Search research articles
Contact Us
Filters
Showing results (171-180 of 173) with videos related to
Page
of 18
Sort By:
You have reached the last page of results.
This site can display upto 173 results.
American Journal of Human Genetics
|
February 1, 2023
Bi-allelic TTI1 variants cause an autosomal-recessive neurodevelopmental disorder with microcephaly
Margaux Serey-Gaut, Marisol Cortes, Periklis Makrythanasis, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics
|
January 15, 2019
TBX6-associated congenital scoliosis (TACS) as a clinically distinguishable subtype of congenital scoliosis: further evidence supporting the compound inheritance and TBX6 gene dosage model
Jiaqi Liu, Nan Wu, , et al.
American Journal of Human Genetics
|
March 5, 2019
Missense Variants in the Histone Acetyltransferase Complex Component Gene TRRAP Cause Autism and Syndromic Intellectual Disability
Benjamin Cogné, Sophie Ehresmann, Eliane Beauregard-Lacroix, et al.
Page
of 18
Search research articles
Search
Showing results (171-180 of 173) with videos related to
Sort By:
Page
of 18
You have reached the last page of results.
This site can display upto 173 results.
American Journal of Human Genetics
|
February 1, 2023
Bi-allelic TTI1 variants cause an autosomal-recessive neurodevelopmental disorder with microcephaly
Margaux Serey-Gaut, Marisol Cortes, Periklis Makrythanasis, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics
|
January 15, 2019
TBX6-associated congenital scoliosis (TACS) as a clinically distinguishable subtype of congenital scoliosis: further evidence supporting the compound inheritance and TBX6 gene dosage model
Jiaqi Liu, Nan Wu, , et al.
American Journal of Human Genetics
|
March 5, 2019
Missense Variants in the Histone Acetyltransferase Complex Component Gene TRRAP Cause Autism and Syndromic Intellectual Disability
Benjamin Cogné, Sophie Ehresmann, Eliane Beauregard-Lacroix, et al.
Page
of 18