Found: 7
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Two siblings below the age of 20 years with diverticular disease.
- Published in:
- 2006
- By:
- Publication type:
- Letter
Recurrent and founder mutations in the Netherlands.
- Published in:
- Netherlands Heart Journal, 2010, v. 18, n. 2, p. 85, doi. 10.1007/BF03091743
- By:
- Publication type:
- Article
Homozygous and Heterozygous Expression of a Novel Insulin-Like Growth Factor-I Mutation.
- Published in:
- Journal of Clinical Endocrinology & Metabolism, 2005, v. 90, n. 5, p. 2855, doi. 10.1210/jc.2004-1254
- By:
- Publication type:
- Article
Dilatation of the Great Arteries in an Infant with Marfan Syndrome and Ventricular Septal Defect.
- Published in:
- 2011
- By:
- Publication type:
- Case Study
An unanticipated copy number variant of chromosome 15 disrupting SMAD3 reveals a three-generation family at serious risk for aortic dissection.
- Published in:
- Clinical Genetics, 2013, v. 83, n. 4, p. 337, doi. 10.1111/j.1399-0004.2012.01931.x
- By:
- Publication type:
- Article
Ehlers-Danlos arthrochalasia type (VIIA-B) - expanding the phenotype: from prenatal life through adulthood.
- Published in:
- Clinical Genetics, 2012, v. 82, n. 2, p. 121, doi. 10.1111/j.1399-0004.2011.01758.x
- By:
- Publication type:
- Article
Variable phenotypes associated with 10q23 microdeletions involving the PTEN and BMPR1A genes.
- Published in:
- Clinical Genetics, 2008, v. 74, n. 2, p. 145, doi. 10.1111/j.1399-0004.2008.01026.x
- By:
- Publication type:
- Article