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Consideration of VACTERL association in patients with trisomy 21.

作者信息

Solomon Benjamin D, Bous Sophia M, Bianconi Simona, Pineda-Alvarez Daniel E

机构信息

Medical Genetics Branch, National Human Genome Research Institute, National Institutes of Health Program in Developmental Endocrinology and Genetics, Eunice Kennedy Shriver National Institute of Child Health and Human Development, National Institutes of Health, Bethesda, Maryland, USA.

出版信息

Clin Dysmorphol. 2010 Oct;19(4):209-211. doi: 10.1097/MCD.0b013e32833b2b9c.

Abstract
摘要

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本文引用的文献

1
Evidence for inheritance in patients with VACTERL association.
Hum Genet. 2010 Jun;127(6):731-3. doi: 10.1007/s00439-010-0814-7. Epub 2010 Apr 6.
2
Congenital defects among liveborn infants with Down syndrome.
Birth Defects Res A Clin Mol Teratol. 2007 Sep;79(9):657-63. doi: 10.1002/bdra.20393.
3
Down syndrome and scoliosis: a review of a 50-year experience at one institution.
Spine (Phila Pa 1976). 2005 Sep 15;30(18):2051-5. doi: 10.1097/01.brs.0000179100.54453.72.
4
VATERL: an epidemiologic analysis of risk factors.
Am J Med Genet. 1997 Dec 12;73(2):162-9. doi: 10.1002/(sici)1096-8628(1997)73:2<162::aid-ajmg10>3.0.co;2-s.
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The spectrum of congenital anomalies of the VATER association: an international study.
Am J Med Genet. 1997 Jul 11;71(1):8-15. doi: 10.1002/(sici)1096-8628(19970711)71:1<8::aid-ajmg2>3.0.co;2-v.

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