MOLECULAR CYTOGENETIC CHARACTERIZATION OF
AN inv(Y)(p11.2q11.221~q11.222) IN A SYRIAN FAMILY
Al-Achkar W1,*, Wafa A1, Al-Ablog A1, Moassass F1, Liehr T2
*Corresponding Author: Professor Walid Al-Aachkar, Department of Molecular Biology and Biotechnology,
Division of Human Genetics, Atomic Energy Commission of Syria, P.O. Box 6091, Damascus, Syria; Tel.: +963-
11-213-2580; Fax: +963-11-611-2289; E-mail: ascientific@aec.org.sy
page: 73
|
|
REFERENCES
1. Bernstein R, Wadee A, Rosendorff J, Wessels
A, Jenkins T. Inverted Y chromosome polymorphism
in the Gujerati Muslim Indian population
of South Africa. Hum Genet. 1986; 74(3):
223-229.
2. Tóth A, Gaál M, László J. Familial pericentric
inversion of the Y chromosome. Ann Genet.
1984; 27(1): 60-61.
3. Motos Guirao MA. Pericentric inversion of the
human Y chromosome. An Esp Pediatr. 1989;
31(6): 583-587.
4. Shapiro LR, Pettersen RO, Wilmot PL, Warburton
D, Benn PA, Hsu LY. Pericentric inversion
of the Y chromosome and prenatal diagnosis.
Prenat Diagn. 1984; 4(6): 463-465.
5. Schmid M. Variations of content and structure of
the mammalian Y chromosome, in Sandberg AA,
Ed. The Y Chromosome, Part A, Basic Characteristics
of the Y Chromosome. New York: Alan
R. Liss. 1985: 373-401.
6. Luo YQ, Qian YL, Lu HM, Xu CM, Jin F.
Sperm-fluorescence in situ hybridization analysis
in patients with pericentric inversions of Y
chromosome. Zhonghua Yi Xue Yi Chuan Xue
Za Zhi. 2009; 26(1): 54-56.
7. Marchina E, Imperadori L, Speziani M, Omodei
U, Tombesi S, Barlati S. Chromosome abnormalities
and Yq microdeletions in infertile italian
couples referred for assisted reproductive
technique. Sex Dev. 2007; 1(6): 347-352.
8. Liehr T, Mrasek K, Weise A, Dufke A, Rodríguez
L, Martínez Guardia N, et al. Small supernumerary
marker chromosomes–progress towards
a genotype-phenotype correlation. Cytogenet
Genome Res. 2006; 112(1-2): 23-34.
9. Tomomasa H, Adachi Y, Iwabuchi M, Oshio S,
Umeda T, Iino Y, et al. Pericentric inversion of
the Y chromosome of infertile male. Arch Androl.
2000; 45(3): 181-185.
10. Causio F, Canale D, Schonauer LM, Fischetto
R, Leonetti T, Archidiacono N. Breakpoint of a
Y chromosome pericentric inversion in the DAZ
gene area. A case report. J Reprod Med. 2000;
45(7): 591-594.
11. Shaffer L, Slovak M, Cambell L, Eds. ISCN
(2009): An International System for Human Cytogenetic
Nomenclature. Basel: S. Karger, 2009.
12. Al-Achkar W, Wafa A, Liehr T, Klein E, Moassass
F. Detailed analysis of an idic(Y)(q11.21)
in a mosaic karyotype. Mol Med Report. 2012;
6(2): 293-296.
13. Jacobs PA, Hassold TJ. Chromosome abnormalities:
origin and etiology in abortions and
livebirths. In: Vogel F, Sperling K, Eds. Human
Genetics. Berlin: Springer. 1987: 233-244.
14. Hsu LY, Benn PA, Tannenbaum HL, Perlis TE,
Carlson AD. Chromosomal polymorphisms of
1, 9, 16, and Y in 4 major ethnic groups: a large
prenatal study. Am J Med Genet. 1987; 26(1):
95-101.
