Complete and partial trisomy 8.
- Published in:
- Clinical Genetics, 1980, v. 18, n. 4, p. 314, doi. 10.1111/j.1399-0004.1980.tb00891.x
- By:
- Publication type:
- Article
Works matching IS 00099163 AND DT 1980 AND VI 18 AND IP 4
Results: 15
1
2
Peculiar face, pectus carinatum and joint laxity in brother and sister.
- Published in:
- Clinical Genetics, 1980, v. 18, n. 4, p. 280, doi. 10.1111/j.1399-0004.1980.tb00886.x
- By:
- Publication type:
- Article
3
Idiopathic intestinal pseudo-obstruction: A familial visceral neuropathy.
- Published in:
- Clinical Genetics, 1980, v. 18, n. 4, p. 291, doi. 10.1111/j.1399-0004.1980.tb00888.x
- By:
- Publication type:
- Article
4
Trisomy 18q: 46, XX,13q+,t(13;18)(q32;q11) in a newborn associated with multiple congenital anomalies due to paternal reciprocal translocation, 46, XY,-13,+der(13)/t(13;18)(q32;q11).
- Published in:
- Clinical Genetics, 1980, v. 18, n. 4, p. 233, doi. 10.1111/j.1399-0004.1980.tb00879.x
- By:
- Publication type:
- Article
5
A new syndrome of triphalangeal thumbs and brachy-ectrodactyly.
- Published in:
- Clinical Genetics, 1980, v. 18, n. 4, p. 244, doi. 10.1111/j.1399-0004.1980.tb00881.x
- By:
- Publication type:
- Article
6
X-linked Dyggve-Melchior-Clausen syndrome.
- Published in:
- Clinical Genetics, 1980, v. 18, n. 4, p. 284, doi. 10.1111/j.1399-0004.1980.tb00887.x
- By:
- Publication type:
- Article
7
Distal osteosclerosis.
- Published in:
- Clinical Genetics, 1980, v. 18, n. 4, p. 298, doi. 10.1111/j.1399-0004.1980.tb00889.x
- By:
- Publication type:
- Article
8
Interstitial deletion of the long arm of chromosome 1, del(1)(q21-q25) in a profoundly retarded 8-year-old girl with multiple anomalies.
- Published in:
- Clinical Genetics, 1980, v. 18, n. 4, p. 305, doi. 10.1111/j.1399-0004.1980.tb00890.x
- By:
- Publication type:
- Article
9
Announcement.
- Published in:
- Clinical Genetics, 1980, v. 18, n. 4, p. 316, doi. 10.1111/j.1399-0004.1980.tb00893.x
- Publication type:
- Article
10
Properties and significance of a small marker chromosome in amniotic fluid cells.
- Published in:
- Clinical Genetics, 1980, v. 18, n. 4, p. 253, doi. 10.1111/j.1399-0004.1980.tb00882.x
- By:
- Publication type:
- Article
11
Replay from R M Flneman, Utah.
- Published in:
- Clinical Genetics, 1980, v. 18, n. 4, p. 314, doi. 10.1111/j.1399-0004.1980.tb00892.x
- By:
- Publication type:
- Article
12
Amniotic fluid secretor typing: Validation for use in prenatal prediction of myotonic dystrophy.
- Published in:
- Clinical Genetics, 1980, v. 18, n. 4, p. 257, doi. 10.1111/j.1399-0004.1980.tb00883.x
- By:
- Publication type:
- Article
13
Assay of the β-glucosidase activity with natural labelled and artificial substrates in cultivated skin fibroblasts from homozygotes and heterozygotes with the Norrbottnian type of Gaucher disease.
- Published in:
- Clinical Genetics, 1980, v. 18, n. 4, p. 268, doi. 10.1111/j.1399-0004.1980.tb00884.x
- By:
- Publication type:
- Article
14
A balanced translocation t(4;9) (q35;q12) with a breakpoint within the heterochromatic region of chromosome 9 in a woman with recurrent abortion.
- Published in:
- Clinical Genetics, 1980, v. 18, n. 4, p. 239, doi. 10.1111/j.1399-0004.1980.tb00880.x
- By:
- Publication type:
- Article
15
The use of sequential silver and quinacrine staining to determine the parental origin and breakpoints of a ring-22 human chromosome.
- Published in:
- Clinical Genetics, 1980, v. 18, n. 4, p. 274, doi. 10.1111/j.1399-0004.1980.tb00885.x
- By:
- Publication type:
- Article