Parents
Sign in to add mentorJudith Ann Brown | grad student | 1982 | VCU School of Medicine | |
(THE HUMAN NUCLEOLUS ORGANIZER REGION: A CYTOGENETIC, BIOCHEMICAL AND MOLECULAR GENETIC INVESTIGATION) |
BETA: Related publications
See more...
Publications
You can help our author matching system! If you notice any publications incorrectly attributed to this author, please sign in and mark matches as correct or incorrect. |
David D, Fino J, Oliveira R, et al. (2023) Balanced chromosomal rearrangements implicate YIPF5 and SPATC1L in non-obstructive oligoasthenozoospermia and oligozoospermia and of a derivative chromosome 22 in recurrent miscarriage. Gene. 147737 |
Srikanth S, Jain L, Zepeda-Mendoza C, et al. (2021) Position effects of 22q13 rearrangements on candidate genes in Phelan-McDermid syndrome. Plos One. 16: e0253859 |
Nalbandian K, Piña-Aguilar RE, Morton CC. (2020) Resolving Breakpoints of Chromosomal Rearrangements at the Nucleotide Level Using Sanger Sequencing. Current Protocols in Human Genetics. 108: e107 |
David D, Freixo JP, Fino J, et al. (2020) Comprehensive clinically oriented workflow for nucleotide level resolution and interpretation in prenatal diagnosis of de novo apparently balanced chromosomal translocations in their genomic landscape. Human Genetics |
Schilit SLP, Menon S, Friedrich C, et al. (2019) SYCP2 Translocation-Mediated Dysregulation and Frameshift Variants Cause Human Male Infertility. American Journal of Human Genetics |
Dong Z, Yan J, Xu F, et al. (2019) Genome Sequencing Explores Complexity of Chromosomal Abnormalities in Recurrent Miscarriage. American Journal of Human Genetics |
Wang H, Dong Z, Zhang R, et al. (2019) Low-pass genome sequencing versus chromosomal microarray analysis: implementation in prenatal diagnosis. Genetics in Medicine : Official Journal of the American College of Medical Genetics |
Wilch ES, Morton CC. (2018) Historical and Clinical Perspectives on Chromosomal Translocations. Advances in Experimental Medicine and Biology. 1044: 1-14 |
Waggoner D, Wain KE, Dubuc AM, et al. (2018) Yield of additional genetic testing after chromosomal microarray for diagnosis of neurodevelopmental disability and congenital anomalies: a clinical practice resource of the American College of Medical Genetics and Genomics (ACMG). Genetics in Medicine : Official Journal of the American College of Medical Genetics |
Dong Z, Ye L, Yang Z, et al. (2018) Balanced Chromosomal Rearrangement Detection by Low-Pass Whole-Genome Sequencing. Current Protocols in Human Genetics. 96: 8.18.1-8.18.16 |