Found: 7
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Screening and cell-based assessment of mutations in the Aristaless-related homeobox ( ARX) gene.
- Published in:
- Clinical Genetics, 2011, v. 80, n. 6, p. 510, doi. 10.1111/j.1399-0004.2011.01685.x
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- Publication type:
- Article
Imprinting centre deletions in two PWS families: implications for diagnostic testing and genetic counselling.
- Published in:
- Clinical Genetics, 2000, v. 58, n. 4, p. 284, doi. 10.1034/j.1399-0004.2000.580406.x
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- Publication type:
- Article
An infant with chronic articular and cutaneous manifestations: a new syndrome?
- Published in:
- 1989
- By:
- Publication type:
- journal article
An infant with chronic articular and cutaneous manifestations: a new syndrome?
- Published in:
- 1989
- By:
- Publication type:
- Case Study
Prenatal analysis of the insulin receptor gene in a family with leprechaunism.
- Published in:
- 1995
- By:
- Publication type:
- journal article
Omphalopagus conjoining and twin-twin transfusion syndrome.
- Published in:
- 2005
- By:
- Publication type:
- Case Study
Pregnancy and perinatal outcomes after assisted reproduction: a comparative study.
- Published in:
- Irish Journal of Medical Science, 2008, v. 177, n. 3, p. 233, doi. 10.1007/s11845-008-0172-9
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- Publication type:
- Article