Literature DB >> 10821218

Clinical, cytogenetic and molecular analysis of three 46,XX males.

E Plöchl1, I Vlasak, O Rittinger, E Bergendi, M Stopar, P Kurnik, M Nachtigall, H Zierler, G A Rappold, K Schiebel.   

Abstract

Cytogenetic analysis, fluorescent in situ hybridization (FISH) and polymerase chain reaction (PCR) were applied to characterize the Y-chromosomal breakpoints of three XX male patients. Two of these patients show a breakpoint within a protein kinase gene, PRKY, previously described as a hotspot of ectopic recombination between homologous regions on X and Y chromosomes during male meiosis. The slightly different clinical phenotypes of the three patients cannot be correlated with the localization of the breakpoints.

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Year:  1999        PMID: 10821218     DOI: 10.1515/jpem.1999.12.3.389

Source DB:  PubMed          Journal:  J Pediatr Endocrinol Metab        ISSN: 0334-018X            Impact factor:   1.634


  1 in total

1.  Cytogenetic Investigation in a Group of Ten Infertile Men with Non-Obstructive Azoospermia: First Algerian 46, XX Syndrome.

Authors:  Meriem Baziz; Zohra Hamouli-Said; Ilham Ratbi; Mohamed Habel; Soukaina Guaoua; Aziza Sbiti; Abdelaziz Sefiani
Journal:  Iran J Public Health       Date:  2016-06       Impact factor: 1.429

  1 in total

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