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American Journal of Medical Genetics. Part C, Seminars in Medical Genetics|July 14, 2012
Mutation-based growth charts for SEDC and other COL2A1 related dysplasiasPaulien A Terhal, Paula van Dommelen, Martine Le Merrer, et al.
American Journal of Human Genetics|May 20, 2005
Genetic variation in the human androgen receptor gene is the major determinant of common early-onset androgenetic alopeciaAxel M Hillmer, Sandra Hanneken, Sibylle Ritzmann, et al.
American Journal of Human Genetics|August 2, 2016
Exome Sequencing Identifies Biallelic MSH3 Germline Mutations as a Recessive Subtype of Colorectal Adenomatous PolyposisRonja Adam, Isabel Spier, Bixiao Zhao, et al.
The Journal of Allergy and Clinical Immunology|May 27, 2026
Multi-cytokine based TWAS for seven inflammatory skin disorders identify candidate causal genes in keratinocytesHaihan Zhang, Matthew T Patrick, Mrinal K Sarkar, et al.
The British Journal of Dermatology|September 6, 2023
Short anagen hair syndrome: association with mono- and biallelic variants in WNT10A and a genetic overlap with male pattern hair lossNicole Cesarato, Agnes Schwieger-Briel, Yasmina Gossmann, et al.
The Journal of Investigative Dermatology|January 30, 2013
Androgenetic alopecia: identification of four genetic risk loci and evidence for the contribution of WNT signaling to its etiologyStefanie Heilmann, Amy K Kiefer, Nadine Fricker, et al.
Nature Genetics|October 14, 2008
Susceptibility variants for male-pattern baldness on chromosome 20p11Axel M Hillmer, Felix F Brockschmidt, Sandra Hanneken, et al.
American Journal of Human Genetics|June 5, 2020
Mutations in SREBF1, Encoding Sterol Regulatory Element Binding Transcription Factor 1, Cause Autosomal-Dominant IFAP SyndromeHuijun Wang, Aytaj Humbatova, Yuanxiang Liu, et al.
Genes|January 13, 2021
Meta-Analysis of Mutations in ALOX12B or ALOXE3 Identified in a Large Cohort of 224 PatientsAlrun Hotz, Julia Kopp, Emmanuelle Bourrat, et al.
European Journal of Human Genetics : EJHG|October 27, 2011
Genome-wide pooling approach identifies SPATA5 as a new susceptibility locus for alopecia areataLina M Forstbauer, Felix F Brockschmidt, Valentina Moskvina, et al.
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