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J Dagan

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

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American Journal of Medical Genetics|December 2, 1996
t(15;21)(q15;q22.1) pat resulting in partial trisomy and partial monosomy of chromosomes 15 and 21 in two offspringD Abeliovich, J Dagan, I Lerer, et al.
European Journal of Human Genetics : EJHG|February 5, 1998
Transient neonatal diabetes mellitus in a child with invdup(6)(q22q23) of paternal originE I Arthur, J Zlotogora, I Lerer, et al.
Cytogenetics and Cell Genetics|January 1, 1978
A long unidentifiable extra chromosomal segment--a possible duplication of human 7qJ Wahrman, M M Cohen, A Rosenmann, et al.
Journal of Medical Genetics|December 1, 1984
A complex three way translocation resulting in two sibs with partial trisomy 3p23----3pterR Voss, E Gross-Kieselstein, H Hurvitz, et al.
Journal of Medical Genetics|November 14, 1997
A syndrome including thumb malformations, microcephaly, short stature, and hypogonadismJ Zlotogora, J Dagan, A Ganen, 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.
Clinical Genetics|August 1, 1986
Partial deletion of the short arm of chromosome 3: further delineation of the 3p25-3pter syndromeR M Reifen, R Gale, E Kerem, et al.
Medical & Biological Engineering & Computing|May 1, 1981
MYO-MAP--a fast recording system for epicardial mappingJ Dagan, A Battler, L Adam, et al.
American Journal of Human Genetics|September 1, 1989
Isodisomy of chromosome 7 in a patient with cystic fibrosis: could uniparental disomy be common in humans?R Voss, E Ben-Simon, A Avital, et al.
Genomics|February 1, 1991
The ATC (ataxia-telangiectasia complementation group C) locus localizes to 11q22-q23Y Ziv, G Rotman, M Frydman, et al.
Pageof 3

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

Sort By:
Pageof 3
You have reached the last page of results.This site can display upto 30 results.
American Journal of Medical Genetics|December 2, 1996
t(15;21)(q15;q22.1) pat resulting in partial trisomy and partial monosomy of chromosomes 15 and 21 in two offspringD Abeliovich, J Dagan, I Lerer, et al.
European Journal of Human Genetics : EJHG|February 5, 1998
Transient neonatal diabetes mellitus in a child with invdup(6)(q22q23) of paternal originE I Arthur, J Zlotogora, I Lerer, et al.
Cytogenetics and Cell Genetics|January 1, 1978
A long unidentifiable extra chromosomal segment--a possible duplication of human 7qJ Wahrman, M M Cohen, A Rosenmann, et al.
Journal of Medical Genetics|December 1, 1984
A complex three way translocation resulting in two sibs with partial trisomy 3p23----3pterR Voss, E Gross-Kieselstein, H Hurvitz, et al.
Journal of Medical Genetics|November 14, 1997
A syndrome including thumb malformations, microcephaly, short stature, and hypogonadismJ Zlotogora, J Dagan, A Ganen, 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.
Clinical Genetics|August 1, 1986
Partial deletion of the short arm of chromosome 3: further delineation of the 3p25-3pter syndromeR M Reifen, R Gale, E Kerem, et al.
Medical & Biological Engineering & Computing|May 1, 1981
MYO-MAP--a fast recording system for epicardial mappingJ Dagan, A Battler, L Adam, et al.
American Journal of Human Genetics|September 1, 1989
Isodisomy of chromosome 7 in a patient with cystic fibrosis: could uniparental disomy be common in humans?R Voss, E Ben-Simon, A Avital, et al.
Genomics|February 1, 1991
The ATC (ataxia-telangiectasia complementation group C) locus localizes to 11q22-q23Y Ziv, G Rotman, M Frydman, et al.
Pageof 3