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Showing results (71-80 of 76) with videos related to

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Journal of Medical Genetics|April 5, 2003
The imprinted region on human chromosome 7q32 extends to the carboxypeptidase A gene cluster: an imprinted candidate for Silver-Russell syndromeL Bentley, K Nakabayashi, D Monk, et al.
Journal of Dental Research|March 28, 2019
Disruption of FOXF2 as a Likely Cause of Absent Uvula in an Egyptian FamilyR Seselgyte, D Bryant, C Demetriou, et al.
Journal of Medical Genetics|January 20, 2004
TBX22 mutations are a frequent cause of cleft palateA C B Marçano, K Doudney, C Braybrook, et al.
American Journal of Human Genetics|February 15, 2001
Conflicting reports of imprinting status of human GRB10 in developing brain: how reliable are somatic cell hybrids for predicting allelic origin of expression?S Mergenthaler, M P Hitchins, N Blagitko-Dorfs, et al.
Journal of Medical Genetics|August 3, 2004
Genomic imprinting of PPP1R9A encoding neurabin I in skeletal muscle and extra-embryonic tissuesK Nakabayashi, S Makino, S Minagawa, et al.
Clinical Genetics|June 29, 2016
Impact of rare variants in ARHGAP29 to the etiology of oral clefts: role of loss-of-function vs missense variantsC P Savastano, L A Brito, Á C Faria, et al.
Pageof 8

Showing results (71-80 of 76) with videos related to

Sort By:
Pageof 8
You have reached the last page of results.This site can display upto 76 results.
Journal of Medical Genetics|April 5, 2003
The imprinted region on human chromosome 7q32 extends to the carboxypeptidase A gene cluster: an imprinted candidate for Silver-Russell syndromeL Bentley, K Nakabayashi, D Monk, et al.
Journal of Dental Research|March 28, 2019
Disruption of FOXF2 as a Likely Cause of Absent Uvula in an Egyptian FamilyR Seselgyte, D Bryant, C Demetriou, et al.
Journal of Medical Genetics|January 20, 2004
TBX22 mutations are a frequent cause of cleft palateA C B Marçano, K Doudney, C Braybrook, et al.
American Journal of Human Genetics|February 15, 2001
Conflicting reports of imprinting status of human GRB10 in developing brain: how reliable are somatic cell hybrids for predicting allelic origin of expression?S Mergenthaler, M P Hitchins, N Blagitko-Dorfs, et al.
Journal of Medical Genetics|August 3, 2004
Genomic imprinting of PPP1R9A encoding neurabin I in skeletal muscle and extra-embryonic tissuesK Nakabayashi, S Makino, S Minagawa, et al.
Clinical Genetics|June 29, 2016
Impact of rare variants in ARHGAP29 to the etiology of oral clefts: role of loss-of-function vs missense variantsC P Savastano, L A Brito, Á C Faria, et al.
Pageof 8