(Q34385650)

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Genetic analysis of meiotic recombination in humans by use of sperm typing: reduced recombination within a heterozygous paracentric inversion of chromosome 9q32-q34.3.

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Europe PubMed Central

PubMed publication ID

1 August 2017

Genetic analysis of meiotic recombination in humans by use of sperm typing: reduced recombination within a heterozygous paracentric inversion of chromosome 9q32-q34.3. (English)

1 reference

Europe PubMed Central

PubMed publication ID

1 August 2017

1 reference

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author name string

G M Brown

1

1 reference

Europe PubMed Central

PubMed publication ID

1 August 2017

M Leversha

2

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Europe PubMed Central

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1 August 2017

M Hulten

3

1 reference

Europe PubMed Central

PubMed publication ID

1 August 2017

M A Ferguson-Smith

4

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Europe PubMed Central

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1 August 2017

N A Affara

5

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1 August 2017

R A Furlong

6

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1 August 2017

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publication date

1 June 1998

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Europe PubMed Central

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1 August 2017

American Journal of Human Genetics

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Europe PubMed Central

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1 August 2017

62

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Europe PubMed Central

PubMed publication ID

1 August 2017

6

1 reference

Europe PubMed Central

PubMed publication ID

1 August 2017

1484-1492

1 reference

Europe PubMed Central

PubMed publication ID

1 August 2017

Sequential G-banding FISH on human sperm chromosomes

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1377142

6 July 2018

Report on the Fifth International Workshop on Chromosome 9 held at Eynsham, Oxfordshire, UK, September 4-6, 1996.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1377142

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Recombination patterns around the breakpoints of a balanced 1;11 autosomal translocation associated with major mental illness.

1 reference

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6 July 2018

Individual variation in recombination among human males

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1377142

6 July 2018

Analysis of meiotic segregation, using single-sperm typing: meiotic drive at the myotonic dystrophy locus.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1377142

6 July 2018

Paracentric inversions: a review

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1377142

6 July 2018

Analysis of four microsatellite markers on the long arm of chromosome 9 by meiotic recombination in flow-sorted single sperm.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1377142

6 July 2018

Physical mapping within the tuberous sclerosis linkage group in region 9q32-q34.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1377142

6 July 2018

Multipoint mapping calculations for sperm-typing data.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1377142

6 July 2018

Multipoint linkage map of the human pseudoautosomal region, based on single-sperm typing: do double crossovers occur during male meiosis?

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1377142

6 July 2018

Physical analysis of the tuberous sclerosis region in 9q34.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1377142

6 July 2018

Further studies on bivalent chiasma frequency in human males with normal karyotypes.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1377142

6 July 2018

Construction of multilocus genetic linkage maps in humans

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1377142

6 July 2018

Amplification and analysis of DNA sequences in single human sperm and diploid cells

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1377142

6 July 2018

Single-sperm typing: determination of genetic distance between the G gamma-globin and parathyroid hormone loci by using the polymerase chain reaction and allele-specific oligomers

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1377142

6 July 2018

The meiotic behavior of an inversion in Caenorhabditis elegans

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1377142

6 July 2018

Whole genome amplification from a single cell: implications for genetic analysis

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1377142

6 July 2018

Construction of a GT polymorphism map of human 9q

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1377142

6 July 2018

Meiotic analysis of a pericentric inversion, inv(7) (p22q32), in the father of a child with a duplication-deletion of chromosome 7

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1377142

6 July 2018

[Mutagenesis and interchromosomal effect on crossing over in Drosophila]

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1377142

27 October 2018

CAG repeat length variation in sperm from a patient with Kennedy's disease

1 reference

https://pubmed.ncbi.nlm.nih.gov/9585591

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Genetic mapping of F13A to BTA23 by sperm typing: difference in recombination rate between bulls in the DYA-PRL interval

1 reference

https://pubmed.ncbi.nlm.nih.gov/9585591

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A 37-marker PCR-based genetic linkage map of human chromosome 9: observations on mutations and positive interference

1 reference

https://pubmed.ncbi.nlm.nih.gov/9585591

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Single sperm analysis of the CAG repeats in the gene for Machado-Joseph disease (MJD1): evidence for non-Mendelian transmission of the MJD1 gene and for the effect of the intragenic CGG/GGG polymorphism on the intergenerational instability

1 reference

https://pubmed.ncbi.nlm.nih.gov/9585591

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Chiasma frequency and distribution in a sample of human males: chromosomes 1, 2, and 9

1 reference

https://pubmed.ncbi.nlm.nih.gov/9585591

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Studies on chiasma frequency and distribution in two fertile men carrying reciprocal translocations; one with a t(9;10) karyotype and one with a t(Y;10) karyotype

1 reference

https://pubmed.ncbi.nlm.nih.gov/9585591

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Sperm chromosome analysis in a man heterozygous for a paracentric inversion of chromosome 7 (q11q22)

1 reference

https://pubmed.ncbi.nlm.nih.gov/9585591

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Electron microscopic investigations of synaptonemal complexes in an infertile human male carrier of a pericentric inversion inv(1)(p32q42). Regular loop formation but defective synapsis including a possible interchromosomal effect

1 reference

https://pubmed.ncbi.nlm.nih.gov/9585591

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

EM investigations of surface spread synaptonemal complexes in a human male carrier of a pericentric inversion inv(13)(p12q14): the role of heterosynapsis for spermatocyte survival

1 reference

https://pubmed.ncbi.nlm.nih.gov/9585591

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Programs for pedigree analysis: Mendel, Fisher, and dGene

1 reference

https://pubmed.ncbi.nlm.nih.gov/9585591

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Analysis of chiasma frequency and first meiotic segregation in a human male reciprocal translocation heterozygote, t(1;11)(p36.3;q13.1), using fluorescence in situ hybridisation

1 reference

https://pubmed.ncbi.nlm.nih.gov/9585591

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

CEPH Consortium Map of Chromosome 9

1 reference

https://pubmed.ncbi.nlm.nih.gov/9585591

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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1 reference

Europe PubMed Central

PubMed publication ID

1 August 2017

PMC publication ID

1 reference

Europe PubMed Central

PubMed publication ID

1 August 2017

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

1 August 2017

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