Association of DNA-haplotypes in the human LDL-receptor gene with normal serum cholesterol levels.
- Published in:
- Clinical Genetics, 1990, v. 38, n. 6, p. 401, doi. 10.1111/j.1399-0004.1990.tb03604.x
- By:
- Publication type:
- Article
Works matching IS 00099163 AND DT 1990 AND VI 38 AND IP 6
Results: 14
1
2
Craniofrontonasal dysostosis: variable expression in a three-generation family.
- Published in:
- Clinical Genetics, 1990, v. 38, n. 6, p. 441, doi. 10.1111/j.1399-0004.1990.tb03610.x
- By:
- Publication type:
- Article
3
Clinical expression of Menkes syndrome in females.
- Published in:
- Clinical Genetics, 1990, v. 38, n. 6, p. 452, doi. 10.1111/j.1399-0004.1990.tb03612.x
- By:
- Publication type:
- Article
4
Common intragenic and extragenic polymorphisms of blood coagulation factors VIII and IX are different in Chinese and Caucasian populations.
- Published in:
- Clinical Genetics, 1990, v. 38, n. 6, p. 434, doi. 10.1111/j.1399-0004.1990.tb03609.x
- By:
- Publication type:
- Article
5
An isolated case of Duchenne muscular dystrophy (DMD) in a female with a deletion of DMD cDNA.
- Published in:
- Clinical Genetics, 1990, v. 38, n. 6, p. 474, doi. 10.1111/j.1399-0004.1990.tb03616.x
- By:
- Publication type:
- Article
6
Homozygous C4A deficiency in systemic lupus erythematosus: analysis of patients from a defined population.
- Published in:
- Clinical Genetics, 1990, v. 38, n. 6, p. 427, doi. 10.1111/j.1399-0004.1990.tb03608.x
- By:
- Publication type:
- Article
7
Exclusion mapping of the Cohen syndrome gene from the Prader-Willi syndrome locus.
- Published in:
- Clinical Genetics, 1990, v. 38, n. 6, p. 422, doi. 10.1111/j.1399-0004.1990.tb03607.x
- By:
- Publication type:
- Article
8
Excess of HLA parental sharing in families with Turner patients.
- Published in:
- Clinical Genetics, 1990, v. 38, n. 6, p. 415, doi. 10.1111/j.1399-0004.1990.tb03606.x
- By:
- Publication type:
- Article
9
Re-evaluation of GM2346 from a del(16)(q22) to t(4;16)(q35;q22.1).
- Published in:
- Clinical Genetics, 1990, v. 38, n. 6, p. 466, doi. 10.1111/j.1399-0004.1990.tb03614.x
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- Publication type:
- Article
10
A possible relationship between Beckwith-Wiedemann syndrome, urinary tract anomaly and prune belly syndrome.
- Published in:
- Clinical Genetics, 1990, v. 38, n. 6, p. 410, doi. 10.1111/j.1399-0004.1990.tb03605.x
- By:
- Publication type:
- Article
11
Emery-Dreifuss syndrome in three generations of females, including identical twins.
- Published in:
- Clinical Genetics, 1990, v. 38, n. 6, p. 447, doi. 10.1111/j.1399-0004.1990.tb03611.x
- By:
- Publication type:
- Article
12
Diagnosis of familial amyloidotic polyneuropathy in France.
- Published in:
- Clinical Genetics, 1990, v. 38, n. 6, p. 469, doi. 10.1111/j.1399-0004.1990.tb03615.x
- By:
- Publication type:
- Article
13
Attitudes of parents of cystic fibrosis children towards neonatal screening and antenatal diagnosis.
- Published in:
- Clinical Genetics, 1990, v. 38, n. 6, p. 460, doi. 10.1111/j.1399-0004.1990.tb03613.x
- By:
- Publication type:
- Article
14
Announcements.
- Published in:
- Clinical Genetics, 1990, v. 38, n. 6, p. 479, doi. 10.1111/j.1399-0004.1990.tb03617.x
- Publication type:
- Article