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B Penchaszadeh

Showing results (31-40 of 37) with videos related to

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Genetics and Molecular Biology|April 26, 2014
A tribute to josé maría ("chema") cantúVictor B Penchaszadeh, Augusto Rojas-Martinez, Adrián Llerena
American Journal of Medical Genetics|January 1, 1980
The IVIC syndrome: a new autosomal dominant complex pleiotropic syndrome with radial ray hypoplasia, hearing impairment, external ophthalmoplegia, and thrombocytopeniaS Arias, V B Penchaszadeh, J Pinto-Cisternas, et al.
American Journal of Medical Genetics|July 1, 1987
Interstitial deletion of chromosome 2 (p23p25)V B Penchaszadeh, P K Dowling, J G Davis, et al.
American Journal of Medical Genetics|November 1, 1987
Female external genitalia and müllerian duct derivatives in a 46,XY infant with the smith-lemli-Opitz syndromeM G Bialer, V B Penchaszadeh, E Kahn, et al.
American Journal of Medical Genetics|September 1, 1992
Double mosaic aneuploidy: 45,X/47,XY,+8 in a male infantB Schofield, A Babu, D Punales-Morejon, et al.
JAMA|November 17, 2001
Informed consent for population-based research involving geneticsL M Beskow, W Burke, J F Merz, et al.
Journal of Community Genetics|April 9, 2011
Community genetics. Its definition 2010Leo P Ten Kate, Lihadh Al-Gazali, Sonia Anand, et al.
Pageof 4

Showing results (31-40 of 37) with videos related to

Sort By:
Pageof 4
You have reached the last page of results.This site can display upto 37 results.
Genetics and Molecular Biology|April 26, 2014
A tribute to josé maría ("chema") cantúVictor B Penchaszadeh, Augusto Rojas-Martinez, Adrián Llerena
American Journal of Medical Genetics|January 1, 1980
The IVIC syndrome: a new autosomal dominant complex pleiotropic syndrome with radial ray hypoplasia, hearing impairment, external ophthalmoplegia, and thrombocytopeniaS Arias, V B Penchaszadeh, J Pinto-Cisternas, et al.
American Journal of Medical Genetics|July 1, 1987
Interstitial deletion of chromosome 2 (p23p25)V B Penchaszadeh, P K Dowling, J G Davis, et al.
American Journal of Medical Genetics|November 1, 1987
Female external genitalia and müllerian duct derivatives in a 46,XY infant with the smith-lemli-Opitz syndromeM G Bialer, V B Penchaszadeh, E Kahn, et al.
American Journal of Medical Genetics|September 1, 1992
Double mosaic aneuploidy: 45,X/47,XY,+8 in a male infantB Schofield, A Babu, D Punales-Morejon, et al.
JAMA|November 17, 2001
Informed consent for population-based research involving geneticsL M Beskow, W Burke, J F Merz, et al.
Journal of Community Genetics|April 9, 2011
Community genetics. Its definition 2010Leo P Ten Kate, Lihadh Al-Gazali, Sonia Anand, et al.
Pageof 4