E W Jabs - JoVE Visualize

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American Journal of Human Genetics|August 1, 1995

Analysis of phenotypic features and FGFR2 mutations in Apert syndromeW J Park, C Theda, N E Maestri, et al.

Proceedings of the National Academy of Sciences of the United States of America|June 13, 2006

Advancing age has differential effects on DNA damage, chromatin integrity, gene mutations, and aneuploidies in spermA J Wyrobek, B Eskenazi, S Young, et al.

Genomics|October 1, 1993

Genetic and physical mapping of the Treacher Collins syndrome locus with respect to loci in the chromosome 5q3 regionE W Jabs, X Li, M Lovett, et al.

Genomics|September 15, 1994

Human and mouse chromosomal mapping of the myeloid cell leukemia-1 gene: MCL1 maps to human chromosome 1q21, a region that is frequently altered in preneoplastic and neoplastic diseaseR W Craig, E W Jabs, P Zhou, et al.

Public Health Genomics|December 14, 2012

Genetic and lifestyle causal beliefs about obesity and associated diseases among ethnically diverse patients: a structured interview studyS C Sanderson, M A Diefenbach, S A Streicher, et al.

Genomics|September 1, 1992

Assignment of genes encoding a unique cytokine (IL12) composed of two unrelated subunits to chromosomes 3 and 5D Sieburth, E W Jabs, J A Warrington, et al.

Ultrasound in Obstetrics & Gynecology : the Official Journal of the International Society of Ultrasound in Obstetrics and Gynecology|February 5, 2000

Second-trimester molecular prenatal diagnosis of sporadic Apert syndrome following suspicious ultrasound findingsJ C Ferreira, S M Carter, P S Bernstein, et al.

Biological Psychiatry|April 21, 2001

Regional cortical white matter reductions in velocardiofacial syndrome: a volumetric MRI analysisW R Kates, C P Burnette, E W Jabs, et al.

Cell|November 5, 1993

A mutation in the homeodomain of the human MSX2 gene in a family affected with autosomal dominant craniosynostosisE W Jabs, U Müller, X Li, et al.

American Journal of Medical Genetics|October 1, 1993

Saethre-Chotzen syndrome with familial translocation at chromosome 7p22C S Reid, L E McMorrow, D M McDonald-McGinn, et al.

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Showing results (61-70 of 103) with videos related to

Sort By:

Pageof 11

American Journal of Human Genetics|August 1, 1995

Analysis of phenotypic features and FGFR2 mutations in Apert syndromeW J Park, C Theda, N E Maestri, et al.

Proceedings of the National Academy of Sciences of the United States of America|June 13, 2006

Advancing age has differential effects on DNA damage, chromatin integrity, gene mutations, and aneuploidies in spermA J Wyrobek, B Eskenazi, S Young, et al.

Genomics|October 1, 1993

Genetic and physical mapping of the Treacher Collins syndrome locus with respect to loci in the chromosome 5q3 regionE W Jabs, X Li, M Lovett, et al.

Genomics|September 15, 1994

Human and mouse chromosomal mapping of the myeloid cell leukemia-1 gene: MCL1 maps to human chromosome 1q21, a region that is frequently altered in preneoplastic and neoplastic diseaseR W Craig, E W Jabs, P Zhou, et al.

Public Health Genomics|December 14, 2012

Genetic and lifestyle causal beliefs about obesity and associated diseases among ethnically diverse patients: a structured interview studyS C Sanderson, M A Diefenbach, S A Streicher, et al.

Genomics|September 1, 1992

Assignment of genes encoding a unique cytokine (IL12) composed of two unrelated subunits to chromosomes 3 and 5D Sieburth, E W Jabs, J A Warrington, et al.

Ultrasound in Obstetrics & Gynecology : the Official Journal of the International Society of Ultrasound in Obstetrics and Gynecology|February 5, 2000

Second-trimester molecular prenatal diagnosis of sporadic Apert syndrome following suspicious ultrasound findingsJ C Ferreira, S M Carter, P S Bernstein, et al.

Biological Psychiatry|April 21, 2001

Regional cortical white matter reductions in velocardiofacial syndrome: a volumetric MRI analysisW R Kates, C P Burnette, E W Jabs, et al.

Cell|November 5, 1993

A mutation in the homeodomain of the human MSX2 gene in a family affected with autosomal dominant craniosynostosisE W Jabs, U Müller, X Li, et al.

American Journal of Medical Genetics|October 1, 1993

Saethre-Chotzen syndrome with familial translocation at chromosome 7p22C S Reid, L E McMorrow, D M McDonald-McGinn, et al.

Pageof 11