Literature DB >> 8501188

Chromosome studies in in-vitro fertilization patients.

R Lange1, G Johannson, W Engel.   

Abstract

Human fertility problems may be due to chromosomal aberrations in one or both partners. In couples asking for in-vitro fertilization (IVF) the question arises as to whether chromosomal analysis is necessary. We analysed the karyotypes of 72 couples attending our clinic for IVF. Normal chromosomes were found in 131 individuals. One male was found to be a carrier of a Robertsonian translocation t(14q;21q), a second male had a reciprocal translocation t(2;4)(q14;p15) and 11 females exhibited sex chromosome mosaicism. A single cell aberration was demonstrated in 26% (38/144) of all individuals studied. These results clearly show that chromosomal analysis should be performed in couples asking for IVF.

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Year:  1993        PMID: 8501188     DOI: 10.1093/oxfordjournals.humrep.a138098

Source DB:  PubMed          Journal:  Hum Reprod        ISSN: 0268-1161            Impact factor:   6.918


  2 in total

1.  A meta-analysis of controlled studies comparing major malformation rates in IVF and ICSI infants with naturally conceived children.

Authors:  Alfred A Rimm; Alyce C Katayama; Mireya Diaz; K Paul Katayama
Journal:  J Assist Reprod Genet       Date:  2004-12       Impact factor: 3.412

2.  Report of trisomy 2q34-qter and monosomy 4q35.2-qter in a child with mild dysmorphic syndrome and karyotype 46,XY,der(4)t(2;4)(q34;q35.2)pat.

Authors:  Juan Pablo Meza-Espinoza; Enrique Sáinz González; Christian J N León-León; Eliakym Arámbula-Meraz; José Alfredo Contreras-Gutiérrez; Noemí García-Magallanes; Jesús Madueña-Molina; Fred Luque-Ortega; Salvador Cervín-Serrano; Verónica Judith Picos-Cárdenas
Journal:  Mol Cytogenet       Date:  2020-05-19       Impact factor: 2.009

  2 in total

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