Convoluted cells as a marker for maternal cell contamination in CVS cultures.
- Published in:
- Clinical Genetics, 1987, v. 31, n. 6, p. 410, doi. 10.1111/j.1399-0004.1987.tb02834.x
- By:
- Publication type:
- Article
Works matching IS 00099163 AND DT 1987 AND VI 31 AND IP 6
Results: 16
1
2
Supernumary marker chromosomes in a mentally retarded population identified as in vdup(15).
- Published in:
- Clinical Genetics, 1987, v. 31, n. 6, p. 425, doi. 10.1111/j.1399-0004.1987.tb02837.x
- By:
- Publication type:
- Article
3
Letter to the Editors.
- Published in:
- Clinical Genetics, 1987, v. 31, n. 6, p. 429, doi. 10.1111/j.1399-0004.1987.tb02838.x
- By:
- Publication type:
- Article
4
Familial transmission of Wolf syndrome resulting from specific deletion 4p16 from t(4;8)(p16;p21) mat.
- Published in:
- Clinical Genetics, 1987, v. 31, n. 6, p. 366, doi. 10.1111/j.1399-0004.1987.tb02825.x
- By:
- Publication type:
- Article
5
Three cases of partial trisomy 9q in one generation due to maternal reciprocal t(6;8;9) translocation.
- Published in:
- Clinical Genetics, 1987, v. 31, n. 6, p. 359, doi. 10.1111/j.1399-0004.1987.tb02824.x
- By:
- Publication type:
- Article
6
Pallister-Killian syndrome: cytogenetic and molecular studies.
- Published in:
- Clinical Genetics, 1987, v. 31, n. 6, p. 399, doi. 10.1111/j.1399-0004.1987.tb02832.x
- By:
- Publication type:
- Article
7
The Brachmann-de Lange syndrome in two siblings of normal parents.
- Published in:
- Clinical Genetics, 1987, v. 31, n. 6, p. 413, doi. 10.1111/j.1399-0004.1987.tb02835.x
- By:
- Publication type:
- Article
8
Deletion of the short arm of chromosome 20.
- Published in:
- Clinical Genetics, 1987, v. 31, n. 6, p. 406, doi. 10.1111/j.1399-0004.1987.tb02833.x
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- Publication type:
- Article
9
Announcement.
- Published in:
- Clinical Genetics, 1987, v. 31, n. 6, p. 430, doi. 10.1111/j.1399-0004.1987.tb02839.x
- Publication type:
- Article
10
Autosomal dominant epidermolysis bullosa dystrophics: are the Cockayne- Touraine, the Pasini and the Bart-types different expressions of the same mutant gene?
- Published in:
- Clinical Genetics, 1987, v. 31, n. 6, p. 416, doi. 10.1111/j.1399-0004.1987.tb02836.x
- By:
- Publication type:
- Article
11
Centric fission, centromere-telomere fusion and isochromosome formation: a possible origin of a de novo 12p trisomy.
- Published in:
- Clinical Genetics, 1987, v. 31, n. 6, p. 393, doi. 10.1111/j.1399-0004.1987.tb02831.x
- By:
- Publication type:
- Article
12
Autosomal dominant inheritance of cervical ribs.
- Published in:
- Clinical Genetics, 1987, v. 31, n. 6, p. 386, doi. 10.1111/j.1399-0004.1987.tb02829.x
- By:
- Publication type:
- Article
13
Single maxillary central incisor and coloboma in hypomelanosis of Ko.
- Published in:
- Clinical Genetics, 1987, v. 31, n. 6, p. 370, doi. 10.1111/j.1399-0004.1987.tb02826.x
- By:
- Publication type:
- Article
14
A patient with onychotrichodysplasia, neutropenia and normal intelligence.
- Published in:
- Clinical Genetics, 1987, v. 31, n. 6, p. 374, doi. 10.1111/j.1399-0004.1987.tb02827.x
- By:
- Publication type:
- Article
15
A Japanese patient with the Dubowitz syndrome.
- Published in:
- Clinical Genetics, 1987, v. 31, n. 6, p. 389, doi. 10.1111/j.1399-0004.1987.tb02830.x
- By:
- Publication type:
- Article
16
Trisomy 2q and monosomy 11q in the same individual: the importance of considering the deleted segment.
- Published in:
- Clinical Genetics, 1987, v. 31, n. 6, p. 381, doi. 10.1111/j.1399-0004.1987.tb02828.x
- By:
- Publication type:
- Article