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R Carmi

Showing results (71-80 of 103) with videos related to

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American Journal of Medical Genetics|August 1, 1992
Weissenbacher-Zweymüller syndrome: a distinct autosomal recessive skeletal dysplasiaJ Chemke, R Carmi, A Galil, et al.
International Journal of Gynaecology and Obstetrics: the Official Organ of the International Federation of Gynaecology and Obstetrics|June 12, 1999
Maternal factors associated with severity of birth defectsE Sheiner, I Shoham-Vardi, E K Sheiner, et al.
European Journal of Pediatrics|August 1, 1988
Survival of a premature neonate with obstructive anuria due to Candida: the role of early sonographic diagnosis and antimycotic treatmentO Yadin, D Gradus Ben-Ezer, A Golan, et al.
Ophthalmic Genetics|June 1, 1995
A complex chromosome translocation resulting in deletion 11p and associated with uveal colobomataR Friling, Y Yassur, D Abeliovich, et al.
Harefuah|December 15, 1995
[Neurological symptoms associated with vitamin E deficiency]B A Sela, Z Shorer, R Doolman, et al.
American Journal of Human Genetics|August 1, 1996
An autosomal recessive nonsyndromic-hearing-loss locus identified by DNA pooling using two inbred Bedouin kindredsD A Scott, R Carmi, K Elbedour, et al.
Israel Journal of Medical Sciences|December 1, 1984
Adrenoleukodystrophy in Israel: a genetic, clinical and biochemical studyJ Chemke, E Lieberman, R Carmi, et al.
American Journal of Human Genetics|June 23, 1998
Homozygosity and linkage-disequilibrium mapping of the syndrome of congenital hypoparathyroidism, growth and mental retardation, and dysmorphism to a 1-cM interval on chromosome 1q42-43R Parvari, E Hershkovitz, A Kanis, et al.
Prenatal Diagnosis|March 22, 2001
Prenatal diagnosis of malignant osteopetrosis in Bedouin families by linkage analysisH Shalev, A Mishori-Dery, J Kapelushnik, et al.
American Journal of Medical Genetics|March 1, 1982
Aplasia cutis congenita in two sibs discordant for pyloric atresiaR Carmi, S Sofer, M Karplus, et al.
Pageof 11

Showing results (71-80 of 103) with videos related to

Sort By:
Pageof 11
American Journal of Medical Genetics|August 1, 1992
Weissenbacher-Zweymüller syndrome: a distinct autosomal recessive skeletal dysplasiaJ Chemke, R Carmi, A Galil, et al.
International Journal of Gynaecology and Obstetrics: the Official Organ of the International Federation of Gynaecology and Obstetrics|June 12, 1999
Maternal factors associated with severity of birth defectsE Sheiner, I Shoham-Vardi, E K Sheiner, et al.
European Journal of Pediatrics|August 1, 1988
Survival of a premature neonate with obstructive anuria due to Candida: the role of early sonographic diagnosis and antimycotic treatmentO Yadin, D Gradus Ben-Ezer, A Golan, et al.
Ophthalmic Genetics|June 1, 1995
A complex chromosome translocation resulting in deletion 11p and associated with uveal colobomataR Friling, Y Yassur, D Abeliovich, et al.
Harefuah|December 15, 1995
[Neurological symptoms associated with vitamin E deficiency]B A Sela, Z Shorer, R Doolman, et al.
American Journal of Human Genetics|August 1, 1996
An autosomal recessive nonsyndromic-hearing-loss locus identified by DNA pooling using two inbred Bedouin kindredsD A Scott, R Carmi, K Elbedour, et al.
Israel Journal of Medical Sciences|December 1, 1984
Adrenoleukodystrophy in Israel: a genetic, clinical and biochemical studyJ Chemke, E Lieberman, R Carmi, et al.
American Journal of Human Genetics|June 23, 1998
Homozygosity and linkage-disequilibrium mapping of the syndrome of congenital hypoparathyroidism, growth and mental retardation, and dysmorphism to a 1-cM interval on chromosome 1q42-43R Parvari, E Hershkovitz, A Kanis, et al.
Prenatal Diagnosis|March 22, 2001
Prenatal diagnosis of malignant osteopetrosis in Bedouin families by linkage analysisH Shalev, A Mishori-Dery, J Kapelushnik, et al.
American Journal of Medical Genetics|March 1, 1982
Aplasia cutis congenita in two sibs discordant for pyloric atresiaR Carmi, S Sofer, M Karplus, et al.
Pageof 11