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O Reish

Showing results (11-20 of 27) with videos related to

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American Journal of Medical Genetics|January 2, 1996
Duplication of 7p: further delineation of the phenotype and restriction of the critical region to the distal part of the short armO Reish, S A Berry, G Dewald, et al.
Chromosome Research : an International Journal on the Molecular, Supramolecular and Evolutionary Aspects of Chromosome Biology|January 10, 2002
Replication status as a possible marker for genomic instability in cells originating from genotypes with balanced rearrangementsA Amiel, E Levi, O Reish, et al.
Ultrasound in Obstetrics & Gynecology : the Official Journal of the International Society of Ultrasound in Obstetrics and Gynecology|July 1, 2005
Is there an increased rate of megacystis in twins?R Maymon, I Ben-Ami, Z Vaknin, et al.
Journal of Medical Genetics|September 1, 1995
The molecular basis of ornithine transcarbamylase deficiency: modelling the human enzyme and the effects of mutationsM Tuchman, H Morizono, O Reish, et al.
European Journal of Pediatric Surgery : Official Journal of Austrian Association of Pediatric Surgery ... [Et Al] = Zeitschrift Fur Kinderchirurgie|November 24, 2001
Congenital short-bowel and malrotation: clinical presentation and outcome of six affected offspring in three related familiesI Erez, O Reish, M Kovalivker, et al.
American Journal of Medical Genetics|April 29, 1998
Dilemma of trisomy 20 mosaicism detected prenatally: is it an innocent finding?O Reish, B Wolach, A Amiel, et al.
Chromosome Research : an International Journal on the Molecular, Supramolecular and Evolutionary Aspects of Chromosome Biology|April 26, 2000
Replication asynchrony increases in women at risk for aneuploid offspringA Amiel, O Reish, E Gaber, et al.
American Journal of Human Genetics|July 1, 1995
Tyrosinase inhibition due to interaction of homocyst(e)ine with copper: the mechanism for reversible hypopigmentation in homocystinuria due to cystathionine beta-synthase deficiencyO Reish, D Townsend, S A Berry, et al.
Prenatal Diagnosis|September 1, 1996
Are all phenotypically-normal Turner syndrome fetuses mosaics?A Amiel, D Kidron, I Kedar, 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.
Pageof 3

Showing results (11-20 of 27) with videos related to

Sort By:
Pageof 3
American Journal of Medical Genetics|January 2, 1996
Duplication of 7p: further delineation of the phenotype and restriction of the critical region to the distal part of the short armO Reish, S A Berry, G Dewald, et al.
Chromosome Research : an International Journal on the Molecular, Supramolecular and Evolutionary Aspects of Chromosome Biology|January 10, 2002
Replication status as a possible marker for genomic instability in cells originating from genotypes with balanced rearrangementsA Amiel, E Levi, O Reish, et al.
Ultrasound in Obstetrics & Gynecology : the Official Journal of the International Society of Ultrasound in Obstetrics and Gynecology|July 1, 2005
Is there an increased rate of megacystis in twins?R Maymon, I Ben-Ami, Z Vaknin, et al.
Journal of Medical Genetics|September 1, 1995
The molecular basis of ornithine transcarbamylase deficiency: modelling the human enzyme and the effects of mutationsM Tuchman, H Morizono, O Reish, et al.
European Journal of Pediatric Surgery : Official Journal of Austrian Association of Pediatric Surgery ... [Et Al] = Zeitschrift Fur Kinderchirurgie|November 24, 2001
Congenital short-bowel and malrotation: clinical presentation and outcome of six affected offspring in three related familiesI Erez, O Reish, M Kovalivker, et al.
American Journal of Medical Genetics|April 29, 1998
Dilemma of trisomy 20 mosaicism detected prenatally: is it an innocent finding?O Reish, B Wolach, A Amiel, et al.
Chromosome Research : an International Journal on the Molecular, Supramolecular and Evolutionary Aspects of Chromosome Biology|April 26, 2000
Replication asynchrony increases in women at risk for aneuploid offspringA Amiel, O Reish, E Gaber, et al.
American Journal of Human Genetics|July 1, 1995
Tyrosinase inhibition due to interaction of homocyst(e)ine with copper: the mechanism for reversible hypopigmentation in homocystinuria due to cystathionine beta-synthase deficiencyO Reish, D Townsend, S A Berry, et al.
Prenatal Diagnosis|September 1, 1996
Are all phenotypically-normal Turner syndrome fetuses mosaics?A Amiel, D Kidron, I Kedar, 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.
Pageof 3