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Table representation of search results timeline featuring number of search results per year.
Year | Number of Results |
---|---|
1997 | 1 |
1999 | 1 |
2001 | 1 |
2002 | 1 |
2003 | 1 |
2024 | 0 |
PubMed (OMIM) for id: 350211
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Page 1
CATSPER2, a human autosomal nonsyndromic male infertility gene.
Eur J Hum Genet. 2003 Jul;11(7):497-502. doi: 10.1038/sj.ejhg.5200991.
Eur J Hum Genet. 2003.
PMID: 12825070
Congenital dyserythropoietic anemia type I is caused by mutations in codanin-1.
Dgany O, Avidan N, Delaunay J, Krasnov T, Shalmon L, Shalev H, Eidelitz-Markus T, Kapelushnik J, Cattan D, Pariente A, Tulliez M, Crétien A, Schischmanoff PO, Iolascon A, Fibach E, Koren A, Rössler J, Le Merrer M, Yaniv I, Zaizov R, Ben-Asher E, Olender T, Lancet D, Beckmann JS, Tamary H.
Dgany O, et al.
Am J Hum Genet. 2002 Dec;71(6):1467-74. doi: 10.1086/344781. Epub 2002 Nov 14.
Am J Hum Genet. 2002.
PMID: 12434312
Free PMC article.
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Mutations in a new gene encoding a protein of the hair bundle cause non-syndromic deafness at the DFNB16 locus.
Verpy E, Masmoudi S, Zwaenepoel I, Leibovici M, Hutchin TP, Del Castillo I, Nouaille S, Blanchard S, Lainé S, Popot JL, Moreno F, Mueller RF, Petit C.
Verpy E, et al.
Nat Genet. 2001 Nov;29(3):345-9. doi: 10.1038/ng726.
Nat Genet. 2001.
PMID: 11687802
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Deafness locus DFNB16 is located on chromosome 15q13-q21 within a 5-cM interval flanked by markers D15S994 and D15S132.
Villamar M, del Castillo I, Valle N, Romero L, Moreno F.
Villamar M, et al.
Am J Hum Genet. 1999 Apr;64(4):1238-41. doi: 10.1086/302321.
Am J Hum Genet. 1999.
PMID: 10090914
Free PMC article.
No abstract available.
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A new locus for non-syndromal, autosomal recessive, sensorineural hearing loss (DFNB16) maps to human chromosome 15q21-q22.
Campbell DA, McHale DP, Brown KA, Moynihan LM, Houseman M, Karbani G, Parry G, Janjua AH, Newton V, al-Gazali L, Markham AF, Lench NJ, Mueller RF.
Campbell DA, et al.
J Med Genet. 1997 Dec;34(12):1015-7. doi: 10.1136/jmg.34.12.1015.
J Med Genet. 1997.
PMID: 9429146
Free PMC article.
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