Spectral karyotyping and fluorescencein situ hybridization analysis ofde novo partial duplication of Yq (Yq11.2→qter) and partial monosomy 5p (5p15.3→pter)

2005 ◽  
Vol 25 (8) ◽  
pp. 723-725 ◽  
Author(s):  
Chih-Ping Chen ◽  
Shuan-Pei Lin ◽  
Chyi-Chyang Lin ◽  
Yueh-Chun Li ◽  
Lie-Jiau Hsieh ◽  
...  
Keyword(s):  
Hybridization Analysis ◽  
Fluorescencein Situ Hybridization ◽  
Spectral Karyotyping ◽  
Partial Monosomy ◽  
Partial Duplication ◽  
Partial Monosomy 5P

45, X Constitution in a H-Y antigen positive boy with partial monosomy 5p

2008 ◽  
Vol 19 (4) ◽  
pp. 290-297 ◽  
Author(s):  
H. Seidel ◽  
K. Miller ◽  
M. Spoljars ◽  
S. Stengel-Rutkowski
Keyword(s):  
Partial Monosomy ◽  
Partial Monosomy 5P

Familial partial monosomy 5p and trisomy 5q; three cases due to paternal pericentric inversion 5 (p151q333)

2008 ◽  
Vol 26 (3) ◽  
pp. 209-215 ◽  
Author(s):  
F. A. Beemer ◽  
H. F. de France ◽  
I. J. M. Rosina-Angelista ◽  
L. J. Gerards ◽  
B. P. Cats ◽  
...  
Keyword(s):  
Pericentric Inversion ◽  
Partial Monosomy ◽  
Partial Monosomy 5P

scholarly journals Partial monosomy 5p and partial trisomy 5q due to paternal pericentric inversion of chromosome 5

1993 ◽  
Vol 38 (3) ◽  
pp. 319-328 ◽  
Author(s):  
Kazuhiro Ono ◽  
Yasushi Ohashi ◽  
Hisashi Nakano ◽  
Hirosuke Togashi ◽  
Yoji Kannari ◽  
...  
Keyword(s):  
Pericentric Inversion ◽  
Partial Trisomy ◽  
Chromosome 5 ◽  
Partial Monosomy ◽  
Partial Monosomy 5P ◽  
Partial Trisomy 5Q

scholarly journals Partial monosomy 5p and partial trisomy 5q due to paternal pericentric inversion 5(p15.1q35.1)

1989 ◽  
Vol 34 (2) ◽  
pp. 129-134 ◽  
Author(s):  
Tohru Sonoda ◽  
Kenji Kawaguchi ◽  
Ken-ichi Ohba ◽  
Harumichi Madokoro ◽  
Shozo Ohdo
Keyword(s):  
Pericentric Inversion ◽  
Partial Trisomy ◽  
Partial Monosomy ◽  
Partial Monosomy 5P ◽  
Partial Trisomy 5Q

Dual-colour fluorescencein situ hybridization analysis of synovial sarcoma

1998 ◽  
Vol 184 (1) ◽  
pp. 7-13 ◽  
Author(s):  
Peng Yang ◽  
Takanori Hirose ◽  
Tadashi Hasegawa ◽  
Kazuo Hizawa ◽  
Toshiaki Sano
Keyword(s):  
Synovial Sarcoma ◽  
Hybridization Analysis ◽  
Fluorescencein Situ Hybridization ◽  
Dual Colour

Familial Translocation t(5;15)(p14.2;q26.2) Causing a Mirror Combination of Several Known Genetic Conditions

2017 ◽  
Vol 15 (06) ◽  
pp. 332-337
Author(s):  
Yael Goldberg ◽  
Racheli Berger ◽  
Amir Peleg ◽  
Lena Sagi-Dain
Keyword(s):  
Clinical Features ◽  
Partial Trisomy ◽  
Balanced Translocation ◽  
Partial Monosomy ◽  
Familial Translocation ◽  
Partial Monosomy 5P

AbstractTwo siblings with an unbalanced cytogenetic composition are described: a brother with partial trisomy 5p and distal 15q microdeletion, and a sister with partial monosomy 5p and distal 15q microduplication, resulting from a familial balanced translocation 46,XY; t(5;15)(p14.2;q26.2). To our best knowledge, there are no previous clinical and cytogenetic reports in the literature describing a family with concomitant presence of such a unique mirror combination. Clinical features of pure imbalances and the effects of their combination are discussed.

Fluorescencein situ hybridization analysis of chromosome 12 anomalies in semen cells from patients with carcinomain situ of the testis

1998 ◽  
Vol 186 (3) ◽  
pp. 235-239 ◽  
Author(s):  
Fan Jing Meng, ◽  
Yue Zhou ◽  
Aleksander Giwercman ◽  
Niels E. Skakkebaek ◽  
Ad Geurts Van Kessel ◽  
...  
Keyword(s):  
Hybridization Analysis ◽  
Chromosome 12 ◽  
Fluorescencein Situ Hybridization ◽  
Carcinomain Situ
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