Pericentric enversion of chromosome no. 13 in a large family leading to duplication deficiency causing congenital malformations in three individuals.
Open Access
- 1 December 1972
- journal article
- research article
- Published by BMJ in Journal of Medical Genetics
- Vol. 9 (4), 413-421
- https://doi.org/10.1136/jmg.9.4.413
Abstract
No abstract availableThis publication has 9 references indexed in Scilit:
- Patau's syndrome with D1 duplication-deficiency derived from a maternal D group pericentric inversionAnnals of Human Genetics, 1971
- Identification of G group anomalies in Down's syndrome by quinacrine dihydrochloride fluorescence stainingHuman Genetics, 1971
- Pericentric inversion of a number 15 chromosome in nine members of one familyCytogenetic and Genome Research, 1970
- Pericentric inversion in a group D chromosome (13?15) associated with amenorrhea and gonadal dysgenesisAnnals of Human Genetics, 1967
- Human meiosis: the occurrence of interlocked bivalents in a normal maleAnnals of Human Genetics, 1966
- Cerebral Gigantism in ChildhoodNew England Journal of Medicine, 1964
- The D1 trisomy syndromeThe Journal of Pediatrics, 1963
- An Aberrant Autosome (13–15) in a Human Female and Her Father, both Apparently NormalCytogenetic and Genome Research, 1963
- Chromosome Analysis from Capillary BloodCytogenetic and Genome Research, 1962