Escape of the yolk sac: a hypothesis to explain the embryogenesis of gastroschisis.
- Published in:
- Clinical Genetics, 2009, v. 75, n. 4, p. 326, doi. 10.1111/j.1399-0004.2008.01142.x
- By:
- Publication type:
- Article
Works matching IS 00099163 AND DT 2009 AND VI 75 AND IP 4
Results: 15
1
2
Novel FAM83H mutations in Turkish families with autosomal dominant hypocalcified amelogenesis imperfecta.
- Published in:
- 2009
- By:
- Publication type:
- Letter
3
Identification and characterization of novel uroporphyrinogen decarboxylase gene mutations in a large series of porphyria cutanea tarda patients and relatives.
- Published in:
- Clinical Genetics, 2009, v. 75, n. 4, p. 346, doi. 10.1111/j.1399-0004.2009.01153.x
- By:
- Publication type:
- Article
4
Dominant versus recessive traits conveyed by allelic mutations – to what extent is nonsense-mediated decay involved?
- Published in:
- Clinical Genetics, 2009, v. 75, n. 4, p. 394, doi. 10.1111/j.1399-0004.2008.01114.x
- By:
- Publication type:
- Article
5
Carrier frequency of the R778L, A874V, and N1270S mutations in the ATP7B gene in a Korean population.
- Published in:
- 2009
- By:
- Publication type:
- Letter
6
A functional network module for Smith–Magenis syndrome.
- Published in:
- Clinical Genetics, 2009, v. 75, n. 4, p. 364, doi. 10.1111/j.1399-0004.2008.01135.x
- By:
- Publication type:
- Article
7
Clinical features of microdeletion 9q22.3 (pat).
- Published in:
- Clinical Genetics, 2009, v. 75, n. 4, p. 384, doi. 10.1111/j.1399-0004.2008.01141.x
- By:
- Publication type:
- Article
8
Penetrance and clinical consequences of a gross SDHB deletion in a large family.
- Published in:
- Clinical Genetics, 2009, v. 75, n. 4, p. 354, doi. 10.1111/j.1399-0004.2009.01157.x
- By:
- Publication type:
- Article
9
Germ line MLH1 and MSH2 mutations in Taiwanese Lynch syndrome families: characterization of a founder genomic mutation in the MLH1 gene.
- Published in:
- Clinical Genetics, 2009, v. 75, n. 4, p. 334, doi. 10.1111/j.1399-0004.2009.01162.x
- By:
- Publication type:
- Article
10
Gastroschisis: etiology and developmental pathogenesis.
- Published in:
- Clinical Genetics, 2009, v. 75, n. 4, p. 322, doi. 10.1111/j.1399-0004.2009.01164.x
- By:
- Publication type:
- Article
11
Omani-type spondyloepiphyseal dysplasia with cardiac involvement caused by a missense mutation in CHST3.
- Published in:
- Clinical Genetics, 2009, v. 75, n. 4, p. 375, doi. 10.1111/j.1399-0004.2009.01167.x
- By:
- Publication type:
- Article
12
PCSK1 variants: genetic risk factors for obesity.
- Published in:
- Clinical Genetics, 2009, v. 75, n. 4, p. 318, doi. 10.1111/j.1399-0004.2009.01171_1.x
- By:
- Publication type:
- Article
13
CASK: a scaffold protein involved in X-linked brain malformation phenotypes.
- Published in:
- Clinical Genetics, 2009, v. 75, n. 4, p. 319, doi. 10.1111/j.1399-0004.2009.01171_2.x
- By:
- Publication type:
- Article
14
ZFP57 mutations cause an autosomal recessive imprinting disorder.
- Published in:
- Clinical Genetics, 2009, v. 75, n. 4, p. 320, doi. 10.1111/j.1399-0004.2009.01171_3.x
- By:
- Publication type:
- Article
15
Plumbing in the embryo: developmental defects of the urinary tracts.
- Published in:
- Clinical Genetics, 2009, v. 75, n. 4, p. 307, doi. 10.1111/j.1399-0004.2009.01175.x
- By:
- Publication type:
- Article