1
|
Song SH, Chiba K, Ramasamy R and Lamb DJ:
Recent advances in the genetics of testicular failure. Asian J
Androl. 18:350–355. 2016. View Article : Google Scholar : PubMed/NCBI
|
2
|
Codina-Pascual M, Oliver-Bonet M, Navarro
J, Starke H, Liehr T, Gutiérrez-Mateo C, Sánchez-García JF, Arango
O, Egozcue J and Benet J: FISH characterization of a dicentric Yq
(p11.32) isochromosome in an azoospermic male. Am J Med Genet.
127A:302–306. 2004. View Article : Google Scholar : PubMed/NCBI
|
3
|
Lehmann KJ, Kovac JR, Xu J and Fischer MA:
Isodicentric Yq mosaicism presenting as infertility and maturation
arrest without altered SRY and AZF regions. J Assist Reprod Genet.
29:939–942. 2012. View Article : Google Scholar : PubMed/NCBI
|
4
|
Lee BY, Kim SY, Park JY, Choi EY, Kim DJ,
Kim JW, Ryu HM, Cho YH, Park SY and Seo JT: Unusual maternal
uniparental isodisomic × chromosome mosaicism with asymmetric y
chromosomal rearrangement. Cytogenet Genome Res. 142:79–86. 2014.
View Article : Google Scholar : PubMed/NCBI
|
5
|
Tuck-Muller CM, Chen H, Martínez JE, Shen
CC, Li S, Kusyk C, Kusyk C, Batista DA, Bhatnagar YM, Dowling E and
Wertelecki W: Isodicentric Y chromosome: Cytogenetic, molecular and
clinical studies and review of the literature. Hum Genet.
96:119–129. 1995. View Article : Google Scholar : PubMed/NCBI
|
6
|
Kalantari H, Asia S, Totonchi M,
Vazirinasab H, Mansouri Z, Moradi S Zarei, Haratian K, Gourabi H
and Meybodi A Mohseni: Delineating the association between
isodicentric chromosome Y and infertility: A retrospective study.
Fertil Steril. 101:1091–1096. 2014. View Article : Google Scholar : PubMed/NCBI
|
7
|
Vogt PH, Edelmann A, Hirschmann P and
Köhler MR: The azoospermia factor (AZF) of the human Y chromosome
in Yq11: Function and analysis in spermatogenesis. Reprod Fertil
Dev. 7:685–693. 1995. View Article : Google Scholar : PubMed/NCBI
|
8
|
Dong Y, Du RC, Jiang YT, Wu J, Li LL and
Liu RZ: Impact of chromosomal translocations on male infertility,
semen quality, testicular volume and reproductive hormone levels. J
Int Med Res. 40:2274–2283. 2012. View Article : Google Scholar : PubMed/NCBI
|
9
|
Luo B, Li W, Deng CH, Zheng FF, Sun XZ,
Wang DH and Dai YP: Utility of fluorescence in situ hybridization
in the diagnosis of upper urinary tract urothelial carcinoma.
Cancer Genet Cytogenet. 189:93–97. 2009. View Article : Google Scholar : PubMed/NCBI
|
10
|
Totonchi M, Meybodi A Mohseni, Boroujeni P
Borjian, Gilani M Sedighi, Almadani N and Gourabi H: Clinical data
for 185 infertile Iranian men with Y-chromosome microdeletion. J
Assist Reprod Genet. 29:847–853. 2012. View Article : Google Scholar : PubMed/NCBI
|
11
|
Al-Achkar W, Moassass F, Al-Halabi B and
Al-Ablog A: Mutations of the Connexin 26 gene in families with
non-syndromic hearing loss. Mol Med Rep. 4:331–335. 2011.
View Article : Google Scholar : PubMed/NCBI
|
12
|
Wang X, Wang XR, Liu MG, Wang Q and Liu
JY: Genetic analysis of a family with 46,XY ‘female’ associated
with infertility. Yi Chuan Xue Bao. 33:19–25. 2006.PubMed/NCBI
|
13
|
Hou Y, Fan W, Yan L, Li R, Lian Y, Huang
J, Li J, Xu L, Tang F, Xie XS and Qiao J: Genome analyses of single
human oocytes. Cell. 155:1492–1506. 2013. View Article : Google Scholar : PubMed/NCBI
|
14
|
Meng MV, Cha I, Ljung BM and Turek PJ:
Relationship between classic histological pattern and sperm
findings on fine needle aspiration map in infertile men. Hum
Reprod. 15:1973–1977. 2000. View Article : Google Scholar : PubMed/NCBI
|
15
|
Foresta C, Moro E and Ferlin A: Y
chromosome microdeletions and alterations of spermatogenesis.
