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De Novo variants in the KMT2A (MLL) gene causing atypical Wiedemann-Steiner syndrome in two unrelated individuals identified by clinical exome sequencing.
BMC Med Genet. 2014 May 1;15:49. doi: 10.1186/1471-2350-15-49.
BMC Med Genet. 2014.
PMID: 24886118
Free PMC article.
Juvenile rheumatoid arthritis and del(22q11) syndrome: a non-random association.
Verloes A, Curry C, Jamar M, Herens C, O'Lague P, Marks J, Sarda P, Blanchet P.
Verloes A, et al.
J Med Genet. 1998 Nov;35(11):943-7. doi: 10.1136/jmg.35.11.943.
J Med Genet. 1998.
PMID: 9832043
Free PMC article.
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Mild autosomal dominant hypophosphatasia: in utero presentation in two families.
Moore CA, Curry CJ, Henthorn PS, Smith JA, Smith JC, O'Lague P, Coburn SP, Weaver DD, Whyte MP.
Moore CA, et al.
Am J Med Genet. 1999 Oct 29;86(5):410-5. doi: 10.1002/(sici)1096-8628(19991029)86:5<410::aid-ajmg3>3.0.co;2-0.
Am J Med Genet. 1999.
PMID: 10508980
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ATFresno: a phenotype linking ataxia-telangiectasia with the Nijmegen breakage syndrome.
Curry CJ, O'Lague P, Tsai J, Hutchison HT, Jaspers NG, Wara D, Gatti RA.
Curry CJ, et al.
Am J Hum Genet. 1989 Aug;45(2):270-5.
Am J Hum Genet. 1989.
PMID: 2491181
Free PMC article.
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Elucidation of the cytogenetic abnormality in a 4p- "phenocopy".
Curry CJ, Ying KL, O'Lague P, Tsai J.
Curry CJ, et al.
Birth Defects Orig Artic Ser. 1982;18(3B):275-86.
Birth Defects Orig Artic Ser. 1982.
PMID: 7139110
No abstract available.
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Inherited chondrodysplasia punctata due to a deletion of the terminal short arm of an X chromosome.
Curry CJ, Magenis RE, Brown M, Lanman JT Jr, Tsai J, O'Lague P, Goodfellow P, Mohandas T, Bergner EA, Shapiro LJ.
Curry CJ, et al.
N Engl J Med. 1984 Oct 18;311(16):1010-5. doi: 10.1056/NEJM198410183111603.
N Engl J Med. 1984.
PMID: 6482910
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