Preferential alternate segregation in the common t(11;22)(q23;q11) reciprocal translocation: sperm FISH analysis in two brothers (Q81318818)

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7 January 2020

title

Preferential alternate segregation in the common t(11;22)(q23;q11) reciprocal translocation: sperm FISH analysis in two brothers (English)

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7 January 2020

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7 January 2020

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7 January 2020

Josep Egozcue i Cuixart

series ordinal

object named as

Josep Egozcue

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7 January 2020

Ester Anton

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7 January 2020

publication date

1 December 2004

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Reproductive BioMedicine Online

7 January 2020

published in

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7 January 2020

volume

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issue

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7 January 2020

page(s)

637-644

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Evaluation of segregation patterns of 21;21 Robertsonian translocation along with sex chromosomes and interchromosomal effects in sperm nuclei of carrier by FISH technique

7 January 2020

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Interchromosomal effect leading to an increase in aneuploidy in sperm nuclei in a man heterozygous for pericentric inversion (inv 9) and C-heterochromatin

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Sperm FISH studies in seven male carriers of Robertsonian translocation t(13;14)(q10;q10).

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Meiotic studies of a human male carrier of the common translocation, t(11;22), suggests postzygotic selection rather than preferential 3:1 MI segregation as the cause of liveborn offspring with an unbalanced translocation.

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Systematic analysis of 95 reciprocal translocations of autosomes

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Infertile spermatozoa in a human carrier of robertsonian translocation 14;22.

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10, 15 reciprocal translocation in an infertile man: ultrastructural and fluorescence in-situ hybridization sperm study: Case report

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Incidence of chromosome 21 disomy in human spermatozoa as determined by fluorescent in-situ hybridization

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Increased incidence of disomic sperm nuclei in a 47,XYY male assessed by fluorescent in situ hybridization (FISH).

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FISH on sperm heads allows the analysis of chromosome segregation and interchromosomal effects in carriers of structural rearrangements: results in a translocation carrier, t(5;8)(q33;q13).

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Chromosome 21 disomy in the spermatozoa of the fathers of children with trisomy 21, in a population with a high prevalence of Down syndrome: increased incidence in cases of paternal origin.

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Interchromosomal effects for chromosome 21 in carriers of structural chromosome reorganizations determined by fluorescence in situ hybridization on sperm nuclei

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A collaborative study of the segregation of inherited chromosome structural rearrangements in 1356 prenatal diagnoses

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Cytogenetic analysis of sperm chromosomes and sperm nuclei in a male heterozygous for a reciprocal translocation t(5;7)(q21;q32) by in situ hybridisation

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7 January 2021

Risks of unbalanced progeny at amniocentesis to carriers of chromosome rearrangements: data from United States and Canadian laboratories

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Analysis of chromosome abnormalities in sperm and embryos from two 45,XY,t(13;14)(q10;q10) carriers

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The segregation of a translocation t(1;4) in two male carriers heterozygous for the translocation

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Meiotic products of two reciprocal translocations studied by multicolor fluorescence in situ hybridization

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Multicolor fluorescence in situ hybridization analysis of the spermatozoa of a male heterozygous for a reciprocal translocation t(11;22)(q23;q11)

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7 January 2021

Is there an interchromosomal effect in reciprocal translocation carriers? Sperm FISH studies

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7 January 2021

Embryo development characteristics in Robertsonian and reciprocal translocations: a comparison of results with non-translocation cases

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7 January 2021

The 11q;22q translocation: a European collaborative analysis of 43 cases

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Assisting reproduction of infertile men carrying a Robertsonian translocation

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Meiotic association between the XY chromosomes and the autosomal quadrivalent of a reciprocal translocation in two infertile men, 46,XY,t(19;22) and 46,XY,t(17;21)

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7 January 2021

Possible interchromosomal effect in embryos generated by gametes from translocation carriers

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7 January 2021

Sperm analysis in a subfertile male with a Y;16 translocation, using four-color FISH

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7 January 2021

Three dimensional reconstruction of human pachytene spermatocyte nuclei of a 17;21 reciprocal translocation carrier: study of XY-autosome relationships

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7 January 2021

Analysis of segregation and aneuploidy in two reciprocal translocation carriers, t(3;9)(q26.2;q32) and t(3;9)(p25;q32), by triple-color fluorescence in situ hybridization

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7 January 2021

The 11q;22q translocation: a collaborative study of 20 new cases and analysis of 110 families

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7 January 2021

Two different XY-quadrivalent associations and impairment of fertility in men.

