Roberts-SC phocomelia syndrome: a case with additional anomalies.
- Published in:
- Clinical Genetics, 1994, v. 45, n. 2, p. 107, doi. 10.1111/j.1399-0004.1994.tb04004.x
- By:
- Publication type:
- Article
Works matching IS 00099163 AND DT 1994 AND VI 45 AND IP 2
Results: 13
1
2
Minimal genetic influences on plasma fibrinogen level in adult males in the NHLBI twin study.
- Published in:
- Clinical Genetics, 1994, v. 45, n. 2, p. 71, doi. 10.1111/j.1399-0004.1994.tb03997.x
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- Publication type:
- Article
3
A woman with an apparent non-mosaic 45,X delivered a 46,X,der(X) liveborn female.
- Published in:
- Clinical Genetics, 1994, v. 45, n. 2, p. 93, doi. 10.1111/j.1399-0004.1994.tb04001.x
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- Publication type:
- Article
4
Autosomal dominant inheritance of thyroglossal duct cyst.
- Published in:
- Clinical Genetics, 1994, v. 45, n. 2, p. 111, doi. 10.1111/j.1399-0004.1994.tb04006.x
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- Publication type:
- Article
5
Duchenne muscular dystrophy and spinal muscular atrophy type I segregating in the same family.
- Published in:
- Clinical Genetics, 1994, v. 45, n. 2, p. 97, doi. 10.1111/j.1399-0004.1994.tb04002.x
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- Publication type:
- Article
6
A new human mtDNA polymorphism: tRNAGln/4336 (T→C).
- Published in:
- Clinical Genetics, 1994, v. 45, n. 2, p. 109, doi. 10.1111/j.1399-0004.1994.tb04005.x
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- Publication type:
- Article
7
A fluorescent in situ hybridization analysis of the chromosome constitution of ejaculated sperm in a 47, XYY male.
- Published in:
- Clinical Genetics, 1994, v. 45, n. 2, p. 67, doi. 10.1111/j.1399-0004.1994.tb03996.x
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- Publication type:
- Article
8
Apolipoprotein B gene polymorphisms in ischemic heart disease and hypercholesterolemia: effects of age and sex.
- Published in:
- Clinical Genetics, 1994, v. 45, n. 2, p. 78, doi. 10.1111/j.1399-0004.1994.tb03998.x
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- Publication type:
- Article
9
Chromosome instability in lymphocytes from patients with celiac disease.
- Published in:
- Clinical Genetics, 1994, v. 45, n. 2, p. 57, doi. 10.1111/j.1399-0004.1994.tb03994.x
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- Publication type:
- Article
10
Non-expression of von Hippel-Lindau phenotype in an obligate gene carrier.
- Published in:
- Clinical Genetics, 1994, v. 45, n. 2, p. 104, doi. 10.1111/j.1399-0004.1994.tb04003.x
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- Publication type:
- Article
11
Metaphase quality can be monitored by automatic counting of bands.
- Published in:
- Clinical Genetics, 1994, v. 45, n. 2, p. 62, doi. 10.1111/j.1399-0004.1994.tb03995.x
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- Publication type:
- Article
12
An 87 bp deletion in exon 5 of the LDL receptor gene in a mother and her son with familial hypercholesterolemia.
- Published in:
- Clinical Genetics, 1994, v. 45, n. 2, p. 84, doi. 10.1111/j.1399-0004.1994.tb03999.x
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- Publication type:
- Article
13
The gene for familial dystonia with myoclonic jerks responsive to alcohol is not located on the distal end of 9q.
- Published in:
- Clinical Genetics, 1994, v. 45, n. 2, p. 88, doi. 10.1111/j.1399-0004.1994.tb04000.x
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- Publication type:
- Article