Sperm chromosome analysis in the father of a child with a de-novo reciprocal translocation t(11;15)(q12;q22) by G-banding and fluorescence in-situ hybridization

By Colls P  

Human Reproduction, Vol. 13, Iss. 1, 1998-01 ,pp. : 60-64

Oxford University Press

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Unique t(Y;1)(q12;q12) reciprocal translocation with loss of the heterochromatic region of chromosome 1 in a male with azoospermia due to meiotic arrest: a case report

By Pinho Maria João  

Human Reproduction, Vol. 20, Iss. 3, 2005-03 ,pp. : 689-696

Oxford University Press

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Segregation of chromosomes in sperm of a t(X;18)(q11;p11.1) carrier inherited from his mother: Case Report

By Perrin A.   Douet-Guilbert N.   Le Bris M.J.   Keromnes G.   Langlois M.L.   Barrire P.   Amice J.   Amice V.   De Braekeleer M.   Morel F.  

Human Reproduction, Vol. 23, Iss. 1, 2008-01 ,pp. : 227-230

Oxford University Press

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Chromosome segregation in an infertile man carrying a unique pericentric inversion, inv(21)(p12q22.3), analysed using fluorescence in situ hybridization on sperm nuclei: significance for clinical genetics. A case report

By Malan V.   Pipiras E.   Sifer C.   Kanafani S.   Cedrin-Durnerin I.   Martin-Pont B.   Hugues J.N.   Wolf J.P.   Benzacken B.  

Human Reproduction, Vol. 21, Iss. 8, 2006-08 ,pp. : 2052-2056

Oxford University Press

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Case report. One normal child and a chromosomally balanced/normal twin after intracytoplasmic sperm injection in a male with a de-novo t(Y;16) translocation

By Giltay JC  

Human Reproduction, Vol. 13, Iss. 10, 1998-10 ,pp. : 2745-2747

Oxford University Press

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