X-Y CHROMOSOMAL INTERCHANGE IN THE ÆTIOLOGY OF TRUE HERMAPHRODITISM AND OF XX KLINEFELTER'S SYNDROME
- 1 August 1966
- journal article
- research article
- Published by Elsevier in The Lancet
- Vol. 288 (7461) , 475-476
- https://doi.org/10.1016/s0140-6736(66)92778-4
Abstract
No abstract availableThis publication has 11 references indexed in Scilit:
- THE CHROMOSOME CONSTITUTION OF A HUMAN PHENOTYPIC INTERSEX: RECONFIRMATION OF A 46-CHROMOSOME, XX, APPARENTLY NON-MOSAIC “TRUE HERMAPHRODITE”Hereditas, 2009
- Structural Abnormalities of the Y Chromosome in ManNature, 1966
- TWO MALES WITH FEMALE CHROMOSOMESActa Endocrinologica, 1965
- Karyotype-phenotype Correlations in Gonadal Dysgenesis and Their Bearing on the Pathogenesis of MalformationsJournal of Medical Genetics, 1965
- MIXED GONADAL DYSGENESIS WITH XX/XY MOSAICISM: The Evidence for the Occurrence of Fertilisation by Two Spermatozoa in ManThe Lancet, 1965
- Chromosomal Analysis of Multiple Tissues from a True HermaphroditeJournal of Clinical Endocrinology & Metabolism, 1964
- Familial True HermaphrodismJournal of Clinical Endocrinology & Metabolism, 1963
- Gene Action in the X-chromosome of the Mouse (Mus musculus L.)Nature, 1961
- THE CHROMOSOME COMPLEMENT IN TRUE HERMAPHRODITISMThe Lancet, 1960
- A Presumptive Human XXY/XX MosaicNature, 1959