Famillial pericentric inversion of chromosome 9, INV (9)(p22q32) with recurrent duplication-deletion.
- Published in:
- Clinical Genetics, 1983, v. 24, n. 3, p. 220, doi. 10.1111/j.1399-0004.1983.tb02243.x
- Publication type:
- Article
Works matching IS 00099163 AND DT 1983 AND VI 24 AND IP 3
Results: 16
1
2
A new from of residual hexosaminidase activity in infantile Tay Sachs disease fibroblasts.
- Published in:
- Clinical Genetics, 1983, v. 24, n. 3, p. 206, doi. 10.1111/j.1399-0004.1983.tb02241.x
- By:
- Publication type:
- Article
3
Cytogentic studies of a patient with mosaicism of isochromosome 13q and a dicentric (Y; 13) translocation showing differential centromeric activity.
- Published in:
- Clinical Genetics, 1983, v. 24, n. 3, p. 194, doi. 10.1111/j.1399-0004.1983.tb02239.x
- By:
- Publication type:
- Article
4
A New Solution to Procreation.
- Published in:
- Clinical Genetics, 1983, v. 24, n. 3, p. 223, doi. 10.1111/j.1399-0004.1983.tb02244.x
- By:
- Publication type:
- Article
5
An HLA-All Assoiciation with the hemochromatosis allele?
- Published in:
- Clinical Genetics, 1983, v. 24, n. 3, p. 171, doi. 10.1111/j.1399-0004.1983.tb02234.x
- By:
- Publication type:
- Article
6
A further case of monosomy 10qter.
- Published in:
- Clinical Genetics, 1983, v. 24, n. 3, p. 216, doi. 10.1111/j.1399-0004.1983.tb02242.x
- By:
- Publication type:
- Article
7
Folic acid metabolism in patient with fragile X.
- Published in:
- Clinical Genetics, 1983, v. 24, n. 3, p. 153, doi. 10.1111/j.1399-0004.1983.tb02231.x
- By:
- Publication type:
- Article
8
Frontonasal dysplasia, coronal cranisoynostosis, pre- and postaxial polydactyly and split nails: a new autosomal dominant mutant with reduced penetrance and varibale expression?
- Published in:
- Clinical Genetics, 1983, v. 24, n. 3, p. 200, doi. 10.1111/j.1399-0004.1983.tb02240.x
- By:
- Publication type:
- Article
9
The Sixth Annual New York March of Dimes Symposium on Genetics for the Practicing Physician.
- Published in:
- Clinical Genetics, 1983, v. 24, n. 3, p. 152, doi. 10.1111/j.1399-0004.1983.tb02230.x
- Publication type:
- Article
10
The half chromatid mutation model and bidrectional mutation in incontinentia pigmenti.
- Published in:
- Clinical Genetics, 1983, v. 24, n. 3, p. 177, doi. 10.1111/j.1399-0004.1983.tb02235.x
- By:
- Publication type:
- Article
11
Replication and inactivation of and isodicentric X: presence of an inactive centromere influences the replication patterns.
- Published in:
- Clinical Genetics, 1983, v. 24, n. 3, p. 180, doi. 10.1111/j.1399-0004.1983.tb02236.x
- By:
- Publication type:
- Article
12
Letter to the Editors.
- Published in:
- Clinical Genetics, 1983, v. 24, n. 3, p. 151, doi. 10.1111/j.1399-0004.1983.tb02229.x
- By:
- Publication type:
- Article
13
Dominant ano-rectal malfromatin, nephritis and nerve-deafness: a possible new entity?
- Published in:
- Clinical Genetics, 1983, v. 24, n. 3, p. 191, doi. 10.1111/j.1399-0004.1983.tb02238.x
- By:
- Publication type:
- Article
14
Is there a predisposition for meiotic non-disjunciton that may be detected by mitoitc hyperploidy?
- Published in:
- Clinical Genetics, 1983, v. 24, n. 3, p. 184, doi. 10.1111/j.1399-0004.1983.tb02237.x
- By:
- Publication type:
- Article
15
Germinal mosaicism in achondroplasia: a family with 3 affected siblings of normal parents.
- Published in:
- Clinical Genetics, 1983, v. 24, n. 3, p. 156, doi. 10.1111/j.1399-0004.1983.tb02232.x
- By:
- Publication type:
- Article
16
Gentics and linkage relationships of the C3 polymorphism: discovery of C3-Se linkage and assignment of LES-C3-DM-Se-PEPD-Lu synteny to chromosome 19.
- Published in:
- Clinical Genetics, 1983, v. 24, n. 3, p. 159, doi. 10.1111/j.1399-0004.1983.tb02233.x
- By:
- Publication type:
- Article