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European Journal of Medical Genetics|October 5, 2010
Long-term outcomes of adults with features of VACTERL associationManu S Raam, Daniel E Pineda-Alvarez, Donald W Hadley, et al.
Molecular Syndromology|May 20, 2016
X-Linked Candidate Genes for a Ciliopathy-Like DisorderAshleigh R Pavey, Thierry Vilboux, Holly E Babcock, et al.
HGG Advances|January 20, 2022
Neural network classifiers for images of genetic conditions with cutaneous manifestationsDat Duong, Rebekah L Waikel, Ping Hu, et al.
Birth Defects Research|September 20, 2018
Clinical epidemiology of congenital heart disease in Nigerian children, 2012-2017Ekanem N Ekure, Nnenna Kalu, Ogochukwu J Sokunbi, et al.
Birth Defects Research. Part A, Clinical and Molecular Teratology|August 1, 2012
Comparison of mutation findings in ZIC2 between microform and classical holoprosencephaly in a Brazilian cohortLucilene A Ribeiro, Erich Roessler, Ping Hu, et al.
American Journal of Human Genetics|April 23, 2019
A CCR4-NOT Transcription Complex, Subunit 1, CNOT1, Variant Associated with HoloprosencephalyPaul Kruszka, Seth I Berger, Karin Weiss, et al.
Proceedings of the National Academy of Sciences of the United States of America|January 20, 2011
Neuropilin-1 attenuates autoreactivity in experimental autoimmune encephalomyelitisBenjamin D Solomon, Cynthia Mueller, Wook-Jin Chae, et al.
Medrxiv : the Preprint Server for Health Sciences|June 9, 2020
The Role of Host Genetic Factors in Coronavirus Susceptibility: Review of Animal and Systematic Review of Human LiteratureMarissa LoPresti, David B Beck, Priya Duggal, et al.
American Journal of Medical Genetics. Part A|October 6, 2018
Basan gets a new fingerprint: Mutations in the skin-specific isoform of SMARCAD1 cause ectodermal dysplasia syndromes with adermatoglyphiaMonica N Valentin, Benjamin D Solomon, Gabriele Richard, et al.
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