A girl with partial long-arm deletion of chromosome 11 and familial pericentric inversion of chromosome 9
- 1 January 1977
- journal article
- research article
- Published by Springer Nature in Human Genetics
- Vol. 36 (1), 117-122
- https://doi.org/10.1007/bf00390443
Abstract
A girl with 46, XX, del (11) (q23), inv (9) (p13,q13) is described. The patient shows many dysplastic signs mainly of the face and skull. The pericentric inversion of chromosome 9 has been inherited from the mother (46, XX, inv (9) (p13,q13)).Keywords
This publication has 11 references indexed in Scilit:
- A case with 46, XX, del (11) (q21)Clinical Genetics, 2008
- Chromosome 11 long arm partial deletion: a new syndrome.1976
- Deletion of 11q: report of two cases and a review.1976
- [Partial 11q monosomy and trigonocephaly. A new syndrome].1975
- Anomalies associated with partial deletion of long arm of chromosome 11The Journal of Pediatrics, 1975
- Association of pericentric inversion of chromosome 9 and reproductive failure in ten unrelated familiesPublished by Springer Nature ,1975
- Incidence of chromosome aberrations among 11 148 newborn childrenPublished by Springer Nature ,1975
- Structural variation in chromosome No 9.1974
- Pericentric Inversion of Chromosome 9Nature New Biology, 1973
- An (11;21) Translocation in Four Generations with Chromosome 11 Abnormalities in the OffspringHuman Heredity, 1973