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G J Halpern

Showing results (11-20 of 25) with videos related to

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American Journal of Medical Genetics|March 17, 1997
Agenesis of the corpus callosum in a mother and sonD Inbar, G J Halpern, R Weitz, et al.
American Journal of Medical Genetics|June 26, 2001
Ectodermal dysplasia, ectrodactyly and macular dystrophy (EEM syndrome) in siblingsY Senecky, G J Halpern, D Inbar, et al.
American Journal of Medical Genetics|December 31, 1997
Further delineation of cerebro-osteo-nephrosis syndromeY Udler, G J Halpern, C Sher, et al.
American Journal of Medical Genetics|December 18, 2001
Fine mapping places the gene for arthrogryposis multiplex congenita neuropathic type between D5S394 and D5S2069 on chromosome 5qterM G Tanamy, N Magal, G J Halpern, et al.
Pediatric Radiology|February 9, 2000
Pathological fractures in spondyloenchondrodysplasia: case reportY Udler, G J Halpern, R S Lachman, et al.
The Israel Medical Association Journal : IMAJ|July 13, 2000
Prenatal diagnosis for detecting congenital malformations: acceptance among Israeli Arab womenL Jaber, T Dolfin, T Shohat, et al.
International Journal of Biometeorology|November 1, 1995
Solar activity cycle and the incidence of foetal chromosome abnormalities detected at prenatal diagnosisG J Halpern, E G Stoupel, G Barkai, et al.
The Israel Medical Association Journal : IMAJ|January 17, 2002
Autosomal dominant nephritis with renal failure of non-Alport type: clinical and molecular studiesT Ilan, T Shohat, A Tobar, et al.
American Journal of Medical Genetics|June 27, 2000
Increased transmission of intermediate alleles of the FMR1 gene compared with normal alleles among female heterozygotesV Drasinover, S Ehrlich, N Magal, et al.
Clinical Genetics|July 6, 2005
A putative new locus for an autosomal recessive cerebellar ataxia syndrome on chromosome 22q11H Baris, C Legum, L Levin, et al.
Pageof 3

Showing results (11-20 of 25) with videos related to

Sort By:
Pageof 3
American Journal of Medical Genetics|March 17, 1997
Agenesis of the corpus callosum in a mother and sonD Inbar, G J Halpern, R Weitz, et al.
American Journal of Medical Genetics|June 26, 2001
Ectodermal dysplasia, ectrodactyly and macular dystrophy (EEM syndrome) in siblingsY Senecky, G J Halpern, D Inbar, et al.
American Journal of Medical Genetics|December 31, 1997
Further delineation of cerebro-osteo-nephrosis syndromeY Udler, G J Halpern, C Sher, et al.
American Journal of Medical Genetics|December 18, 2001
Fine mapping places the gene for arthrogryposis multiplex congenita neuropathic type between D5S394 and D5S2069 on chromosome 5qterM G Tanamy, N Magal, G J Halpern, et al.
Pediatric Radiology|February 9, 2000
Pathological fractures in spondyloenchondrodysplasia: case reportY Udler, G J Halpern, R S Lachman, et al.
The Israel Medical Association Journal : IMAJ|July 13, 2000
Prenatal diagnosis for detecting congenital malformations: acceptance among Israeli Arab womenL Jaber, T Dolfin, T Shohat, et al.
International Journal of Biometeorology|November 1, 1995
Solar activity cycle and the incidence of foetal chromosome abnormalities detected at prenatal diagnosisG J Halpern, E G Stoupel, G Barkai, et al.
The Israel Medical Association Journal : IMAJ|January 17, 2002
Autosomal dominant nephritis with renal failure of non-Alport type: clinical and molecular studiesT Ilan, T Shohat, A Tobar, et al.
American Journal of Medical Genetics|June 27, 2000
Increased transmission of intermediate alleles of the FMR1 gene compared with normal alleles among female heterozygotesV Drasinover, S Ehrlich, N Magal, et al.
Clinical Genetics|July 6, 2005
A putative new locus for an autosomal recessive cerebellar ataxia syndrome on chromosome 22q11H Baris, C Legum, L Levin, et al.
Pageof 3