Amniotic fluid folate, vitamin B.
- Published in:
- Clinical Genetics, 1988, v. 33, n. 6, p. 441, doi. 10.1111/j.1399-0004.1988.tb03478.x
- By:
- Publication type:
- Article
Works matching IS 00099163 AND DT 1988 AND VI 33 AND IP 6
Results: 12
1
2
Carrier detection in Sanfilippo A syndrome.
- Published in:
- Clinical Genetics, 1988, v. 33, n. 6, p. 401, doi. 10.1111/j.1399-0004.1988.tb03471.x
- By:
- Publication type:
- Article
3
Unusual segregation in a family with a 11/21 translocation.
- Published in:
- Clinical Genetics, 1988, v. 33, n. 6, p. 449, doi. 10.1111/j.1399-0004.1988.tb03479.x
- By:
- Publication type:
- Article
4
Familial partial trisomy 5p resulting from segregation of an insertional translocation.
- Published in:
- Clinical Genetics, 1988, v. 33, n. 6, p. 404, doi. 10.1111/j.1399-0004.1988.tb03472.x
- By:
- Publication type:
- Article
5
The fragile X-chromosome: an evaluation of the results in a routine cytogenetic laboratory in the period 1981-1986.
- Published in:
- Clinical Genetics, 1988, v. 33, n. 6, p. 410, doi. 10.1111/j.1399-0004.1988.tb03473.x
- By:
- Publication type:
- Article
6
Selective immunodeficiency with defect in interferon-gamma induction in two sibs with recurrent infections.
- Published in:
- Clinical Genetics, 1988, v. 33, n. 6, p. 454, doi. 10.1111/j.1399-0004.1988.tb03480.x
- By:
- Publication type:
- Article
7
Myelodysplastic syndrome in a kindred with ins(16) (p11.2).
- Published in:
- Clinical Genetics, 1988, v. 33, n. 6, p. 418, doi. 10.1111/j.1399-0004.1988.tb03474.x
- By:
- Publication type:
- Article
8
The 49,XXXXY syndrome. Clinical and psychological follow-up data.
- Published in:
- Clinical Genetics, 1988, v. 33, n. 6, p. 429, doi. 10.1111/j.1399-0004.1988.tb03476.x
- By:
- Publication type:
- Article
9
Abstracts.
- Published in:
- Clinical Genetics, 1988, v. 33, n. 6, p. 460, doi. 10.1111/j.1399-0004.1988.tb03482.x
- Publication type:
- Article
10
Heterogeneity of dominant high-frequency sensorineural deafness.
- Published in:
- Clinical Genetics, 1988, v. 33, n. 6, p. 424, doi. 10.1111/j.1399-0004.1988.tb03475.x
- By:
- Publication type:
- Article
11
A linkage study of the locus for X-linked Charcot-Marie-Tooth disease.
- Published in:
- Clinical Genetics, 1988, v. 33, n. 6, p. 435, doi. 10.1111/j.1399-0004.1988.tb03477.x
- By:
- Publication type:
- Article
12
The Prader-Willi syndrome and the Sotos syndrome: syndromes or sequences?
- Published in:
- Clinical Genetics, 1988, v. 33, n. 6, p. 457, doi. 10.1111/j.1399-0004.1988.tb03481.x
- By:
- Publication type:
- Article