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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 syndrome
L 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 Family
R Seselgyte, D Bryant, C Demetriou, et al.
Journal of Medical Genetics
|
January 20, 2004
TBX22 mutations are a frequent cause of cleft palate
A 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 tissues
K 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 variants
C P Savastano, L A Brito, Á C Faria, et al.
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of 8
Search research articles
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Showing results (71-80 of 76) with videos related to
Sort By:
Page
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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 syndrome
L 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 Family
R Seselgyte, D Bryant, C Demetriou, et al.
Journal of Medical Genetics
|
January 20, 2004
TBX22 mutations are a frequent cause of cleft palate
A 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 tissues
K 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 variants
C P Savastano, L A Brito, Á C Faria, et al.
Page
of 8