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7 January 2021

Meiotic chromosome segregation in human t(11;22)(q23;q11) carriers: a theoretical consideration

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7 January 2021

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Regions of genomic instability on 22q11 and 11q23 as the etiology for the recurrent constitutional t(11;22).

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Not all chromosome imbalance resulting from the 11q;22q translocation is due to 3:1 segregation in first meiosis

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Dual color fluorescence in situ hybridization to investigate aneuploidy in sperm from 33 normal males and a man with a t(2;4;8)(q23;q27;p21)

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7 January 2021

Pachytene analysis of a man with a 13q;14q translocation and infertility. Behavior of the trivalent and nonrandom association with the sex vesicle

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7 January 2021

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7 January 2021

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7 January 2021

Molecular analysis of the chromosomal equipment in spermatozoa of a 46, XY, t(7;8) (q11.21;cen) carrier by using fluorescence in situ hybridization

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7 January 2021

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7 January 2021

FISH analysis of the chromosomal status of spermatozoa from three men with 45,XY,der(13;14)(q10;q10) karyotype

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7 January 2021

Meiotic segregation analysis by FISH investigation of spermatozoa of a 46,Y,der(X),t(X;Y)(qter-->p22::q11-->qter) carrier

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7 January 2021

Meiotic segregation of a t(7;8)(q11.21;cen) translocation in two carrier brothers

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7 January 2021

Outcome of preimplantation genetic diagnosis of translocations

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7 January 2021

Chromosome abnormalities found among 34,910 newborn children: results from a 13-year incidence study in Arhus, Denmark

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7 January 2021

Meiotic segregation analysis in a t(4;8) carrier: comparison of FISH methods on sperm chromosome metaphases and interphase sperm nuclei.

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7 January 2021

Aneuploid and unbalanced sperm in two translocation carriers: evaluation of the genetic risk

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7 January 2021

Unusual segregation of t(11;22) resulting from crossing-over followed by 3:1 disjunction at meiosis I

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7 January 2021

Fluorescence in situ hybridisation (FISH) analysis of chromosome segregation and interchromosomal effect in spermatozoa of a reciprocal translocation t(9,10)(q11;p11.1) carrier

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7 January 2021

Sperm nuclei analysis of a Robertsonian t(14q21q) carrier, by FISH, using three plasmids and two YAC probes

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7 January 2021

Meiotic segregation in males heterozygote for reciprocal translocations: analysis of sperm nuclei by two and three colour fluorescence in situ hybridization

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7 January 2021

A direct demonstration of somatically paired heterochromatin of human chromosomes

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Clustered 11q23 and 22q11 breakpoints and 3:1 meiotic malsegregation in multiple unrelated t(11;22) families

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7 January 2021

Aneuploidy in human spermatozoa: FISH analysis in men with constitutional chromosomal abnormalities, and in infertile men.

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7 January 2021

The unbalanced offspring of the male carriers of the 11q;22q translocation: nondisjunction at meiosis II in a balanced spermatocyte.

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7 January 2021

Numerical chromosome abnormalities in the spermatozoa of the fathers of children with trisomy 21 of paternal origin: generalised tendency to meiotic non-disjunction

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7 January 2021

Unusual segregation for 11q;22q parental translocation in a triplet pregnancy: prenatal diagnosis in chorionic villi and amniotic fluid

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7 January 2021

Human male recombination maps for individual chromosomes

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Trisomy 21 Down syndrome. II. Structural chromosome rearrangements in the parents.

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Preimplantation genetic diagnosis and sperm analysis by fluorescence in-situ hybridization for the most common reciprocal translocation t(11;22).

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7 January 2021

Meiotic Segregation, Recombination, and Gamete Aneuploidy Assessed in a t(1;10)(p22.1;q22.3) Reciprocal Translocation Carrier by Three- and Four-Probe Multicolor FISH in Sperm

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7 January 2021

Meiotic and synaptonemal complex studies in a 14/21 translocation carrier

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7 January 2021

Sephadex filtration and human serum albumin gradients do not select spermatozoa by sex chromosome: a fluorescent in-situ hybridization study

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7 January 2021

A study of reciprocal translocations and inversions detected by light microscopy with special reference to origin, segregation, and recurrent abnormalities

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7 January 2021

10.1016/S1472-6483(10)61774-9

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7 January 2020

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