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Results:
1-10
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Results: 10
Authors:
Hasan, MA
Batieha, A
Jadou, H
Khawaldeh, AK
Ajlouni, K
Citation: Ma. Hasan et al., Growth status of Jordanian schoolchildren in military-funded schools, EUR J CL N, 55(5), 2001, pp. 380-386
Authors:
Al-Sheyyab, M
Jarrah, N
Younis, E
Shennak, MM
Hadidi, A
Awidi, A
El-Shanti, H
Ajlouni, K
Citation: M. Al-sheyyab et al., Bleeding tendency in Wolfram syndrome: a newly identified feature with phenotype genotype correlation, EUR J PED, 160(4), 2001, pp. 243-246
Authors:
Jarrah, N
El-Shanti, H
Khier, A
Obeidat, FN
Haddidi, A
Ajlouni, K
Citation: N. Jarrah et al., Familial disorder of sex determination in seven individuals from three related sibships, EUR J PED, 159(12), 2000, pp. 912-918
Authors:
Batieha, A
Jaddou, H
Ajlouni, K
Citation: A. Batieha et al., The performance of the revised criterion for diagnosis of diabetes melilitus in Jordan, ANN SAUDI M, 20(2), 2000, pp. 168-169
Authors:
El-Shanti, H
Lidral, AC
Marazita, ML
Cooper, ME
Jarrah, N
Druhan, L
Ajlouni, K
Citation: H. El-shanti et al., Homozygosity mapping identifies an additional locus for Wolfram syndrome on chromosome 4q (vol 66, pg 1229, 2000), AM J HU GEN, 66(5), 2000, pp. 1728-1728
Authors:
El-Shanti, H
Lidral, AC
Jarrah, N
Druhan, L
Ajlouni, K
Citation: H. El-shanti et al., Homozygosity mapping identifies an additional locus for Wolfram syndrome on chromosome 4q, AM J HU GEN, 66(4), 2000, pp. 1229-1236
Authors:
Al-Qadreh, A
Ajlouni, K
Citation: A. Al-qadreh et K. Ajlouni, Proceedings of the First Workshop on Insulin-Dependent Diabetes Mellitus in Children and Adolescents - Amman, Jordan - 26-28 October 1997 - Foreword, ACT PAEDIAT, 88, 1999, pp. 1-1
Authors:
Ajlouni, K
Qusous, Y
Khawaldeh, AK
Jaddou, H
Batiehah, A
Ammari, F
Zaheri, M
Mashal, A
Citation: K. Ajlouni et al., Incidence of insulin-dependent diabetes mellitus in Jordanian children aged 0-14 y during 1992-1996, ACT PAEDIAT, 88, 1999, pp. 11-13
Authors:
El-Shanti, H
Al-Salem, M
El-Najjar, M
Ajlouni, K
Beck, J
Sheffield, VC
Stone, EM
Citation: H. El-shanti et al., A nonsense mutation in the retinal specific guanylate cyclase gene is the cause of Leber congenital amaurosis in a large inbred kindred from Jordan, J MED GENET, 36(11), 1999, pp. 862-865
Authors:
Younis, E
Jarrah, N
Abdeen, G
Raqqad, A
Tarawneh, M
Ajlouni, K
Citation: E. Younis et al., Anorexia nervosa with pancytopenia, ANN SAUDI M, 18(5), 1998, pp. 478-479
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1-10
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