V C Sheffield - JoVE Visualize

Search research articles

ABOUT JoVE

Overview Leadership Blog JoVE Help Center

AUTHORS

Publishing Process Editorial Board Scope & Policies Peer Review FAQ Submit

LIBRARIANS

Testimonials Subscriptions Access Resources Library Advisory Board FAQ

RESEARCH

JoVE Journal Methods Collections JoVE Encyclopedia of Experiments Archive

EDUCATION

JoVE Core JoVE Business JoVE Science Education JoVE Lab Manual Faculty Resource Center Faculty Site

Terms & Conditions of Use

Policies

Search research articles

ABOUT JoVE

Overview Leadership Blog JoVE Help Center

AUTHORS

Publishing Process Editorial Board Scope & Policies Peer Review FAQ Submit

LIBRARIANS

Testimonials Subscriptions Access Resources Library Advisory Board FAQ

RESEARCH

JoVE Journal Methods Collections JoVE Encyclopedia of Experiments Archive

EDUCATION

JoVE Core JoVE Business JoVE Science Education JoVE Lab Manual Faculty Resource Center Faculty Site

Terms & Conditions of Use

Policies

Filters

V C Sheffield

Showing results (101-110 of 153) with videos related to

Pageof 16

Sort By:

Genome Research|July 13, 1999

The CMT2D locus: refined genetic position and construction of a bacterial clone-based physical mapR E Ellsworth, V Ionasescu, C Searby, et al.

Human Mutation|April 24, 2001

Pendred syndrome, DFNB4, and PDS/SLC26A4 identification of eight novel mutations and possible genotype-phenotype correlationsC Campbell, R A Cucci, S Prasad, et al.

Nature Genetics|December 1, 1993

Linkage of Bardet-Biedl syndrome to chromosome 16q and evidence for non-allelic genetic heterogeneityA E Kwitek-Black, R Carmi, G M Duyk, et al.

Human Molecular Genetics|January 1, 1997

Identification of a complex congenital heart defect susceptibility locus by using DNA pooling and shared segment analysisV C Sheffield, M E Pierpont, D Nishimura, et al.

Proceedings of the National Academy of Sciences of the United States of America|October 15, 1992

Low frequency of p53 mutations observed in a diverse collection of primary hepatocellular carcinomasK H Buetow, V C Sheffield, M Zhu, et al.

Bioinformatics (Oxford, England)|September 10, 2002

Pooled library tissue tags for EST-based gene discoveryA J Gavin, T E Scheetz, C A Roberts, et al.

Science (New York, N.Y.)|September 30, 1994

A comprehensive human linkage map with centimorgan density. Cooperative Human Linkage Center (CHLC)J C Murray, K H Buetow, J L Weber, et al.

Human Molecular Genetics|August 1, 1995

Linkage of autosomal dominant iris hypoplasia to the region of the Rieger syndrome locus (4q25)E Héon, B P Sheth, J W Kalenak, et al.

Science (New York, N.Y.)|September 30, 1994

Human genetic map. Genome maps V. Wall chartK H Buetow, S Ludwigsen, T Scherpbier-Heddema, et al.

Developmental Dynamics : an Official Publication of the American Association of Anatomists|September 4, 1999

Expression of the Mf1 gene in developing mouse hearts: implication in the development of human congenital heart defectsR E Swiderski, R S Reiter, D Y Nishimura, et al.

Pageof 16

Search research articles

Showing results (101-110 of 153) with videos related to

Sort By:

Pageof 16

Genome Research|July 13, 1999

The CMT2D locus: refined genetic position and construction of a bacterial clone-based physical mapR E Ellsworth, V Ionasescu, C Searby, et al.

Human Mutation|April 24, 2001

Pendred syndrome, DFNB4, and PDS/SLC26A4 identification of eight novel mutations and possible genotype-phenotype correlationsC Campbell, R A Cucci, S Prasad, et al.

Nature Genetics|December 1, 1993

Linkage of Bardet-Biedl syndrome to chromosome 16q and evidence for non-allelic genetic heterogeneityA E Kwitek-Black, R Carmi, G M Duyk, et al.

Human Molecular Genetics|January 1, 1997

Identification of a complex congenital heart defect susceptibility locus by using DNA pooling and shared segment analysisV C Sheffield, M E Pierpont, D Nishimura, et al.

Proceedings of the National Academy of Sciences of the United States of America|October 15, 1992

Low frequency of p53 mutations observed in a diverse collection of primary hepatocellular carcinomasK H Buetow, V C Sheffield, M Zhu, et al.

Bioinformatics (Oxford, England)|September 10, 2002

Pooled library tissue tags for EST-based gene discoveryA J Gavin, T E Scheetz, C A Roberts, et al.

Science (New York, N.Y.)|September 30, 1994

A comprehensive human linkage map with centimorgan density. Cooperative Human Linkage Center (CHLC)J C Murray, K H Buetow, J L Weber, et al.

Human Molecular Genetics|August 1, 1995

Linkage of autosomal dominant iris hypoplasia to the region of the Rieger syndrome locus (4q25)E Héon, B P Sheth, J W Kalenak, et al.

Science (New York, N.Y.)|September 30, 1994

Human genetic map. Genome maps V. Wall chartK H Buetow, S Ludwigsen, T Scherpbier-Heddema, et al.

Developmental Dynamics : an Official Publication of the American Association of Anatomists|September 4, 1999

Expression of the Mf1 gene in developing mouse hearts: implication in the development of human congenital heart defectsR E Swiderski, R S Reiter, D Y Nishimura, et al.

Pageof 16