Showing results (311-320 of 869) with videos related to

Sort By:
Pageof 87
American Journal of Human Genetics|July 13, 2000
Identification of a novel gene on chromosome 7q31 that is interrupted by a translocation breakpoint in an autistic individualJ B Vincent, J A Herbrick, H M Gurling, et al.
American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics|January 19, 2020
Refining critical regions in 15q24 microdeletion syndrome pertaining to autismYi Liu, Yanqing Zhang, Mehdi Zarrei, et al.
American Journal of Medical Genetics. Part A|December 31, 2013
Clinical characteristics in patients with interstitial deletions of chromosome region 12q21-q22 and identification of a critical region associated with keratosis pilarisAlmundher Al-Maawali, Christian R Marshall, Stephen W Scherer, et al.
The Cochrane Database of Systematic Reviews|March 13, 2023
Medical interventions for traumatic hyphemaFasika A Woreta, Kristina B Lindsley, Almutez Gharaibeh, et al.
European Journal of Human Genetics : EJHG|February 23, 2026
Flexible and rapid validation of structural variation using adaptive samplingAida Paivandy, Felix Lenner, Jesper Eisfeldt, et al.
Contemporary Clinical Trials|February 4, 2021
National Institute of Mental Health Recruitment Monitoring Policy and Clinical Trial ImpactEugene I Kane, Gail L Daumit, Kevin M Fain, et al.
Genome Biology|April 19, 2003
Genome-wide detection of segmental duplications and potential assembly errors in the human genome sequenceJoseph Cheung, Xavier Estivill, Razi Khaja, et al.
Genomics|April 1, 1997
The XRCC2 DNA repair gene: identification of a positional candidateC E Tambini, A M George, J M Rommens, et al.
Pageof 87