Rajab A - Search Results

1

Recessive Robinow syndrome, allelic to dominant brachydactyly type B, is caused by mutation of ROR2.

Afzal AR, Rajab A, Fenske CD, Oldridge M, Elanko N, Ternes-Pereira E, Tüysüz B, Murday VA, Patton MA, Wilkie AO, Jeffery S. Afzal AR, et al. Among authors: rajab a. Nat Genet. 2000 Aug;25(4):419-22. doi: 10.1038/78107. Nat Genet. 2000. PMID: 10932186

2

Linkage of recessive Robinow syndrome to a 4 cM interval on chromosome 9q22.

Afzal AR, Rajab A, Fenske C, Crosby A, Lahiri N, Ternes-Pereira E, Murday VA, Houlston R, Patton MA, Jeffery S. Afzal AR, et al. Among authors: rajab a. Hum Genet. 2000 Mar;106(3):351-4. doi: 10.1007/s004390051049. Hum Genet. 2000. PMID: 10798366

3

Analysis of the population structure in Oman.

Rajab A, Patton MA. Rajab A, et al. Community Genet. 1999;2(1):23-5. doi: 10.1159/000016179. Community Genet. 1999. PMID: 15178958

4

Heterogeneity for congenital generalized lipodystrophy in seventeen patients from Oman.

Rajab A, Heathcote K, Joshi S, Jeffery S, Patton M. Rajab A, et al. Am J Med Genet. 2002 Jul 1;110(3):219-25. doi: 10.1002/ajmg.10437. Am J Med Genet. 2002. PMID: 12116229

5

Molecular analysis of Berardinelli-Seip congenital lipodystrophy in Oman: evidence for multiple loci.

Heathcote K, Rajab A, Magré J, Syrris P, Besti M, Patton M, Délépine M, Lathrop M, Capeau J, Jeffery S. Heathcote K, et al. Among authors: rajab a. Diabetes. 2002 Apr;51(4):1291-3. doi: 10.2337/diabetes.51.4.1291. Diabetes. 2002. PMID: 11916958

6

Major factors determining the frequencies of hemoglobinopathies in Oman.

Rajab A, Patton MA. Rajab A, et al. Am J Med Genet. 1997 Aug 8;71(2):240-2. doi: 10.1002/(sici)1096-8628(19970808)71:2<240::aid-ajmg26>3.0.co;2-d. Am J Med Genet. 1997. PMID: 9217233 No abstract available.

7

Development and use of a national haemoglobinopathy register in Oman.

Rajab A, Patton MA. Rajab A, et al. Community Genet. 1999;2(1):47-8. doi: 10.1159/000016185. Community Genet. 1999. PMID: 15178963 No abstract available.

8

A gradient of ROR2 protein stability and membrane localization confers brachydactyly type B or Robinow syndrome phenotypes.

Schwarzer W, Witte F, Rajab A, Mundlos S, Stricker S. Schwarzer W, et al. Among authors: rajab a. Hum Mol Genet. 2009 Nov 1;18(21):4013-21. doi: 10.1093/hmg/ddp345. Epub 2009 Jul 29. Hum Mol Genet. 2009. PMID: 19640924

9

Study of hemoglobinopathies in Oman through a national register.

Rajab AG, Patton MA, Modell B. Rajab AG, et al. Saudi Med J. 2000 Dec;21(12):1168-72. Saudi Med J. 2000. PMID: 11360093

10

Hirschsprung's disease in Oman.

Rajab A, Freeman NV, Patton MA. Rajab A, et al. J Pediatr Surg. 1997 May;32(5):724-7. doi: 10.1016/s0022-3468(97)90015-4. J Pediatr Surg. 1997. PMID: 9165461

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