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R Wallerstein

Showing results (21-30 of 29) with videos related to

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Clinical Genetics|May 23, 2006
Factors in decision making following genetic counseling for pre-natal diagnosis of de novo chromosomal rearrangementsR Wallerstein, V Strmen, J Durcan, et al.
Clinical Genetics|August 8, 2009
Copy number variations in three children with sudden infant deathG A Toruner, R Kurvathi, R Sugalski, et al.
Journal of Medical Genetics|March 1, 1997
Submicroscopic deletions at 16p13.3 in Rubinstein-Taybi syndrome: frequency and clinical manifestations in a North American populationR Wallerstein, C E Anderson, B Hay, et al.
American Journal of Medical Genetics|June 13, 1997
Lateral meningocele syndrome: three new patients and review of the literatureK W Gripp, C I Scott, H E Hughes, et al.
Clinical Genetics|September 7, 2016
Further evidence that de novo missense and truncating variants in ZBTB18 cause intellectual disability with variable featuresJ S Cohen, S Srivastava, K D Farwell Hagman, et al.
Proceedings of the National Academy of Sciences of the United States of America|April 25, 2002
Slowed conduction and ventricular tachycardia after targeted disruption of the cardiac sodium channel gene Scn5aG Alex Papadatos, Polly M R Wallerstein, Catherine E G Head, et al.
Journal of Medical Genetics|March 4, 2000
Diagnostic analysis of the Rubinstein-Taybi syndrome: five cosmids should be used for microdeletion detection and low number of protein truncating mutationsF Petrij, H G Dauwerse, R I Blough, et al.
American Journal of Human Genetics|May 20, 1999
The spectrum of mutations in TBX3: Genotype/Phenotype relationship in ulnar-mammary syndromeM Bamshad, T Le, W S Watkins, et al.
Prenatal Diagnosis|March 1, 2000
Common trisomy mosaicism diagnosed in amniocytes involving chromosomes 13, 18, 20 and 21: karyotype-phenotype correlationsR Wallerstein, M T Yu, R L Neu, et al.
Pageof 3

Showing results (21-30 of 29) with videos related to

Sort By:
Pageof 3
You have reached the last page of results.This site can display upto 29 results.
Clinical Genetics|May 23, 2006
Factors in decision making following genetic counseling for pre-natal diagnosis of de novo chromosomal rearrangementsR Wallerstein, V Strmen, J Durcan, et al.
Clinical Genetics|August 8, 2009
Copy number variations in three children with sudden infant deathG A Toruner, R Kurvathi, R Sugalski, et al.
Journal of Medical Genetics|March 1, 1997
Submicroscopic deletions at 16p13.3 in Rubinstein-Taybi syndrome: frequency and clinical manifestations in a North American populationR Wallerstein, C E Anderson, B Hay, et al.
American Journal of Medical Genetics|June 13, 1997
Lateral meningocele syndrome: three new patients and review of the literatureK W Gripp, C I Scott, H E Hughes, et al.
Clinical Genetics|September 7, 2016
Further evidence that de novo missense and truncating variants in ZBTB18 cause intellectual disability with variable featuresJ S Cohen, S Srivastava, K D Farwell Hagman, et al.
Proceedings of the National Academy of Sciences of the United States of America|April 25, 2002
Slowed conduction and ventricular tachycardia after targeted disruption of the cardiac sodium channel gene Scn5aG Alex Papadatos, Polly M R Wallerstein, Catherine E G Head, et al.
Journal of Medical Genetics|March 4, 2000
Diagnostic analysis of the Rubinstein-Taybi syndrome: five cosmids should be used for microdeletion detection and low number of protein truncating mutationsF Petrij, H G Dauwerse, R I Blough, et al.
American Journal of Human Genetics|May 20, 1999
The spectrum of mutations in TBX3: Genotype/Phenotype relationship in ulnar-mammary syndromeM Bamshad, T Le, W S Watkins, et al.
Prenatal Diagnosis|March 1, 2000
Common trisomy mosaicism diagnosed in amniocytes involving chromosomes 13, 18, 20 and 21: karyotype-phenotype correlationsR Wallerstein, M T Yu, R L Neu, et al.
Pageof 3