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Year | Number of Results |
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2004 | 1 |
2006 | 2 |
2024 | 0 |
PubMed for id: 463019
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Mutations in the lipoma HMGIC fusion partner-like 5 (LHFPL5) gene cause autosomal recessive nonsyndromic hearing loss.
Hum Mutat. 2006 Jul;27(7):633-9. doi: 10.1002/humu.20368.
Hum Mutat. 2006.
PMID: 16752389
Molecular genetic analysis of a de novo balanced translocation t(6;17)(p21.31;q11.2) associated with hypospadias and anorectal malformation.
Mansouri MR, Carlsson B, Davey E, Nordenskjöld A, Wester T, Annerén G, Läckgren G, Dahl N.
Mansouri MR, et al.
Hum Genet. 2006 Mar;119(1-2):162-8. doi: 10.1007/s00439-005-0122-9. Epub 2006 Jan 3.
Hum Genet. 2006.
PMID: 16395596
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Isolation, tissue distribution and prokaryotic expression of a novel human X-linked gene LHFPL1.
Huang C, Guo J, Liu S, Shan Y, Wu S, Cai Y, Yu L.
Huang C, et al.
DNA Seq. 2004 Aug;15(4):299-302. doi: 10.1080/10425170412331279620.
DNA Seq. 2004.
PMID: 15620218
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