Endocr Rev. 22:226–239. 2001. View Article : Google Scholar : PubMed/NCBI
|
16
|
Hsu LF: Phenotype/karyotype correlations
of Y chromosome aneuploidy with emphasis on structural aberrations
in postnatally diagnosed cases. Am J Med Genet. 53:108–140. 1994.
View Article : Google Scholar : PubMed/NCBI
|
17
|
Oliveira RM, Verreschi IT, Lipay MV, Eça
LP, Guedes AD and Bianco B: Y chromosome in Turner syndrome: Review
of the literature. Sao Paulo Med J. 127:373–378. 2009. View Article : Google Scholar : PubMed/NCBI
|
18
|
Antonelli A, Marcucci L, Elli R, Tanzi N,
Paoli D, Radicioni A, Lombardo F, Lenzi A and Gandini L: Semen
quality in men with Y chromosome aberrations. Int J Androl.
34:453–460. 2011. View Article : Google Scholar : PubMed/NCBI
|
19
|
Lange J, Skaletsky H, van Daalen SK, Embry
SL, Korver CM, Brown LG, Oates RD, Silber S, Repping S and Page DC:
Isodicentric Y chromosomes and sex disorders as byproducts of
homologous recombination that maintains palindromes. Cell.
138:855–869. 2009. View Article : Google Scholar : PubMed/NCBI
|
20
|
Geng Q, Luo FW, Wu WQ, Xu ZY, Wang L, Wang
Q and Xie JS: Cytogenetic and molecular analysis of idic(Yp) in 1
infertile man and 1 prenatal fetus. Zhonghua Nan Ke Xue.
19:642–646. 2013.(In Chinese). PubMed/NCBI
|
21
|
Haaf T and Schmid M: Y isochromosome
associated with a mosaic karyotype and inactivation of the
centromere. Hum Genet. 85:486–490. 1990. View Article : Google Scholar : PubMed/NCBI
|
22
|
Mićić M, Mićić S, Babić M and Diklić V:
Phenotype of two males with abnormal Y chromosomes. Clin Genet.
37:321–326. 1990. View Article : Google Scholar : PubMed/NCBI
|
23
|
Odorisio T, Rodriguez TA, Evans EP, Clarke
AR and Burgoyne PS: The meiotic checkpoint monitoring synapsis
eliminates spermatocytes via p53-independent apoptosis. Nat Genet.
18:257–261. 1998. View Article : Google Scholar : PubMed/NCBI
|
24
|
Layman LC, Tho SP, Clark AD, Kulharya A
and McDonough PG: Phenotypic spectrum of 45,X/46,XY males with a
ring Y chromosome and bilaterally descended testes. Fertil Steril.
91:791–797. 2009. View Article : Google Scholar : PubMed/NCBI
|
25
|
Yang XG, Li YP, Ma GS, Hu XQ, Wang JZ, Cui
ZH, Wang ZH, Yu WT, Yang ZX and Zhai FY: Study on weight and height
of the Chinese people and the differences between 1992 and 2002.
Zhonghua Liu Xing Bing Xue Za Zhi. 26:489–493. 2005.(In Chinese).
PubMed/NCBI
|
26
|
Lin YH, Lin YM, Lin YH, Chuang L, Wu SY
and Kou PL: Ring (Y) in two azoospermic men. Am J Med Genet A.
128A:209–213. 2004. View Article : Google Scholar : PubMed/NCBI
|
27
|
Rao E, Weiss B, Fukami M, Rump A, Niesler
B, Mertz A, Muroya K, Binder G, Kirsch S, Winkelmann M, et al:
Pseudoautosomal deletions encompassing a novel homeobox gene cause
growth failure in idiopathic short stature and Turner syndrome. Nat
Genet. 16:54–63. 1997. View Article : Google Scholar : PubMed/NCBI
|
28
|
Guevarra FM, Nimkarn S, New MI and Lin-Su
K: Long-term growth hormone therapy in an adolescent boy with
45,X/46,XidicY(p11). J Pediatr. 155:752–755. 2009. View Article : Google Scholar : PubMed/NCBI
|
29
|
Wu HH, Lee TH, Chen CD, Yeh KT and Chen M:
Delineation of an isodicentric Y chromosome in a mosiac
45,X/46,X,idic(Y)(qter-p11.3::p11.3-qter) fetus bySRY sequencing,
G-banding, FISH, SKY and study of distribution in different
tissues. J Formos Med Assoc. 106:403–410. 2007. View Article : Google Scholar : PubMed/NCBI
|