A boy with proximal trisomy 15 and a male foetus with distal trisomy 15 due to a familial 13p;15q translocation

Clinical Genetics

Volumn 22, Issue 1, 1982, Pages 16-21

  Annerén, Göran ^a,b   Gustavson, Karl‐Henrik ^a  

^a Departments of Clinical Genetics ^*

^b UPPSALA UNIVERSITY HOSPITAL   (Sweden)

Author keywords

Chromosome 15 aneuploidy; translocation 13; 15; trisomy 15

Indexed keywords

CASE REPORT; CENTRAL NERVOUS SYSTEM; CHROMOSOME 15Q; CHROMOSOME TRANSLOCATION 13; CHROMOSOME TRANSLOCATION 15; CONGENITAL DISORDER; DIAGNOSIS; ETIOLOGY; FETUS; HEREDITY; HISTOLOGY; MENTAL RETARDATION MALFORMATION SYNDROME; PARTIAL TRISOMY 15; PHENOTYPE; PRENATAL DIAGNOSIS;

ADOLESCENT; CARRIER STATE; CASE REPORT; CHROMOSOME ABERRATIONS; CHROMOSOME DISORDERS; CHROMOSOMES, HUMAN, 13-15; HUMAN; MALE; PEDIGREE; SUPPORT, NON-U.S. GOV'T; TRANSLOCATION (GENETICS); TRISOMY;

EID: 0019903248     PISSN: 00099163     EISSN: 13990004     Source Type: Journal    
DOI: 10.1111/j.1399-0004.1982.tb01404.x     Document Type: Article

References (11)

1. A G‐like trisomy with a major 15‐proximal supernumerary component derived from a D/E balanced maternal interchange
2. Differential binding of alkylating fluochromes in human chromosomes
3. Partial trisomy of chromosome number 15 identified by trypsin‐giemsa banding
4. Inherited partial duplication of chromosome no. 15. J
5. Leucocytes cultured from small inocula of whole blood and the preparation of metaphase chromosomes by treatment with hypotonic HCI
6. Partial trisomy 15
7. Planches déscriptives des chromosomes humains. (Analyse en bandes R et nomenclature selon la conférence de Paris 1971)
8. Partial trisomy 15 and intractable seizures
9. A supernumerary “G” like chromosome originating from a maternal 13;15 translocation in a nondysmor‐phic, retarded girl
10. A case of partial trisomy 15
11. Abnormal chromosomes 14 and 15 in abortions. syndromes, and malignancy