Full trisomy 7 and Potter syndrome
- 1 April 1980
- journal article
- research article
- Published by Springer Nature in Human Genetics
- Vol. 54 (1), 13-18
- https://doi.org/10.1007/bf00279043
Abstract
A patient with typical Potter's syndrome and full trisomy 7 is described. All previous reports on chromosome 7 abnormalities, whether monosomic or trisomic, p or q, are reviewed and discussed, establishing two 7q trisomy snydromes: 7q22→7q31 and 7q22, q31→7qter. Some implications of the finding of full trisomy 7 in a case of Potter's syndrome are discussed.Keywords
This publication has 28 references indexed in Scilit:
- Partial trisomy of the long arm of chromosome 7Clinical Genetics, 2008
- Meiotic analysis of a pericentric inversion, inv(7) (p22q32), in the father of a child with a duplication-deletion of chromosome 7Cytogenetic and Genome Research, 1978
- 7q deletion syndrome (7q32→7qter)Clinical Genetics, 1977
- A partial long arm deletion of chromosome 7:46,XY,del(7)(q32).Journal of Medical Genetics, 1977
- Interstitial deletion of the long arm of chromosome no. 7 (7q‐) in an infant with multiple anomaliesClinical Genetics, 1976
- Two different chromosome abnormalities resulting from a translocation carrier fatherThe Journal of Pediatrics, 1973
- Deletion of the long arm of chromosome no. 7: Tentative assignment of the Kidd (Jk) LocusClinical Genetics, 1973
- Partial Trisomy of the Long Arm of Chromosome No. 7Journal of Medical Genetics, 1973
- Ring chromosome 7 with variable phenotypic expressionCytogenetic and Genome Research, 1973
- Chromosome survey of a hospital for the mentally subnormal Part 2: Autosome abnormalitiesClinical Genetics, 1972