Molecular and Cytogenetic Characterization of Two Azoospermic Patients with X-Autosome Translocation

[1] Chandley AC(1975)Cytogenetics and infertility in man I. Karyotype and seminal analysis: Results of a five-year survey of men attending a subfertility clinic. Ann. Hum Genet 39 231-254

[2] Edmond P(1981)The origin of chromosomal aberrations in man and their potential for survival and reproduction in the adult human population Ann Genet 24 5-11

[3] Christie S(2000)Human male infertility: Chromosome anomalies, meiotic disorder, abnormal spermatozoa and recurrent abortion Hum Reprod Update 6 93-105

[4] Gowans L(1997)A cytogenetic survey of 1,007 infertile males Urol Int. 58 166-176

[5] Fletcher J(1988)Meiotic analysis of two human reciprocal X-autosome translocations Cytogenet Cell Genet 48 43-47

[6] Frackiewicz A(1983)Balanced structural changes involving the human X: Effect on sexual phenotype Hum Genet 63 216-221

[7] Newton M(1995)Diverse spermatogenic defects in humans caused by Y chromosome deletions encompassing a novel RNA-binding protein gene Nat Genet 10 383-393

[8] Chandley AC(1996)Human Y chromosome azoospermia factors (AZF) mapped to different subregions in Yq11 Hum Mol Genet 5 933-943

[9] Egozcue S(2000)CFTR gene mutations and male infertility Andrologia 32 71-83

[10] Blanco J(1990)The high resolution G band of human chromosomes at 1200 band stage I Chuan Hsueh Pao 17 418-421

[1] Chandley AC(1975)Cytogenetics and infertility in man I. Karyotype and seminal analysis: Results of a five-year survey of men attending a subfertility clinic. Ann. Hum Genet 39 231-254

[2] Edmond P(1981)The origin of chromosomal aberrations in man and their potential for survival and reproduction in the adult human population Ann Genet 24 5-11

[3] Christie S(2000)Human male infertility: Chromosome anomalies, meiotic disorder, abnormal spermatozoa and recurrent abortion Hum Reprod Update 6 93-105

[4] Gowans L(1997)A cytogenetic survey of 1,007 infertile males Urol Int. 58 166-176

[5] Fletcher J(1988)Meiotic analysis of two human reciprocal X-autosome translocations Cytogenet Cell Genet 48 43-47

[6] Frackiewicz A(1983)Balanced structural changes involving the human X: Effect on sexual phenotype Hum Genet 63 216-221

[7] Newton M(1995)Diverse spermatogenic defects in humans caused by Y chromosome deletions encompassing a novel RNA-binding protein gene Nat Genet 10 383-393

[8] Chandley AC(1996)Human Y chromosome azoospermia factors (AZF) mapped to different subregions in Yq11 Hum Mol Genet 5 933-943

[9] Egozcue S(2000)CFTR gene mutations and male infertility Andrologia 32 71-83

[10] Blanco J(1990)The high resolution G band of human chromosomes at 1200 band stage I Chuan Hsueh Pao 17 418-421