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P Debeer

Showing results (11-20 of 16) with videos related to

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Clinical Genetics|November 15, 2002
Involvement of a palindromic chromosome 22-specific low-copy repeat in a constitutional t(X; 22)(q27;q11)P Debeer, R Mols, C Huysmans, et al.
European Journal of Human Genetics : EJHG|August 22, 2000
Physical map of a 1.5 mb region on 12p11.2 harbouring a synpolydactyly associated chromosomal breakpointP Debeer, E F Schoenmakers, R Thoelen, et al.
Journal of Medical Genetics|February 12, 2002
The fibulin-1 gene (FBLN1) is disrupted in a t(12;22) associated with a complex type of synpolydactylyP Debeer, E F P M Schoenmakers, W O Twal, et al.
Journal of Medical Genetics|July 9, 2009
Distal limb deficiencies, micrognathia syndrome, and syndromic forms of split hand foot malformation (SHFM) are caused by chromosome 10q genomic rearrangementsB I Dimitrov, T de Ravel, J Van Driessche, et al.
American Journal of Medical Genetics|September 20, 2001
Recurrent involvement of chromosomal region 6q21 in heterotaxyH Peeters, P Debeer, P Groenen, et al.
Human Genetics|February 28, 2003
PA26 is a candidate gene for heterotaxia in humans: identification of a novel PA26-related gene family in human and mouseH Peeters, P Debeer, A Bairoch, et al.
Pageof 2

Showing results (11-20 of 16) with videos related to

Sort By:
Pageof 2
You have reached the last page of results.This site can display upto 16 results.
Clinical Genetics|November 15, 2002
Involvement of a palindromic chromosome 22-specific low-copy repeat in a constitutional t(X; 22)(q27;q11)P Debeer, R Mols, C Huysmans, et al.
European Journal of Human Genetics : EJHG|August 22, 2000
Physical map of a 1.5 mb region on 12p11.2 harbouring a synpolydactyly associated chromosomal breakpointP Debeer, E F Schoenmakers, R Thoelen, et al.
Journal of Medical Genetics|February 12, 2002
The fibulin-1 gene (FBLN1) is disrupted in a t(12;22) associated with a complex type of synpolydactylyP Debeer, E F P M Schoenmakers, W O Twal, et al.
Journal of Medical Genetics|July 9, 2009
Distal limb deficiencies, micrognathia syndrome, and syndromic forms of split hand foot malformation (SHFM) are caused by chromosome 10q genomic rearrangementsB I Dimitrov, T de Ravel, J Van Driessche, et al.
American Journal of Medical Genetics|September 20, 2001
Recurrent involvement of chromosomal region 6q21 in heterotaxyH Peeters, P Debeer, P Groenen, et al.
Human Genetics|February 28, 2003
PA26 is a candidate gene for heterotaxia in humans: identification of a novel PA26-related gene family in human and mouseH Peeters, P Debeer, A Bairoch, et al.
Pageof 2