Human Genome Epidemiology Literature Finder
Records 1 - 3 (of 3 Records) |
Query Trace: Syndrome and TSPYL1[original query] |
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Genetic investigation of the TSPYL1 gene in sudden infant death syndrome. Genetics in medicine : official journal of the American College of Medical Genetics 2006 Jan 8 (1): 55-8. Hering Robert, Frade-Martinez Rosario, Bajanowski Thomas, Poets Christian F, Tschentscher Frank, Riess Ol |
Should TSPYL1 mutation screening be included in routine diagnostics of male idiopathic infertility? Fertility and sterility 2012 Feb 97 (2): 402-6. Javaher Poupak, Stuhrmann Manfred, Wilke Christina, Frenzel Eileen, Manukjan Georgi, Grosshenig Anika, Dechend Frank, Schwaab Eva, Schmidtke Jörg, Schubert Stephan |
Variants in TSPYL1 are not associated with sudden infant death syndrome in a cohort of deceased infants from Switzerland. Molecular and cellular probes 2015 Feb 29 (1): 31-4. Schubert Stephanie, Haas Cordula, Bartsch Christine, Mirshekarnejad Mandana, Kohrs Sarah, Roettinger Irene, Grosshennig Anika, Stuhrmann Manfred, Scholz Caroline, Schmidtke Jö |
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