Teebi AS - Search Results

1

Azouz EM, Teebi AS, Eydoux P, Chen MF, Fassier F. Azouz EM, et al. Among authors: teebi as. Can Assoc Radiol J. 1998 Apr;49(2):105-9. Can Assoc Radiol J. 1998. PMID: 9561013 Review.

2

Bone dysplasia series. Achondroplasia, hypochondroplasia and thanatophoric dysplasia: review and update.

Lemyre E, Azouz EM, Teebi AS, Glanc P, Chen MF. Lemyre E, et al. Among authors: teebi as. Can Assoc Radiol J. 1999 Jun;50(3):185-97. Can Assoc Radiol J. 1999. PMID: 10405653 Review.

3

Arthrogryposis multiplex congenita, craniofacial, and ophthalmological abnormalities and normal intelligence: a new syndrome?

al-Ghamdi MA, Polomeno RC, Chitayat D, Azouz EM, Teebi AS. al-Ghamdi MA, et al. Among authors: teebi as. Am J Med Genet. 1997 Sep 5;71(4):401-5. doi: 10.1002/(sici)1096-8628(19970905)71:4<401::aid-ajmg6>3.0.co;2-w. Am J Med Genet. 1997. PMID: 9286445

4

Developmental anomalies suggestive of the human homologue of the mouse mutant disorganization.

Elliott AM, Chen MF, Azouz EM, Teebi AS. Elliott AM, et al. Among authors: teebi as. Am J Med Genet. 1995 Jan 16;55(2):240-3. doi: 10.1002/ajmg.1320550218. Am J Med Genet. 1995. PMID: 7717426

5

Keutel syndrome: further characterization and review.

Teebi AS, Lambert DM, Kaye GM, Al-Fifi S, Tewfik TL, Azouz EM. Teebi AS, et al. Am J Med Genet. 1998 Jun 30;78(2):182-7. Am J Med Genet. 1998. PMID: 9674914 Review.

6

Progressive erosive arthropathy with contractures, multicentric osteolysis-like changes, characteristic craniofacial appearance, and dermatological abnormalities: a new syndrome?

Teebi AS, Elliott AM, Azouz EM, Lachman RS. Teebi AS, et al. Am J Med Genet. 2001 May 1;100(3):198-203. doi: 10.1002/ajmg.1263. Am J Med Genet. 2001. PMID: 11343304

7

Spastic paraplegia, optic atrophy, microcephaly with normal intelligence, and XY sex reversal: a new autosomal recessive syndrome?

Teebi AS, Miller S, Ostrer H, Eydoux P, Colomb-Brockmann C, Oudjhane K, Watters G. Teebi AS, et al. J Med Genet. 1998 Sep;35(9):759-62. doi: 10.1136/jmg.35.9.759. J Med Genet. 1998. PMID: 9733035 Free PMC article.

8

Molecular breakpoint mapping of 6q11-q14 interstitial deletions in seven patients.

Wang JC, Dang L, Lomax B, Turner L, Shago M, Teebi AS, Klatt R, MacLeod PM, Yong SL, Nowaczyk MJ, Eydoux P. Wang JC, et al. Among authors: teebi as. Am J Med Genet A. 2009 Mar;149A(3):372-9. doi: 10.1002/ajmg.a.32675. Am J Med Genet A. 2009. PMID: 19213033

9

Congenital heart defects in Sotos syndrome.

Noreau DR, Al-Ata J, Jutras L, Teebi AS. Noreau DR, et al. Among authors: teebi as. Am J Med Genet. 1998 Oct 2;79(4):327-8. doi: 10.1002/(sici)1096-8628(19981002)79:4<327::aid-ajmg16>3.0.co;2-t. Am J Med Genet. 1998. PMID: 9781915

10

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

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