15. Mahajan S, Kaur A, Singh JR. Cytogenetic investigations
in mentally challenged individuals.
Int J Hum Genet. 2011; 11(2): 93-98.
16. Skaletsky H, Kuroda-Kawaguchi T, Minx PJ,
Cordum HS, Hillier L, Brown LG, et al. The
male-specific region of the human Y chromosome
is a mosaic of discrete sequence classes.
Nature. 2003; 423(6942): 825-837.
17. Knebel S, Pasantes JJ, Thi DA, Schaller F,
Schempp W. Heterogeneity of pericentric inversions
of the human y chromosome. Cytogenet
Genome Res. 2011; 132(4): 219-226.
|
|
|
|
 |
Number 27
VOL. 27 (2), 2024 |
Number 27
VOL. 27 (1), 2024 |
Number 26
Number 26 VOL. 26(2), 2023 All in one |
Number 26
VOL. 26(2), 2023 |
Number 26
VOL. 26, 2023 Supplement |
Number 26
VOL. 26(1), 2023 |
Number 25
VOL. 25(2), 2022 |
Number 25
VOL. 25 (1), 2022 |
Number 24
VOL. 24(2), 2021 |
Number 24
VOL. 24(1), 2021 |
Number 23
VOL. 23(2), 2020 |
Number 22
VOL. 22(2), 2019 |
Number 22
VOL. 22(1), 2019 |
Number 22
VOL. 22, 2019 Supplement |
Number 21
VOL. 21(2), 2018 |
Number 21
VOL. 21 (1), 2018 |
Number 21
VOL. 21, 2018 Supplement |
Number 20
VOL. 20 (2), 2017 |
Number 20
VOL. 20 (1), 2017 |
Number 19
VOL. 19 (2), 2016 |
Number 19
VOL. 19 (1), 2016 |
Number 18
VOL. 18 (2), 2015 |
Number 18
VOL. 18 (1), 2015 |
Number 17
VOL. 17 (2), 2014 |
Number 17
VOL. 17 (1), 2014 |
Number 16
VOL. 16 (2), 2013 |
Number 16
VOL. 16 (1), 2013 |
Number 15
VOL. 15 (2), 2012 |
Number 15
VOL. 15, 2012 Supplement |
Number 15
Vol. 15 (1), 2012 |
Number 14
14 - Vol. 14 (2), 2011 |
Number 14
The 9th Balkan Congress of Medical Genetics |
Number 14
14 - Vol. 14 (1), 2011 |
Number 13
Vol. 13 (2), 2010 |
Number 13
Vol.13 (1), 2010 |
Number 12
Vol.12 (2), 2009 |
Number 12
Vol.12 (1), 2009 |
Number 11
Vol.11 (2),2008 |
Number 11
Vol.11 (1),2008 |
Number 10
Vol.10 (2), 2007 |
Number 10
10 (1),2007 |
Number 9
1&2, 2006 |
Number 9
3&4, 2006 |
Number 8
1&2, 2005 |
Number 8
3&4, 2004 |
Number 7
1&2, 2004 |
Number 6
3&4, 2003 |
Number 6
1&2, 2003 |
Number 5
3&4, 2002 |
Number 5
1&2, 2002 |
Number 4
Vol.3 (4), 2000 |
Number 4
Vol.2 (4), 1999 |
Number 4
Vol.1 (4), 1998 |
Number 4
3&4, 2001 |
Number 4
1&2, 2001 |
Number 3
Vol.3 (3), 2000 |
Number 3
Vol.2 (3), 1999 |
Number 3
Vol.1 (3), 1998 |
Number 2
Vol.3(2), 2000 |
Number 2
Vol.1 (2), 1998 |
Number 2
Vol.2 (2), 1999 |
Number 1
Vol.3 (1), 2000 |
Number 1
Vol.2 (1), 1999 |
Number 1
Vol.1 (1), 1998 |
|
|
