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Object |
contentType |
Journal Article|Research Support, Non-U.S. Gov't|Research Support, U.S. Gov't, Non-P.H.S.|Research Support, U.S. Gov't, P.H.S. |
endingPage |
6398 |
issn |
1091-6490 0027-8424 |
issueIdentifier |
14 |
pageRange |
6394-6398 |
publicationName |
Proceedings of the National Academy of Sciences of the United States of America |
startingPage |
6394 |
hasFundingAgency |
http://rdf.ncbi.nlm.nih.gov/pubchem/organization/MD5_e01b2377fafe8e7c7349c9fbe5f031a9 |
isSupportedBy |
http://rdf.ncbi.nlm.nih.gov/pubchem/grant/MD5_e32b3400e16f1935c9352a9761741df4 |
bibliographicCitation |
Rinchik EM, Carpenter DA, Handel MA. Pleiotropy in microdeletion syndromes: neurologic and spermatogenic abnormalities in mice homozygous for the p6H deletion are likely due to dysfunction of a single gene. Proc. Natl. Acad. Sci. U.S.A. 1995 Jul 03;92(14):6394–8. doi: 10.1073/pnas.92.14.6394. |
creator |
http://rdf.ncbi.nlm.nih.gov/pubchem/author/MD5_0fc358e0068d5bc6c708c2d831ff9f1f http://rdf.ncbi.nlm.nih.gov/pubchem/author/MD5_9d578067a07b870f25fca978428f7449 http://rdf.ncbi.nlm.nih.gov/pubchem/author/MD5_f017d6b1a69ffe0875fbcc510f5c6eae |
date |
1995-07-03-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
identifier |
https://doi.org/10.1073/pnas.92.14.6394 https://pubmed.ncbi.nlm.nih.gov/7604002 https://pubmed.ncbi.nlm.nih.gov/PMC41524 |
isPartOf |
https://portal.issn.org/resource/ISSN/0027-8424 http://rdf.ncbi.nlm.nih.gov/pubchem/journal/6653 https://portal.issn.org/resource/ISSN/1091-6490 |
language |
English |
source |
https://www.crossref.org/ https://pubmed.ncbi.nlm.nih.gov/ |
title |
Pleiotropy in microdeletion syndromes: neurologic and spermatogenic abnormalities in mice homozygous for the p6H deletion are likely due to dysfunction of a single gene. |
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