Clinicopathological study in a female infant with 46,XX,i(18q) showing mixed features of both trisomy 18 and monosomy 18p
- 1 September 1985
- journal article
- research article
- Published by Springer Nature in Journal of Human Genetics
- Vol. 30 (3) , 219-226
- https://doi.org/10.1007/bf01876472
Abstract
No abstract availableKeywords
This publication has 10 references indexed in Scilit:
- Isochromosome 18q with karyotype 46, XX, i(18q). Cytogenetics and pathologyClinical Genetics, 1984
- Trisomy 18 phenotype in a patient with an isopseudodicentric 18 chromosome.Journal of Medical Genetics, 1984
- A CASE OF EDWARDS SYNDROME WITH PSEUDODICENTRIC ISOCHROMOSOME-18 - 46,XY,I DIC(18)(P11-P11)1982
- Abnormal neuronal development in the visual cortex of the human fetus and infant with down's syndrome. A quantitative and qualitative golgi studyBrain Research, 1981
- Features of trisomy 18 and 18p-syndromes in an infant with 46, XY, i(18q)Clinical Genetics, 1979
- 18p− syndrome associated with hemivertebrae, fused ribs and micropenisJournal of Human Genetics, 1977
- Structural organization of the cerebral cortex (motor area) in human chromosomal aberrations. A golgi study. I. D1 (13–15) trisomy, patau syndromeBrain Research, 1974
- Structural abnormalities of the cerebral cortex in human chromosomal aberrations: a Golgi studyBrain Research, 1972
- Central nervous system abnormalities in Trisomy E (17–18) syndromeJournal of the Neurological Sciences, 1972
- BRAIN MALFORMATIONS IN THE TRISOMY 18 SYNDROMEBrain, 1970