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Results:
1-15
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Results: 15
Authors:
Mahafza, T
El-Shanti, H
Omari, H
Citation: T. Mahafza et al., Raine syndrome: report of a case with hand and foot anomalies, CLIN DYSMOR, 10(3), 2001, pp. 227-229
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:
Majeed, HA
Al-Tarawna, M
El-Shanti, H
Kamel, B
Al-Khalaileh, F
Citation: Ha. Majeed et al., The syndrome of chronic recurrent multifocal osteomyelitis and congenital dyserythropoietic anaemia. Report of a new family and a review, EUR J PED, 160(12), 2001, pp. 705-710
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:
Majeed, HA
El-Shanti, H
Al-Rimawi, H
Al-Masri, N
Citation: Ha. Majeed et al., On mice and men: An autosomal recessive syndrome of chronic recurrent multifocal osteomyelitis and congenital dyserythropoietic anemia, J PEDIAT, 137(3), 2000, pp. 441-442
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:
Majeed, HA
Rawashdeh, M
El-Shanti, H
Qubain, H
Khuri-Bulos, N
Shahin, HM
Citation: Ha. Majeed et al., Familial Mediterranean fever in children: the expanded clinical profile (vol 92, pg 309, 1999), QJM-MON J A, 92(9), 1999, pp. 545-545
Authors:
Majeed, HA
Rawashdeh, M
El-Shanti, H
Qubain, H
Khuribulos, N
Shahin, HM
Citation: Ha. Majeed et al., Familial Mediterranean fever in children: the expanded clinical profile, QJM-MON J A, 92(6), 1999, pp. 309-318
Authors:
Hurvitz, JR
Suwairi, WM
Van Hul, W
El-Shanti, H
Superti-Furga, A
Roudier, J
Holderbaum, D
Pauli, RM
Herd, JK
Van Hul, E
Rezai-Delui, H
Legius, E
Le Merrer, M
Al-Alami, J
Bahabri, SA
Warman, ML
Citation: Jr. Hurvitz et al., Mutations in the CCN gene family member WISP3 cause progressive pseudorheumatoid dysplasia, NAT GENET, 23(1), 1999, pp. 94-98
Authors:
Al-Sheyyab, M
Batieha, A
El-Shanti, H
Daoud, A
Citation: M. Al-sheyyab et al., Henoch-Schonlein purpura and streptococcal infection: a prospective case-control study, ANN TROP PA, 19(3), 1999, pp. 253-255
Authors:
Jarrah, NS
El-Shanti, H
Shennak, MM
Ajlouni, KM
Citation: Ns. Jarrah et al., A case of Wolfram syndrome in triplets: Some newly recognized features, ANN SAUDI M, 19(2), 1999, pp. 132-134
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:
Al-Rimawi, HS
Al-Sheyyab, M
Batieha, A
El-Shanti, H
Abuekteish, F
Citation: Hs. Al-rimawi et al., Effect of desferrioxamine in acute haemolytic anaemia of glucose-6-phosphate dehydrogenase deficiency, ACT HAEMAT, 101(3), 1999, pp. 145-148
Authors:
El-Shanti, H
Al-Lahham, M
Batieha, A
Citation: H. El-shanti et al., Normative standards of trunk and limb anthropometric measurements in Jordanian newborns, SAUDI MED J, 19(6), 1998, pp. 702-706
Risultati:
1-15
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