Normal testicular histology in a mid-trimester 49,XXXXY fetus.
- Published in:
- Clinical Genetics, 1995, v. 47, n. 6, p. 331, doi. 10.1111/j.1399-0004.1995.tb03977.x
- By:
- Publication type:
- Article
Works matching IS 00099163 AND DT 1995 AND VI 47 AND IP 6
Results: 15
1
2
Problems arising in correlating clinical and molecular data in myotonic dystrophy.
- Published in:
- Clinical Genetics, 1995, v. 47, n. 6, p. 302, doi. 10.1111/j.1399-0004.1995.tb03969.x
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- Publication type:
- Article
3
A Taql polymorphism in a gene belonging to the human apoprotein(a)-plasminogen gene family on the telomeric region of chromosome 6 (6q26-27).
- Published in:
- Clinical Genetics, 1995, v. 47, n. 6, p. 330, doi. 10.1111/j.1399-0004.1995.tb03976.x
- By:
- Publication type:
- Article
4
Aplasia cutis congenita and associated disorders: an update.
- Published in:
- Clinical Genetics, 1995, v. 47, n. 6, p. 295, doi. 10.1111/j.1399-0004.1995.tb03968.x
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- Publication type:
- Article
5
Genetic analysis of 20 families with autosomal dominant adult polycystic kidney disease from South West Thames Region.
- Published in:
- Clinical Genetics, 1995, v. 47, n. 6, p. 290, doi. 10.1111/j.1399-0004.1995.tb03967.x
- By:
- Publication type:
- Article
6
A further report of Brachmann-de Lange syndrome in two sibs with normal parents.
- Published in:
- Clinical Genetics, 1995, v. 47, n. 6, p. 324, doi. 10.1111/j.1399-0004.1995.tb03974.x
- By:
- Publication type:
- Article
7
Video display terminals: risk of trisomy 18?
- Published in:
- Clinical Genetics, 1995, v. 47, n. 6, p. 335, doi. 10.1111/j.1399-0004.1995.tb03979.x
- By:
- Publication type:
- Article
8
Cystic fibrosis mutations and immotile cilia syndrome.
- Published in:
- Clinical Genetics, 1995, v. 47, n. 6, p. 328, doi. 10.1111/j.1399-0004.1995.tb03975.x
- By:
- Publication type:
- Article
9
Identification of a breast tumor with microsatellite instability in a potential carrier of the hereditary non-polyposis colon cancer trait.
- Published in:
- Clinical Genetics, 1995, v. 47, n. 6, p. 305, doi. 10.1111/j.1399-0004.1995.tb03970.x
- By:
- Publication type:
- Article
10
Detection of α-thalassemia-1 (Southeast Asian type) and its application for prenatal diagnosis.
- Published in:
- Clinical Genetics, 1995, v. 47, n. 6, p. 318, doi. 10.1111/j.1399-0004.1995.tb03972.x
- By:
- Publication type:
- Article
11
Retinoblastoma in association with the chromosome breakage syndromes Fanconi's anaemia and Bloom's syndrome: clinical and cytogenetic findings.
- Published in:
- Clinical Genetics, 1995, v. 47, n. 6, p. 311, doi. 10.1111/j.1399-0004.1995.tb03971.x
- By:
- Publication type:
- Article
12
Screening of neurofibromatosis type 1 gene: identification of a large deletion and of an intronic variant.
- Published in:
- Clinical Genetics, 1995, v. 47, n. 6, p. 281, doi. 10.1111/j.1399-0004.1995.tb03965.x
- By:
- Publication type:
- Article
13
A recombination event in the closely linked plasminogen and apolipoprotein(a) gene loci.
- Published in:
- Clinical Genetics, 1995, v. 47, n. 6, p. 285, doi. 10.1111/j.1399-0004.1995.tb03966.x
- By:
- Publication type:
- Article
14
Constitutional heteromorphism of 9q13→q21 in a patient with chronic myelogenous leukemia.
- Published in:
- Clinical Genetics, 1995, v. 47, n. 6, p. 321, doi. 10.1111/j.1399-0004.1995.tb03973.x
- By:
- Publication type:
- Article
15
Clinical follow up of a girl with 'mental retardation with pterygia, shortness and distinct facial appearance' (Haspeslagh syndrome).
- Published in:
- Clinical Genetics, 1995, v. 47, n. 6, p. 332, doi. 10.1111/j.1399-0004.1995.tb03978.x
- By:
- Publication type:
- Article