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M Bamshad

Showing results (21-30 of 47) with videos related to

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American Journal of Medical Genetics. Part A|November 15, 2006
A new distal arthrogryposis syndrome characterized by plantar flexion contracturesD A Stevenson, K J Swoboda, R K Sanders, et al.
American Journal of Human Genetics|March 7, 1998
Syndromic ectrodactyly with severe limb, ectodermal, urogenital, and palatal defects maps to chromosome 19J R O'Quinn, R C Hennekam, L B Jorde, et al.
The American Journal of Physiology|August 5, 1998
Central nervous system origins of the sympathetic nervous system outflow to white adipose tissueM Bamshad, V T Aoki, M G Adkison, et al.
Genetics|April 30, 1998
Signatures of population expansion in microsatellite repeat dataM Kimmel, R Chakraborty, J P King, et al.
Human Molecular Genetics|October 1, 1995
A gene for ulnar-mammary syndrome maps to 12q23-q24.1M Bamshad, P A Krakowiak, W S Watkins, et al.
Clinical Genetics|December 8, 2016
Mutations in DYNC2H1, the cytoplasmic dynein 2, heavy chain 1 motor protein gene, cause short-rib polydactyly type I, Saldino-Noonan typeN Badiner, S P Taylor, K Forlenza, et al.
Proceedings of the National Academy of Sciences of the United States of America|April 1, 1997
Microsatellite diversity and the demographic history of modern humansL B Jorde, A R Rogers, M Bamshad, et al.
American Journal of Human Genetics|February 1, 1997
A variant of Freeman-Sheldon syndrome maps to 11p15.5-pterP A Krakowiak, J R O'Quinn, J F Bohnsack, et al.
Human Biology|February 1, 1996
mtDNA variation in caste populations of Andhra Pradesh, IndiaM Bamshad, A E Fraley, M H Crawford, et al.
Pediatric Research|March 24, 1999
Reconstructing the history of human limb development: lessons from birth defectsM Bamshad, W S Watkins, M E Dixon, et al.
Pageof 5

Showing results (21-30 of 47) with videos related to

Sort By:
Pageof 5
American Journal of Medical Genetics. Part A|November 15, 2006
A new distal arthrogryposis syndrome characterized by plantar flexion contracturesD A Stevenson, K J Swoboda, R K Sanders, et al.
American Journal of Human Genetics|March 7, 1998
Syndromic ectrodactyly with severe limb, ectodermal, urogenital, and palatal defects maps to chromosome 19J R O'Quinn, R C Hennekam, L B Jorde, et al.
The American Journal of Physiology|August 5, 1998
Central nervous system origins of the sympathetic nervous system outflow to white adipose tissueM Bamshad, V T Aoki, M G Adkison, et al.
Genetics|April 30, 1998
Signatures of population expansion in microsatellite repeat dataM Kimmel, R Chakraborty, J P King, et al.
Human Molecular Genetics|October 1, 1995
A gene for ulnar-mammary syndrome maps to 12q23-q24.1M Bamshad, P A Krakowiak, W S Watkins, et al.
Clinical Genetics|December 8, 2016
Mutations in DYNC2H1, the cytoplasmic dynein 2, heavy chain 1 motor protein gene, cause short-rib polydactyly type I, Saldino-Noonan typeN Badiner, S P Taylor, K Forlenza, et al.
Proceedings of the National Academy of Sciences of the United States of America|April 1, 1997
Microsatellite diversity and the demographic history of modern humansL B Jorde, A R Rogers, M Bamshad, et al.
American Journal of Human Genetics|February 1, 1997
A variant of Freeman-Sheldon syndrome maps to 11p15.5-pterP A Krakowiak, J R O'Quinn, J F Bohnsack, et al.
Human Biology|February 1, 1996
mtDNA variation in caste populations of Andhra Pradesh, IndiaM Bamshad, A E Fraley, M H Crawford, et al.
Pediatric Research|March 24, 1999
Reconstructing the history of human limb development: lessons from birth defectsM Bamshad, W S Watkins, M E Dixon, et al.
Pageof 5