Physical and mental defect of chromosomal origin in four individuals of the same family. Trisomy for the short arm of 9
- 23 April 1975
- journal article
- Published by Wiley in Clinical Genetics
- Vol. 7 (4) , 261-273
- https://doi.org/10.1111/j.1399-0004.1975.tb00328.x
Abstract
A family with the reciprocal translocation t(9;22)(q13;q11) segregating in genetically balanced and unbalanced form is identified. The clinical features of four members with trisomy for the short arm of 9, and the proximal part of the long arm of 9, are described in detail. Features in common are summarized and compared with developmental abnormality observed in other examples of trisomy for the short arm of 9. An attempt is made to delineate further the clinical features commonly seen in trisomy for the short arm of 9.Keywords
This publication has 11 references indexed in Scilit:
- A New Case of Trisomy for the Short Arm of No. 9 ChromosomeJournal of Medical Genetics, 1973
- Analyse de la trisomie 9p par dénaturation ménagéePublished by Springer Nature ,1973
- A RAPID BANDING TECHNIQUE FOR HUMAN CHROMOSOMESThe Lancet, 1971
- Partielle Trisomie C9 bei balancierter B4/C9-Translokation bei der MutterEuropean Journal of Pediatrics, 1971
- Presumed trisomy for the short arm of chromosome No. 9 not due to inherited translocationPublished by Springer Nature ,1971
- Karyotype analysis utilizing differentially stained constitutive heterochromatin of human and murine chromosomesChromosoma, 1971
- Familial transmission of a chromosomal translocation t(2q+;Cp-).Journal of Medical Genetics, 1969
- A new translocation between chromosomes in the 6-12 and 21-22 groups.Journal of Medical Genetics, 1967
- Congenital anomalies due to transmission of a chromosome translocation.Journal of Medical Genetics, 1966
- Structural heterozygosis in man: analysis of two familiesAnnals of Human Genetics, 1962