CASE OF PARTIAL 9P MONOSOMY WITH SOME UNUSUAL CLINICAL FEATURES
- 1 January 1978
- journal article
- research article
- Vol. 21 (1) , 51-55
Abstract
A patient is described with a karyotype 46,XX,del(9)(qter .fwdarw. p22:) and having the main clinical characteristics of the pure monosomy for part of the short arm of chromosome No. 9, among which craniosynostosis and trigonocephaly. She also has a few atypical features: a clearly advanced osseous maturation, marked congenital vertebral anomalies and unusual dermatoglyphics.This publication has 7 references indexed in Scilit:
- ANOTHER CASE OF 9P-SYNDROME1978
- 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
- A case of 9p- syndromeHuman Genetics, 1977
- 9P- SYNDROME1976
- CT banding of human chromosomesHuman Genetics, 1976
- Deletion in the short arm of chromosome 9 from a subject with congenital cerebral maldevelopmentCytogenetic and Genome Research, 1976