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PubMed (OMIM) for id: 68625
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Narrowing the candidate region for congenital diaphragmatic hernia in chromosome 15q26: contradictory results.
Am J Hum Genet. 2005 Nov;77(5):892-4; author reply 894-5. doi: 10.1086/497082.
Am J Hum Genet. 2005.
PMID: 16252246
Free PMC article.
No abstract available.
Fryns syndrome phenotype caused by chromosome microdeletions at 15q26.2 and 8p23.1.
Slavotinek A, Lee SS, Davis R, Shrit A, Leppig KA, Rhim J, Jasnosz K, Albertson D, Pinkel D.
Slavotinek A, et al.
J Med Genet. 2005 Sep;42(9):730-6. doi: 10.1136/jmg.2004.028787.
J Med Genet. 2005.
PMID: 16141010
Free PMC article.
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Congenital diaphragmatic hernia and chromosome 15q26: determination of a candidate region by use of fluorescent in situ hybridization and array-based comparative genomic hybridization.
Klaassens M, van Dooren M, Eussen HJ, Douben H, den Dekker AT, Lee C, Donahoe PK, Galjaard RJ, Goemaere N, de Krijger RR, Wouters C, Wauters J, Oostra BA, Tibboel D, de Klein A.
Klaassens M, et al.
Am J Hum Genet. 2005 May;76(5):877-82. doi: 10.1086/429842. Epub 2005 Mar 4.
Am J Hum Genet. 2005.
PMID: 15750894
Free PMC article.
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