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Year | Number of Results |
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2002 | 1 |
2003 | 1 |
2006 | 1 |
2018 | 1 |
2024 | 0 |
PubMed (OMIM) for id: 150365
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Causative Mutations and Mechanism of Androgenetic Hydatidiform Moles.
Am J Hum Genet. 2018 Nov 1;103(5):740-751. doi: 10.1016/j.ajhg.2018.10.007.
Am J Hum Genet. 2018.
PMID: 30388401
Free PMC article.
Polymorphic alleles of the human MEI1 gene are associated with human azoospermia by meiotic arrest.
Sato H, Miyamoto T, Yogev L, Namiki M, Koh E, Hayashi H, Sasaki Y, Ishikawa M, Lamb DJ, Matsumoto N, Birk OS, Niikawa N, Sengoku K.
Sato H, et al.
J Hum Genet. 2006;51(6):533-540. doi: 10.1007/s10038-006-0394-5. Epub 2006 May 9.
J Hum Genet. 2006.
PMID: 16683055
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Positional cloning and characterization of Mei1, a vertebrate-specific gene required for normal meiotic chromosome synapsis in mice.
Libby BJ, Reinholdt LG, Schimenti JC.
Libby BJ, et al.
Proc Natl Acad Sci U S A. 2003 Dec 23;100(26):15706-11. doi: 10.1073/pnas.2432067100. Epub 2003 Dec 10.
Proc Natl Acad Sci U S A. 2003.
PMID: 14668445
Free PMC article.
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The mouse meiotic mutation mei1 disrupts chromosome synapsis with sexually dimorphic consequences for meiotic progression.
Libby BJ, De La Fuente R, O'Brien MJ, Wigglesworth K, Cobb J, Inselman A, Eaker S, Handel MA, Eppig JJ, Schimenti JC.
Libby BJ, et al.
Dev Biol. 2002 Feb 15;242(2):174-87. doi: 10.1006/dbio.2001.0535.
Dev Biol. 2002.
PMID: 11820814
Free article.
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