J Med Genet A. 2003. PMID: 12900899

9

Congenital mydriasis, patent ductus arteriosus, and congenital cystic lung disease: new syndromic spectrum?

Lemire BD, Buncic JR, Kennedy SJ, Dyack SJ, Teebi AS. Lemire BD, et al. Among authors: teebi as. Am J Med Genet A. 2004 Dec 15;131(3):318-9. doi: 10.1002/ajmg.a.30341. Am J Med Genet A. 2004. PMID: 15472996 No abstract available.

10

Craniofacial anomalies, cataracts, congenital heart disease, sacral neural tube defects, and growth and developmental retardation in two sisters: a new autosomal recessive MCA/MR syndrome?

Siegel-Bartlet J, Levin A, Teebi AS, Kennedy SJ. Siegel-Bartlet J, et al. Among authors: teebi as. J Med Genet. 2002 Feb;39(2):145-8. doi: 10.1136/jmg.39.2.145. J Med Genet. 2002. PMID: 11836368 Free PMC article. No abstract available.

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

176 results

Search Page

Filters