An inherited pericentric chromosomal inversion (46, inv3 [p-q+]) associated with skeletal anomalies
- 30 September 1971
- journal article
- Published by Elsevier in The Journal of Pediatrics
- Vol. 79 (3), 456-462
- https://doi.org/10.1016/s0022-3476(71)80156-7
Abstract
No abstract availableKeywords
This publication has 13 references indexed in Scilit:
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- Inherited pericentric inversion of chromosome number two: A linkage study*Annals of Human Genetics, 1969
- Strukturanomalie (inv (p-q+)?) eines Chromosoms der Gruppe C+X bei einem jungen mit multiplen dysplasien und dissoziationen der psychischen entwicklungHuman Genetics, 1969
- Pericentric inversion in a family with a 21/22 translocationCytogenetic and Genome Research, 1968
- Pericentric inversion of a group C autosome: a study of three familiesAnnals of Human Genetics, 1968
- Pericentric inversion in a group D chromosome (13?15) associated with amenorrhea and gonadal dysgenesisAnnals of Human Genetics, 1967
- CHROMOSOME STUDIES IN FIVE CASES OF COLOBOMA OF THE IRISThe Lancet, 1965
- Multiple congenital anomaliesassociated with probable pericentric inversion of chromosome No. 4 and mosaicism in an asymptomatic motherThe Journal of Pediatrics, 1964
- An Aberrant Autosome (13–15) in a Human Female and Her Father, both Apparently NormalCytogenetic and Genome Research, 1963
- Chromosome preparations of leukocytes cultured from human peripheral bloodExperimental Cell Research, 1960