Cytogenetic analysis of meiotic segregation in sperm from two males heterozygous for reciprocal translocations using PRINS and humster techniques.

No abstract is available for this paper.

• Publication year

  1997

• Venue

  Cytogenetics and Cell Genetics

• Publication date

  Unknown publication date

• Fields of study

  Biology, Medicine

• Identifiers
  DOI 10.1159/000134657PMID 9465888
• External record

  Open on Semantic Scholar

• Source metadata

  Semantic Scholar, PubMed

• No claims are published for this paper.

• No concepts are published for this paper.

• Meiotic analysis by FISH of a human male 46,XY,t(15;20)(q11.2;q11.2) translocation heterozygote: quadrivalent configuration, orientation and first meiotic segregation

  2004cited by this paper
• Frequency and distribution of aneuploidy in human female gametes

  2004cited by this paper
• Direct detection of disomy in human sperm by the PRINS technique

  2004cited by this paper
• Meiotic and sperm chromosome studies in a reciprocal translocation t(1;2)(q32;q36)

  2004cited by this paper
• Chromosome complements in 695 sperm from three men heterozygous for reciprocal translocations, and a review of the literature.

  2004cited by this paper
• The Meiotic Segregation Pattern of a Reciprocal Translocation t(10;12)(q26.1; p13.3) by Fluorescence in situ Hybridization Sperm Analysis

  1997cited by this paper
• Assessment of aneuploidy for chromosomes 8, 9, 13, 16, and 21 in human sperm by using primed in situ labeling technique.

  1996cited by this paper
• Simultaneous detection of structural and numerical chromosome abnormalities in sperm of healthy men by multicolor fluorescence in situ hybridization

  1996cited by this paper
• Sperm chromosome complements in a man heterozygous for a reciprocal translocation 46,XY,t(9;13)(q21.1;q21.2) and a review of the literature

  1995cited by this paper
• Selection of chromosome-specific primers and their use in simple and double PRINS techniques for rapid in situ identification of human chromosomes.

  1995cited by this paper
• Segregation analysis of four translocations, t(2;18), t(3;15), t(5;7), and t(10;12), by sperm chromosome studies and a review of the literature.

  1995cited by this paper
• Meiotic segregation in males heterozygote for reciprocal translocations: analysis of sperm nuclei by two and three colour fluorescence in situ hybridization.

  1995cited by this paper
• A polymorphic alpha satellite sequence specific for human chromosome 13 detected by oligonucleotide primed in situ labelling (PRINS)

  1994cited by this paper
• Sperm chromosome complements in a man heterozygous for a reciprocal translocation t(2;3)(q24;p26).

  1994cited by this paper
• Detection of aneuploidy in human sperm by fluorescence in situ hybridization (FISH): different frequencies in fresh and stored sperm nuclei.

  1994cited by this paper
• Analysis of segregation in a human male reciprocal translocation carrier, t(1;11) (p36.3;q13.1) by two‐colour fluorescence in situ hybridization

  1994cited by this paper
• Detection of aneuploidy in human interphase spermatozoa by fluorescence in situ hybridization (FISH).

  1993cited by this paper
• Non-disjunction in human sperm: results of fluorescence in situ hybridization studies using two and three probes.

  1993cited by this paper
• Human reciprocal translocations: is the unbalanced mode at birth predictable?

  1993cited by this paper
• Sperm chromosome complements from two human reciprocal translocation heterozygotes

  1992cited by this paper
• Sperm chromosome analysis of two men heterozygous for reciprocal translocations: t(1;9)(q22;q31) and t(16;19)(q11.1;q13.3).

  1992cited by this paper
• The segregation of a translocation t(1;4) in two male carriers heterozygous for the translocation

  1992cited by this paper
• Sperm chromosome analysis of two males heterozygous for a t(2;17)(q35;p13) and t(3;8)(p13;p21) reciprocal translocation

  1992cited by this paper
• An improved method for chromosome-specific labeling of alpha satellite DNA in situ by using denatured double-stranded DNA probes as primers in a primed in situ labeling (PRINS) procedure.

  1991cited by this paper
• Sperm chromosome analysis in a man heterozygous for a reciprocal translocation 46,XY t(12;20)(q24.3;q11).

  1990cited by this paper
• Cytogenetic analysis of 400 sperm from three translocation heterozygotes

  1990cited by this paper
• Determination of Y chromosome aneuploidy in human sperm nuclei by nonradioactive in situ hybridization.

  1990cited by this paper
• Direct segregation analysis of reciprocal translocations: a study of 283 sperm karyotypes from four carriers.

  1989cited by this paper
• Meiotic segregation of human sperm chromosomes in translocation heterozygotes: report of a t(9;10)(q34;q11) and a review of the literature.

