Human Genome Epidemiology Literature Finder
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Records 1 - 5 (of 5 Records) |
| Query Trace: DLX5[original query] |
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| Autism and ultraconserved non-coding sequence on chromosome 7q. Psychiatric genetics 2006 1 16 (1): 19-23. Richler Esther, Reichert Jennifer G, Buxbaum Joseph D, McInnes Lynne Alis |
| Genetic analysis of vertebral trabecular bone density and cross-sectional area in older men. Osteoporosis international : a journal established as result of cooperation between the European Foundation for Osteoporosis and the National Osteoporosis Foundation of the USA 2011 Apr 22 (4): 1079-90. Zmuda J M, Yerges-Armstrong L M, Moffett S P, Klei L, Kammerer C M, Roeder K, Cauley J A, Kuipers A, Ensrud K E, Nestlerode C S, Hoffman A R, Lewis C E, Lang T F, Barrett-Connor E, Ferrell R E, Orwoll E S, |
| Deletions of exons with regulatory activity at the DYNC1I1 locus are associated with split-hand/split-foot malformation: array CGH screening of 134 unrelated families. Orphanet journal of rare diseases 2014 9 108. Tayebi Naeimeh, Jamsheer Aleksander, Flöttmann Ricarda, Sowinska-Seidler Anna, Doelken Sandra C, Oehl-Jaschkowitz Barbara, Hülsemann Wiebke, Habenicht Rolf, Klopocki Eva, Mundlos Stefan, Spielmann Mal |
| Transcriptional Changes following Cellular Knockdown of the Schizophrenia Risk Gene SETD1A Are Enriched for Common Variant Association with the Disorder. Molecular neuropsychiatry 2019 6 5 (2): 109-114. Cameron Darren, Blake Derek J, Bray Nicholas J, Hill Matthew |
| New pathogenic variant in DLX5: New clues for a clinical spectrum from split-hand-foot malformation to fibular aplasia, tibial campomelia and oligosyndactyly. Frontiers in genetics 2023 5 14 1165780. Anna Sifre-Ruiz, Amaia Sagasta, Erika Santos, Guiomar Perez de Nanclares, Karen E Hea |
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- Page last updated:Dec 01, 2023
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