Teebi AS - Search Results

1

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.

2

Total anonychia congenita and microcephaly with normal intelligence: a new autosomal-recessive syndrome?

Teebi AS, Kaurah P. Teebi AS, et al. Am J Med Genet. 1996 Dec 18;66(3):257-60. doi: 10.1002/(SICI)1096-8628(19961218)66:3<257::AID-AJMG3>3.0.CO;2-M. Am J Med Genet. 1996. PMID: 8985482

3

Severe hypertelorism, midface prominence, prominent/simple ears, severe myopia, borderline intelligence, and bone fragility in two brothers: new syndrome?

Hamamy HA, Teebi AS, Oudjhane K, Shegem NN, Ajlouni KM. Hamamy HA, et al. Among authors: teebi as. Am J Med Genet A. 2007 Feb 1;143A(3):229-34. doi: 10.1002/ajmg.a.31594. Am J Med Genet A. 2007. PMID: 17230486

4

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

5

Dyskeratosis congenita: an autosomal recessive variant.

Elliott AM, Graham GE, Bernstein M, Mazer B, Teebi AS. Elliott AM, et al. Among authors: teebi as. Am J Med Genet. 1999 Mar 19;83(3):178-82. doi: 10.1002/(sici)1096-8628(19990319)83:3<178::aid-ajmg6>3.0.co;2-3. Am J Med Genet. 1999. PMID: 10096592

6

Choanal and ileal atresia: a new syndrome or association?

Yoskovitch A, Tewfik TL, Nguyen L, Oudjhane K, Teebi AS. Yoskovitch A, et al. Among authors: teebi as. Int J Pediatr Otorhinolaryngol. 1999 Aug 20;49(3):237-40. doi: 10.1016/s0165-5876(99)00196-2. Int J Pediatr Otorhinolaryngol. 1999. PMID: 10519704

7

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.

8

Autosomal recessive Robinow syndrome.

Teebi AS. Teebi AS. Am J Med Genet. 1990 Jan;35(1):64-8. doi: 10.1002/ajmg.1320350112. Am J Med Genet. 1990. PMID: 2301471

9

New autosomal recessive faciodigitogenital syndrome.

Teebi AS, Naguib KK, Al-Awadi S, Al-Saleh QA. Teebi AS, et al. J Med Genet. 1988 Jun;25(6):400-6. doi: 10.1136/jmg.25.6.400. J Med Genet. 1988. PMID: 3398008 Free PMC article.

10

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

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