Partial monosomy of the short arm of chromosome 9
- 1 January 1978
- journal article
- research article
- Published by Springer Nature in Human Genetics
- Vol. 44 (2) , 195-200
- https://doi.org/10.1007/bf00295414
Abstract
A 10-year-old girl with partial deletion of the short arm of chromosome 9 is reported; karyotype: 46,XX,del(9)(p22). This syndrome results in a distinctive craniofacial dysmorphism with trigonocephaly and contrasting midfacial hypoplasia. Partial monosomy 9p was the result of a paternal de novo germinal deletion in this case.This publication has 11 references indexed in Scilit:
- The deletion 9p syndrome. A 61‐year‐old man with deletion of short arm 9Clinical Genetics, 1977
- The 9p- deletion syndrome A patient with a 45,XX,-9,-15, + t(9/15) constitution due to maternal 3:l meiotic disjunctionClinical Genetics, 1977
- [9p syndrome. Deletion of the short arm of chromosome 9; Monosomy of short arm 9].1977
- A case of 9p- syndromeHuman Genetics, 1977
- PARTIAL DELETION OF SHORT ARM OF CHROMOSOME-91976
- 9P- SYNDROME1976
- The 9p--syndrome.1976
- Deletion in the short arm of chromosome 9 from a subject with congenital cerebral maldevelopmentCytogenetic and Genome Research, 1976
- The 9p‐ deletion syndrome. Report of a patient with a 46, XX, 9p‐ constitution due to a paternal t(9p‐; 15q+) translocationClinical Genetics, 1975
- Deletion of the short arm of chromosome no.9 (46,9p-): a new deletion syndrome.1973