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O Reish

Showing results (21-30 of 27) with videos related to

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The Pediatric Infectious Disease Journal|December 1, 1990
Mumps arthritis in childrenL Harel, J Amir, O Reish, et al.
American Journal of Medical Genetics|February 11, 1997
Brain anomalies, retardation of mentality and growth, ectodermal dysplasia, skeletal malformations, Hirschsprung disease, ear deformity and deafness, eye hypoplasia, cleft palate, cryptorchidism, and kidney dysplasia/hypoplasia (BRESEK/BRESHECK): new X-linked syndrome?O Reish, R J Gorlin, M Hordinsky, et al.
Harefuah|October 8, 2014
[Prenatal diagnosis of trisomy 13 and trisomy 18: the experience of Assaf-Harofe Medical Center]M Naor Dovev, R Maymon, R Keidar, et al.
Journal of Inherited Metabolic Disease|May 10, 2002
Glu274Lys/Gly309Arg mutation of the tissue-nonspecific alkaline phosphatase gene in neonatal hypophosphatasia associated with convulsionsLitmanovitz, O Reish, T Dolfin, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|May 5, 2001
Molecular analysis of an extended Palestinian family from Israel with monilethrixW S Oetting, J P Fryer, Z Wyman, et al.
Blood Cancer Journal|October 16, 2012
The increased expression of 14q32 small nucleolar RNA transcripts in promyelocytic leukemia cells is not dependent on PML-RARA fusion geneY Cohen, K Hertzog, O Reish, et al.
Clinical Genetics|April 19, 2011
Screening and cell-based assessment of mutations in the Aristaless-related homeobox (ARX) geneT Fullston, M Finnis, A Hackett, et al.
Pageof 3

Showing results (21-30 of 27) with videos related to

Sort By:
Pageof 3
You have reached the last page of results.This site can display upto 27 results.
The Pediatric Infectious Disease Journal|December 1, 1990
Mumps arthritis in childrenL Harel, J Amir, O Reish, et al.
American Journal of Medical Genetics|February 11, 1997
Brain anomalies, retardation of mentality and growth, ectodermal dysplasia, skeletal malformations, Hirschsprung disease, ear deformity and deafness, eye hypoplasia, cleft palate, cryptorchidism, and kidney dysplasia/hypoplasia (BRESEK/BRESHECK): new X-linked syndrome?O Reish, R J Gorlin, M Hordinsky, et al.
Harefuah|October 8, 2014
[Prenatal diagnosis of trisomy 13 and trisomy 18: the experience of Assaf-Harofe Medical Center]M Naor Dovev, R Maymon, R Keidar, et al.
Journal of Inherited Metabolic Disease|May 10, 2002
Glu274Lys/Gly309Arg mutation of the tissue-nonspecific alkaline phosphatase gene in neonatal hypophosphatasia associated with convulsionsLitmanovitz, O Reish, T Dolfin, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|May 5, 2001
Molecular analysis of an extended Palestinian family from Israel with monilethrixW S Oetting, J P Fryer, Z Wyman, et al.
Blood Cancer Journal|October 16, 2012
The increased expression of 14q32 small nucleolar RNA transcripts in promyelocytic leukemia cells is not dependent on PML-RARA fusion geneY Cohen, K Hertzog, O Reish, et al.
Clinical Genetics|April 19, 2011
Screening and cell-based assessment of mutations in the Aristaless-related homeobox (ARX) geneT Fullston, M Finnis, A Hackett, et al.
Pageof 3