AAAAAA
Results:
1-15
|
Results: 15
Authors:
Ilan, T
Shohat, T
Tobar, A
Magal, N
Yahav, M
Halpern, GJ
Rechavi, G
Shohat, M
Citation: T. Ilan et al., Autosomal dominant nephritis with renal failure of non-alport type: Clinical and molecular studies, ISR MED ASS, 3(7), 2001, pp. 488-491
Authors:
Tanamy, MG
Magal, N
Halpern, GJ
Jaber, L
Shohat, M
Citation: Mg. Tanamy et al., Fine mapping places the gene for arthrogryposis multiplex congenita neuropathic type between D5S394 and D5S2069 on chromosome 5qter, AM J MED G, 104(2), 2001, pp. 152-156
Authors:
Udler, Y
Kauschansky, A
Yeshaya, J
Freedman, J
Barkai, U
Tobar, A
Okon, E
Halpern, GJ
Shohat, M
Legum, C
Citation: Y. Udler et al., Phenotypic expression of tissue mosaicism in a 45,X/46,X,dicY(q11.2) female, AM J MED G, 102(4), 2001, pp. 318-323
Authors:
Senecky, Y
Halpern, GJ
Inbar, D
Attias, J
Shohat, M
Citation: Y. Senecky et al., Ectodermal dysplasia, ectrodactyly and macular dystrophy (EEM syndrome) insiblings, AM J MED G, 101(3), 2001, pp. 195-197
Authors:
Halpern, GJ
Mimouni, A
Shohat, M
Citation: Gj. Halpern et al., E148Q of the MEFV gene causes amyloidosis in familial Mediterranean fever patients - Reply, PEDIATRICS, 108(1), 2001, pp. 215-215
Authors:
Toledano-Alhadef, H
Basel-Vanagaite, L
Magal, N
Davidov, B
Ehrlich, S
Drasinover, V
Taub, E
Halpern, GJ
Ginott, N
Shohat, M
Citation: H. Toledano-alhadef et al., Fragile-X carrier screening and the prevalence of premutation and full-mutation carriers in Israel, AM J HU GEN, 69(2), 2001, pp. 351-360
Authors:
Jaber, L
Dolfin, T
Shohat, T
Halpern, GJ
Reish, O
Fejgin, M
Citation: L. Jaber et al., Prenatal diagnosis for detecting congenital malformations: Acceptance among Israeli Arab women, ISR MED ASS, 2(5), 2000, pp. 346-350
Authors:
Stoffman, N
Magal, N
Shohat, T
Lotan, R
Koman, S
Oron, A
Danon, Y
Halpern, GJ
Lifshitz, Y
Shohat, M
Citation: N. Stoffman et al., Higher than expected carrier rates for familial Mediterranean fever in various Jewish ethnic groups, EUR J HUM G, 8(4), 2000, pp. 307-310
Authors:
Udler, Y
Halpern, GJ
Lachman, RS
Rimoin, DL
Shohat, M
Citation: Y. Udler et al., Pathological fractures in spondyloenchondrodysplasia: case report, PEDIAT RAD, 30(2), 2000, pp. 119-120
Authors:
Drasinover, V
Ehrlich, S
Magal, N
Taub, E
Libman, V
Shohat, T
Halpern, GJ
Shohat, M
Citation: V. Drasinover et al., Increased transmission of intermediate alleles of the FMR1 gene compared with normal alleles among female heterozygotes, AM J MED G, 93(2), 2000, pp. 155-157
Authors:
Mimouni, A
Magal, N
Stoffman, N
Shohat, T
Minasian, A
Krasnov, M
Halpern, GJ
Rotter, JI
Fischel-Ghodsian, N
Danon, YL
Shohat, M
Citation: A. Mimouni et al., Familial Mediterranean fever: Effects of genotype and ethnicity on inflammatory attacks and amyloidosis, PEDIATRICS, 105(5), 2000, pp. E701-E707
Authors:
Jaber, L
Halpern, GJ
Shohat, T
Citation: L. Jaber et al., Trends in the frequencies of consanguineous marriages in the Israeli Arab community, CLIN GENET, 58(2), 2000, pp. 106-110
Authors:
Shohat, M
Magal, N
Shohat, T
Chen, X
Dagan, T
Mimouni, A
Danon, Y
Lotan, R
Ogur, G
Sirin, A
Schlezinger, M
Halpern, GJ
Schwabe, A
Kastner, D
Rotter, JI
Fischel-Ghodsian, N
Citation: M. Shohat et al., Phenotype-genotype correlation in familial Mediterranean fever: evidence for an association between Met694Val and amyloidosis, EUR J HUM G, 7(3), 1999, pp. 287-292
Authors:
Shohat, M
Fischel-Ghodsian, N
Legum, C
Halpern, GJ
Citation: M. Shohat et al., Aminoglycoside-induced deafness associated with the mitochondrial DNA mutation A1555G, AM J OTOLAR, 20(1), 1999, pp. 64-67
Authors:
Udler, Y
Halpern, GJ
Shohat, M
Cohen, D
Citation: Y. Udler et al., Tsukahara syndrome of radioulnar synostosis, short stature, microcephaly, scoliosis, and mental retardation, AM J MED G, 80(5), 1998, pp. 526-528
Risultati:
1-15
|