Rajab A - Search Results

1

PRUNE is crucial for normal brain development and mutated in microcephaly with neurodevelopmental impairment.

Zollo M, Ahmed M, Ferrucci V, Salpietro V, Asadzadeh F, Carotenuto M, Maroofian R, Al-Amri A, Singh R, Scognamiglio I, Mojarrad M, Musella L, Duilio A, Di Somma A, Karaca E, Rajab A, Al-Khayat A, Mohan Mohapatra T, Eslahi A, Ashrafzadeh F, Rawlins LE, Prasad R, Gupta R, Kumari P, Srivastava M, Cozzolino F, Kumar Rai S, Monti M, Harlalka GV, Simpson MA, Rich P, Al-Salmi F, Patton MA, Chioza BA, Efthymiou S, Granata F, Di Rosa G, Wiethoff S, Borgione E, Scuderi C, Mankad K, Hanna MG, Pucci P, Houlden H, Lupski JR, Crosby AH, Baple EL. Zollo M, et al. Among authors: rajab a. Brain. 2017 Apr 1;140(4):940-952. doi: 10.1093/brain/awx014. Brain. 2017. PMID: 28334956 Free PMC article.

2

Loss of PCLO function underlies pontocerebellar hypoplasia type III.

Ahmed MY, Chioza BA, Rajab A, Schmitz-Abe K, Al-Khayat A, Al-Turki S, Baple EL, Patton MA, Al-Memar AY, Hurles ME, Partlow JN, Hill RS, Evrony GD, Servattalab S, Markianos K, Walsh CA, Crosby AH, Mochida GH. Ahmed MY, et al. Among authors: rajab a. Neurology. 2015 Apr 28;84(17):1745-50. doi: 10.1212/WNL.0000000000001523. Epub 2015 Apr 1. Neurology. 2015. PMID: 25832664 Free PMC article.

3

A study of consanguinity in the Sultanate of Oman.

Rajab A, Patton MA. Rajab A, et al. Ann Hum Biol. 2000 May-Jun;27(3):321-6. doi: 10.1080/030144600282208. Ann Hum Biol. 2000. PMID: 10834296

4

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

5

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

6

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

7

Neural tube defects and congenital hydrocephalus in the Sultanate of Oman.

Rajab A, Vaishnav A, Freeman NV, Patton MA. Rajab A, et al. J Trop Pediatr. 1998 Oct;44(5):300-3. doi: 10.1093/tropej/44.5.300. J Trop Pediatr. 1998. PMID: 9819495

8

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

9

The frequency of posterior urethral valves in Oman.

Rajab A, Freeman NV, Patton M. Rajab A, et al. Br J Urol. 1996 Jun;77(6):900-4. doi: 10.1046/j.1464-410x.1996.98624.x. Br J Urol. 1996. PMID: 8705230

10

Further delineation of the DOOR syndrome.

Rajab A, Riaz A, Paul G, Al-Khusaibi S, Chalmers R, Patton MA. Rajab A, et al. Clin Dysmorphol. 2000 Oct;9(4):247-51. doi: 10.1097/00019605-200009040-00003. Clin Dysmorphol. 2000. PMID: 11045579

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