Andrew R. Zinn
Affiliations: | McDermott Center for Human Growth and Development | University of Texas Southwestern Medical Center, Dallas, TX, United States |
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"Andrew Zinn"
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| Starokadomskyy P, Wilton KM, Krzewski K, et al. (2019) NK cell defects in X-linked pigmentary reticulate disorder. Jci Insight. 4 |
| Ross JL, Bloy L, Roberts TPL, et al. (2019) Y chromosome gene copy number and lack of autism phenotype in a male with an isodicentric Y chromosome and absent NLGN4Y expression. American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics |
| Raznahan A, Parikshak NN, Chandran V, et al. (2018) Sex-chromosome dosage effects on gene expression in humans. Proceedings of the National Academy of Sciences of the United States of America |
| Starokadomskyy P, Sifuentes-Dominguez L, Gemelli T, et al. (2017) Evolution of the skin manifestations of X-linked Pigmentary Reticulate Disorder. The British Journal of Dermatology |
| Benito-Sanz S, Belinchon-Martínez A, Aza-Carmona M, et al. (2016) Identification of 15 novel partial SHOX deletions and 13 partial duplications, and a review of the literature reveals intron 3 to be a hotspot region. Journal of Human Genetics |
| Ross JL, Tartaglia N, Merry DE, et al. (2015) Behavioral phenotypes in males with XYY and possible role of increased NLGN4Y expression in autism features. Genes, Brain, and Behavior. 14: 137-44 |
| Harrison SM, Campbell IM, Keays M, et al. (2013) Screening and familial characterization of copy-number variations in NR5A1 in 46,XY disorders of sex development and premature ovarian failure. American Journal of Medical Genetics. Part A. 161: 2487-94 |
| Payne AR, Chang SW, Koenig SN, et al. (2012) Submicroscopic chromosomal copy number variations identified in children with hypoplastic left heart syndrome. Pediatric Cardiology. 33: 757-63 |
| Bhoj EJ, Ramos P, Baker LA, et al. (2012) Erratum: Human balanced translocation and mouse gene inactivation implicate Basonuclin 2 in distal urethral development (European Journal of Human Genetics (2011) DOI: 10.1038/ejhg.2010.245) European Journal of Human Genetics. 20 |
| Bhoj EJ, Ramos P, Baker LA, et al. (2011) Human balanced translocation and mouse gene inactivation implicate Basonuclin 2 in distal urethral development. European Journal of Human Genetics : Ejhg. 19: 540-6 |