Farag TI - Search Results

1

Kenny-Caffey syndrome in six Bedouin sibships: autosomal recessive inheritance is confirmed.

Tahseen K, Khan S, Uma R, Usha R, Al Ghanem MM, Al Awadi SA, Farag TI. Tahseen K, et al. Among authors: farag ti. Am J Med Genet. 1997 Mar 17;69(2):126-32. Am J Med Genet. 1997. PMID: 9056548

2

Late diagnosis of phenylketonuria in a Bedouin mother.

Usha R, Uma R, Farag TI, Girish Y, al-Ghanim MM, al-Najdi K, al-Awadi SA, el-Badramany MH. Usha R, et al. Among authors: farag ti. Am J Med Genet. 1992 Dec 1;44(6):713-5. doi: 10.1002/ajmg.1320440603. Am J Med Genet. 1992. PMID: 1481837

3

Phenotypic variability in Meckel-Gruber syndrome.

Farag TI, Usha R, Uma R, Mady SA, al-Nagdy K, el-Badramany MH. Farag TI, et al. Clin Genet. 1990 Sep;38(3):176-9. doi: 10.1111/j.1399-0004.1990.tb03568.x. Clin Genet. 1990. PMID: 2225527

4

Direct duplication of chromosome 1, dir dup(1)(p21.2----p32) in a Bedouin boy with multiple congenital anomalies.

Mohammed FM, Farag TI, Gunawardana SS, al-Digashim DD, al-Awadi SA, al-Othman SA, Sundareshan TS. Mohammed FM, et al. Among authors: farag ti. Am J Med Genet. 1989 Mar;32(3):353-5. doi: 10.1002/ajmg.1320320316. Am J Med Genet. 1989. PMID: 2729356

5

Familial uterine hernia syndrome: report of an Arab family with four affected males.

Naguib KK, Teebi AS, Farag TI, al-Awadi SA, el-Khalifa MY, el-Sayed Mahfouz. Naguib KK, et al. Among authors: farag ti. Am J Med Genet. 1989 Jun;33(2):180-1. doi: 10.1002/ajmg.1320330208. Am J Med Genet. 1989. PMID: 2764027

6

Macrosomia, microphthalmia, +/- cleft palate and early infant death: a new autosomal recessive syndrome.

Teebi AS, al-Saleh QA, Hassoon MM, Farag TI, al-Awadi SA. Teebi AS, et al. Among authors: farag ti. Clin Genet. 1989 Sep;36(3):174-7. doi: 10.1111/j.1399-0004.1989.tb03184.x. Clin Genet. 1989. PMID: 2791331

7

A family with spondyloepimetaphyseal dwarfism: a 'new' dysplasia or Kniest disease with autosomal recessive inheritance?

Farag TI, Al-Awadi SA, Hunt MC, Satyanath S, Zahran M, Usha R, Uma R. Farag TI, et al. J Med Genet. 1987 Oct;24(10):597-601. doi: 10.1136/jmg.24.10.597. J Med Genet. 1987. PMID: 3681904 Free PMC article.

8

Nonsyndromal anencephaly: possible autosomal recessive variant.

Farag TI, Teebi AS, Al-Awadi SA. Farag TI, et al. Am J Med Genet. 1986 Jul;24(3):461-4. doi: 10.1002/ajmg.1320240308. Am J Med Genet. 1986. PMID: 3728564

9

Second family with "apple peel" syndrome affecting four siblings: autosomal recessive inheritance confirmed.

Farag TI, al-Awadi SA, el-Badramany MH, Usha R, el-Ghanem M. Farag TI, et al. Am J Med Genet. 1993 Aug 1;47(1):119-21. doi: 10.1002/ajmg.1320470126. Am J Med Genet. 1993. PMID: 8368241 No abstract available.

10

The newly recognised limb/pelvis-hypoplasia/aplasia syndrome: report of a Bedouin patient and review.

Farag TI, al-Awadi SA, Marafie MJ, Bastaki L, al-Othman SA, Mohammed FM, AlSuliman IS, Murthy DS. Farag TI, et al. J Med Genet. 1993 Jan;30(1):62-4. doi: 10.1136/jmg.30.1.62. J Med Genet. 1993. PMID: 8423610 Free PMC article. Review.

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