Chromosome 1p36 Deletions: The Clinical Phenotype and Molecular Characterization of a Common Newly Delineated Syndrome (Q34743172)
scientific article published on September 1, 1997
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(P304) 642-650
(P407) (Q1860)
(P433) 3
(P478) 61
(P577) Monday, September 1, 1997
Monday, September 1, 1997
(P921) (Q104053)
(Q16918398)
(P953) https://doi.org/10.1086/515520
https://europepmc.org/articles/PMC1715949
https://europepmc.org/articles/PMC1715949?pdf=render
https://api.elsevier.com/content/article/PII:S0002929707643286?httpAccept=text/xml
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(P1433) (Q4744249)
(P1476) "Chromosome 1p36 deletions: the clinical phenotype and molecular characterization of a common newly delineated syndrome" (language: en)
"Chromosome 1p36 Deletions: The Clinical Phenotype and Molecular Characterization of a Common Newly Delineated Syndrome" (language: en)
(P2093) S. K. Shapira
C. McCaskill
H. Northrup
A. S. Spikes
F. F. Elder
V. R. Sutton
J. R. Korenberg
F. Greenberg
L. G. Shaffer
(P2860) (Q34256123)
(Q41928115)
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(Q35644261)
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(Q33858951)
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(Q36283158)
(Q24563904)
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(Q71473129)
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description scientific article published on September 1, 1997

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