Mapping of sudden infant death with dysgenesis of the testes syndrome (SIDDT) by a SNP genome scan and identification of TSPYL loss of function.

Puffenberger EG, Hu-Lince D, Parod JM, Craig DW, Dobrin SE, Conway AR, Donarum EA, Strauss KA, Dunckley T, Cardenas JF, Melmed KR, Wright CA, Liang W, Stafford P, Flynn CR, Morton DH, Stephan DA
Proc Natl Acad Sci U S A. 2004 101 (32): 11689-94

PMID: 15273283 · PMCID: PMC511011 · DOI:10.1073/pnas.0401194101

MeSH Terms (18)

Active Transport, Cell Nucleus Adult Chromosome Mapping DNA-Binding Proteins Family Health Female Frameshift Mutation Genome, Human Gonadal Dysgenesis Humans Infant Male Nuclear Proteins Nucleosomes Pedigree Sex-Determining Region Y Protein Sudden Infant Death Transcription Factors

Connections (1)

This publication is referenced by other Labnodes entities:

Links