Localization of factors controlling spermatogenesis in the nonfluorescent portion of the human y chromosome long arm
- 1 January 1976
- journal article
- research article
- Published by Springer Nature in Human Genetics
- Vol. 34 (2) , 119-124
- https://doi.org/10.1007/bf00278879
Abstract
A deletion of the Y chromosome at the distal portion of band q11 was found in 6 men with normal male habitus but with azoospermia. Five of them were found during a survey of 1170 subfertile males while the sixth was karyotyped because of slight bone abnormalities. These findings, together with a review of the literature, suggest that on the distal portion of the nonfluorescent segment of the long arm of the Y, factors are located controlling spermatogenesis.This publication has 28 references indexed in Scilit:
- Translocations causing non-fluorescent Y chromosomes in human XO/XY mosaicsHereditas, 2009
- Chromosome polymorphism in a human newborn populationCytogenetic and Genome Research, 1975
- Deletion of the long arms of the Y chromosome with normal male development and intelligenceJournal of Medical Genetics, 1974
- PROBABLE LONG-ARM DELETION OF Y CHROMOSOME IN BOY OF SHORT STATUREThe Lancet, 1973
- Localization of male determining factor on short arm of Y chromosome Case report of a baby with 46, x, t (Yp+;14q‐)Clinical Genetics, 1972
- Quinacrine Fluorescence of the Human Y ChromosomeNature, 1971
- Meiotic studies on a subfertile patient with a ring Y chromosomeCytogenetic and Genome Research, 1971
- Structural Abnormalities of the Y Chromosome in ManNature, 1966
- A mentally retarded boy with a minute Y chromosomeThe Journal of Pediatrics, 1965
- Deletion of Y Chromosome in a Family with Muscular Dystrophy and HypospadiasBMJ, 1962