  1988cited by this paper
• Human sperm chromosome studies in a reciprocal translocation t(2;5)

  1988cited by this paper
• Cytogenetics of human sperm: meiotic segregation in two translocation carriers.

  1986cited by this paper
• Analysis of meiotic segregation in a man heterozygous for two reciprocal translocations using the hamster in vitro penetration system.

  1986cited by this paper
• A computer model for the study of segregation in reciprocal translocation carriers: application to 20 new cases.

  1986cited by this paper
• A collaborative study of the segregation of inherited chromosome structural rearrangements in 1356 prenatal diagnoses

  1984cited by this paper
• Analysis of human sperm chromosome complements from a male heterozygous for a reciprocal translocation t(11;22)(q23;q11)

  1984cited by this paper
• Chromosome segregation into the spermatozoa of two men heterozygous for different reciprocal translocations

  1983cited by this paper
• Reciprocal translocations: A way to predict the mode of imbalanced segregation by pachytene-diagram drawing

  1980cited by this paper
• Structural differences in reciprocal translocations

  1979cited by this paper
• Epidemiology of chromosome abnormalities in man.

  1977cited by this paper

• Clinical Features of Infertile Men Carrying a Chromosome 9 Translocation

  2019cites this paper
• Portadores de reorganizaciones cromosómicas: segregación meiótica en espermatogénesis y consecuencias

  2016cites this paper
• Inheritance of a translocation between chromosomes 12 and 16 in a family with recurrent miscarriages and a newborn with Down syndrome carrying the same translocation.

  2008cites this paper
• Differing mechanisms of meiotic segregation in spermatozoa from three carriers of a pericentric inversion of chromosome 8.

  2008cites this paper
• PRINS and In Situ PCR Protocols

  2006cites this paper
• Multicolor PRINS and multicolor PNA

  2006cites this paper
• Meiotic segregation analysis of reciprocal translocations both in sperms and blastomeres

  2006cites this paper
• In situ aneuploidy assessment in human sperm: the use of primed in situ and peptide nucleic acid-fluorescence in situ hybridization techniques.

  2006cites this paper
• Development and Adaptation of the PRINS Technology

  2006cites this paper
• Segregation of chromosomes in sperm of reciprocal translocation carriers: a review

  2005influential citation
• Meiotic segregation of translocations during male gametogenesis.

  2004cites this paper
• Estimation of the proportion of genetically unbalanced spermatozoa in the semen of boars carrying chromosomal rearrangements using FISH on sperm nuclei

  2004influential citation
• [From the conception of the PRINS to its coronation].

  2004cites this paper
• De la conception du PRINS

  2004cites this paper
• De la conception du PRINS à son couronnement

  2004cites this paper
• Molecular cytogenetic detection of meiotic segregation patterns in sperm nuclei of carriers of 46,XY,t(15;17)(q21; q25).

  2002cites this paper
• Sperm segregation patterns by fluorescence in situ hybridization studies of a 46,XY,t(2;6) heterozygote giving rise to a rare triploid product of conception with a 69,XXY,t(2;6)(p12;q24)der(6)t(2;6)(p12;q24)pat karyotype

  2002cites this paper
• Aneuploidy in human spermatozoa: FISH analysis in men with constitutional chromosomal abnormalities, and in infertile men.

  2001cites this paper
• FISH analysis of the chromosomal status of spermatozoa from three men with 45,XY,der(13;14)(q10;q10) karyotype.

  2001cites this paper
• Detecció i incidència d'anomalies cromosòmiques en espermatozoides humans

  2001influential citation
• Study of the occurrence of interchromosomal effect in spermatozoa of chromosomal rearrangement carriers by fluorescence in-situ hybridization and primed in-situ labelling techniques.

  2001cites this paper
• Cooperation of selection and meiotic mechanisms in the production of imbalances in reciprocal translocations

  2000cites this paper
• Interchromosomal effects for chromosome 21 in carriers of structural chromosome reorganizations determined by fluorescence in situ hybridization on sperm nuclei

  2000cites this paper
• 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

  1999cites this paper
• Sperm analysis in a subfertile male with a Y;16 translocation, using four-color FISH

  1999influential citation
• 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)

  1999cites this paper
• One normal child and a chromosomally balanced/normal twin after intracytoplasmic sperm injection in a male with a de-novo t(Y;16) translocation.

  1998cites this paper
• Chiasma distributions and chromosome segregation in male and female translocation heterozygous mice analysed using FISH

  1998cites this paper
• Sperm segregation analysis of a complex chromosome rearrangement, 2;22;11, by whole chromosome painting

  1998cites this paper