Aspermia, associated with a presumably balanced X/autosomal translocation

1976 ◽  
Vol 31 (1) ◽  
pp. 97-106 ◽  
Author(s):  
S. Stengel-Rutkowski ◽  
H. Zankl ◽  
A. Rodewald ◽  
S. Scharrer ◽  
J. P. Chaudhuri ◽  
...  
1972 ◽  
Vol 14 (2) ◽  
pp. 133-136 ◽  
Author(s):  
Sabine Fr�nd ◽  
Thea Koske-Westphal ◽  
Sigrun Fuchs-Mecke ◽  
Eberhard Passarge

1970 ◽  
Vol 7 (4) ◽  
pp. 402-406 ◽  
Author(s):  
M J Thorburn ◽  
P A Martin ◽  
U N Pathak

2008 ◽  
Vol 53 (4) ◽  
pp. 293-297 ◽  
Author(s):  
Thomas Eggermann ◽  
Ulrike Mau ◽  
Ute Klein-Vogler ◽  
Heidemarie Kendziorra ◽  
Susanne Mackensen-Haen ◽  
...  

1996 ◽  
Vol 6 (4) ◽  
pp. 201-208 ◽  
Author(s):  
L. He ◽  
A. Carothers ◽  
D. H.R. Blackwood ◽  
P. Teague ◽  
A. W. Maclean ◽  
...  

Author(s):  
R. J McKinlay Gardner ◽  
David J Amor

The sex chromosomes (gonosomes) are different, and sex chromosome translocations need to be considered separately from translocations between autosomes. A sex chromosome can engage in translocation with an autosome, with the other sex chromosome, or even with its homolog. The qualities of the sex chromosomes have unique implications in terms of the genetic functioning of gonosome-autosome translocations. This chapter acknowledges the specific peculiarities that the sex chromosomes imply: the X being subject to transcriptional silencing; and the very small Y gene complement being confined largely to sex-determining loci. It reviews translocations between sex chromosomes and autosomes; between X and Y chromosomes; and even the very rare circumstance of between X chromosomes and between Y chromosomes. The differences in assessing risk, according to chromosome form, in comparison with the autosomal translocation, are reviewed, and the biology behind these differences is discussed.


2019 ◽  
Vol 10 ◽  
Author(s):  
Malorie P. Baily ◽  
Felipe Avila ◽  
Pranab J. Das ◽  
Michelle A. Kutzler ◽  
Terje Raudsepp

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