scholarly journals Ring chromosome 12 and severe oligospermia: a case report

2008 ◽  
Vol 90 (2) ◽  
pp. 443.e13-443.e15 ◽  
Author(s):  
J. Ryan Martin ◽  
Anne Wold ◽  
Hugh S. Taylor
1993 ◽  
Vol 8 (2) ◽  
pp. 69-73 ◽  
Author(s):  
Jeffrey R. Sawyer ◽  
Gael Sammartino ◽  
M. Husain ◽  
Jane M. Lewis ◽  
Bruce Anderson ◽  
...  

1982 ◽  
Vol 12 (1) ◽  
pp. 109-114 ◽  
Author(s):  
Yoshikazu Nishi ◽  
Osamu Yoshimura ◽  
Koso Ohama ◽  
Tomofusa Usui ◽  
John M. Opitz

2013 ◽  
Vol 161 (6) ◽  
pp. 1447-1452 ◽  
Author(s):  
Else la Cour Sibbesen ◽  
Cathrine Jespersgaard ◽  
Daniela Alosi ◽  
Anne-Marie Bisgaard ◽  
Zeynep Tümer

2015 ◽  
Vol 5 (1) ◽  
pp. 123-128
Author(s):  
Maurício Rodrigues ◽  
Renata Moreira ◽  
Patrícia Ribeiro

2005 ◽  
Vol 14 (3) ◽  
pp. 141-143 ◽  
Author(s):  
P.R.G. Zen ◽  
L.L.C. Pinto ◽  
C. Graziadio ◽  
V.B. Pereira ◽  
G.A. Paskulin

1980 ◽  
Vol 5 (2) ◽  
pp. 165-170 ◽  
Author(s):  
Nina Scribanu ◽  
Eva B. McCullars ◽  
Robert C. Baumiller ◽  
Angel R. Colon ◽  
Celia J. Kaye

2019 ◽  
Vol 9 (3) ◽  
pp. 351-353
Author(s):  
Sajjadian Negar*, Herman Moghadam Kambiz

Background: Ring Chromosome 18 is a rare chromosomal disorder with loss of geneticmaterial from one or both ends of the 18th chromosome and fusion of the chromosomalends to form a ring. Associated symptoms and physical features may beextremely variable.Case report: we observed a 2.5 year old girl with the features typical for r(18)carriers additionally manifested a Tetralogy of fallot. Chromosomal analysis on thebasis of G-banding technique was performed. Chromosomal investigation appeared as46, XY,r(18) (p11.31q22.3).Conclusion: This information may help healthcare team make diagnosis a personwith ring 18.


Author(s):  
Selda ŞİMŞEK ◽  
Diclehan ORAL ◽  
İ̇lyas YÜCEL

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