A linkage study of malignant hyperthermia (MH).
- Published in:
- Clinical Genetics, 1990, v. 37, n. 3, p. 221, doi. 10.1111/j.1399-0004.1990.tb03506.x
- By:
- Publication type:
- Article
Works matching IS 00099163 AND DT 1990 AND VI 37 AND IP 3
Results: 16
1
2
A child with cystic fibrosis: II. Subsequent family planning decisions, reproduction and use of prenatal diagnosis.
- Published in:
- Clinical Genetics, 1990, v. 37, n. 3, p. 207, doi. 10.1111/j.1399-0004.1990.tb03504.x
- By:
- Publication type:
- Article
3
The common fragile site in band q27 of the human X chromosome is not coincident with the fragile X.
- Published in:
- Clinical Genetics, 1990, v. 37, n. 3, p. 167, doi. 10.1111/j.1399-0004.1990.tb03498.x
- By:
- Publication type:
- Article
4
Three-generation transmission of Hirschsprung's disease.
- Published in:
- Clinical Genetics, 1990, v. 37, n. 3, p. 235, doi. 10.1111/j.1399-0004.1990.tb03509.x
- By:
- Publication type:
- Article
5
Proximal 15q variant as possible pitfall in the cytogenetic diagnosis of Prader-Willi syndrome.
- Published in:
- Clinical Genetics, 1990, v. 37, n. 3, p. 161, doi. 10.1111/j.1399-0004.1990.tb03497.x
- By:
- Publication type:
- Article
6
Apolipoprotein A-l/C-lll gene cluster polymorphism in Saudi Arabians, Filipinos and Caucasians.
- Published in:
- Clinical Genetics, 1990, v. 37, n. 3, p. 194, doi. 10.1111/j.1399-0004.1990.tb03502.x
- By:
- Publication type:
- Article
7
Announcements.
- Published in:
- Clinical Genetics, 1990, v. 37, n. 3, p. 239, doi. 10.1111/j.1399-0004.1990.tb03512.x
- Publication type:
- Article
8
A child with cystic fibrosis: I. Parental knowledge about the genetic transmission of CF and about DNA-diagnostic procedures.
- Published in:
- Clinical Genetics, 1990, v. 37, n. 3, p. 198, doi. 10.1111/j.1399-0004.1990.tb03503.x
- By:
- Publication type:
- Article
9
High resolution banding of an unusual reciprocal translocation in recurrent abortions.
- Published in:
- Clinical Genetics, 1990, v. 37, n. 3, p. 230, doi. 10.1111/j.1399-0004.1990.tb03508.x
- By:
- Publication type:
- Article
10
A case of 46,XX,r(X) (p1q1) diagnosed by in situ hybridization.
- Published in:
- Clinical Genetics, 1990, v. 37, n. 3, p. 216, doi. 10.1111/j.1399-0004.1990.tb03505.x
- By:
- Publication type:
- Article
11
Terminal 7q deletion as a cause of holoprosencephaly.
- Published in:
- Clinical Genetics, 1990, v. 37, n. 3, p. 238, doi. 10.1111/j.1399-0004.1990.tb03511.x
- By:
- Publication type:
- Article
12
Genetic counselling in Duchenne and Becker muscular dystrophy is problematic when carrier studies give controversial results.
- Published in:
- Clinical Genetics, 1990, v. 37, n. 3, p. 179, doi. 10.1111/j.1399-0004.1990.tb03500.x
- By:
- Publication type:
- Article
13
Sotos syndrome and de novo balanced autosomal translocation (t(3;6)(p21;p21)).
- Published in:
- Clinical Genetics, 1990, v. 37, n. 3, p. 226, doi. 10.1111/j.1399-0004.1990.tb03507.x
- By:
- Publication type:
- Article
14
Comparison of anatomical location of squamous cell carcinoma within the oral cavity and oropharynx with the incidence of in vitro hyperdiploidy.
- Published in:
- Clinical Genetics, 1990, v. 37, n. 3, p. 188, doi. 10.1111/j.1399-0004.1990.tb03501.x
- By:
- Publication type:
- Article
15
Monosomy X found at first trimester CVS: a diagnostic and counselling dilemma.
- Published in:
- Clinical Genetics, 1990, v. 37, n. 3, p. 236, doi. 10.1111/j.1399-0004.1990.tb03510.x
- By:
- Publication type:
- Article
16
CSF and urine biogenic amine metabolites in Rett syndrome.
- Published in:
- Clinical Genetics, 1990, v. 37, n. 3, p. 173, doi. 10.1111/j.1399-0004.1990.tb03499.x
- By:
- Publication type:
- Article