(Q35194779)

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Evidence for human meiotic recombination interference obtained through construction of a short tandem repeat-polymorphism linkage map of chromosome 19.

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scholarly article

1 reference

Europe PubMed Central

PubMed publication ID

7 August 2017

Evidence for human meiotic recombination interference obtained through construction of a short tandem repeat-polymorphism linkage map of chromosome 19. (English)

1 reference

Europe PubMed Central

PubMed publication ID

7 August 2017

short tandem repeat

1 reference

based on heuristic

inferred from title

Bronya J. B. Keats

8

object named as

B Keats

1 reference

Europe PubMed Central

PubMed publication ID

7 August 2017

author name string

J L Weber

1

1 reference

Europe PubMed Central

PubMed publication ID

7 August 2017

Z Wang

2

1 reference

Europe PubMed Central

PubMed publication ID

7 August 2017

K Hansen

3

1 reference

Europe PubMed Central

PubMed publication ID

7 August 2017

M Stephenson

4

1 reference

Europe PubMed Central

PubMed publication ID

7 August 2017

C Kappel

5

1 reference

Europe PubMed Central

PubMed publication ID

7 August 2017

S Salzman

6

1 reference

Europe PubMed Central

PubMed publication ID

7 August 2017

P J Wilkie

7

1 reference

Europe PubMed Central

PubMed publication ID

7 August 2017

N C Dracopoli

9

1 reference

Europe PubMed Central

PubMed publication ID

7 August 2017

B F Brandriff

10

1 reference

Europe PubMed Central

PubMed publication ID

7 August 2017

language of work or name

0 references

publication date

1 November 1993

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Europe PubMed Central

PubMed publication ID

7 August 2017

American Journal of Human Genetics

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Europe PubMed Central

PubMed publication ID

7 August 2017

53

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Europe PubMed Central

PubMed publication ID

7 August 2017

5

1 reference

Europe PubMed Central

PubMed publication ID

7 August 2017

1079-1095

1 reference

Europe PubMed Central

PubMed publication ID

7 August 2017

Incidence and origin of "null" alleles in the (AC)n microsatellite markers.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1682307

13 July 2018

A microsatellite genetic linkage map of human chromosome 13.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1682307

13 July 2018

Fluorescence in situ hybridization mapping of human chromosome 19: cytogenetic band location of 540 cosmids and 70 genes or DNA markers

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1682307

13 July 2018

Chiasma distribution at diakinesis in the normal human male

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1682307

13 July 2018

Multilocus linkage analysis in humans: detection of linkage and estimation of recombination

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1682307

13 July 2018

A linkage map of mouse chromosome 12: localization of Igh and effects of sex and interference on recombination.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1682307

13 July 2018

Orangutan fetal globin genes. Nucleotide sequence reveal multiple gene conversions during hominid phylogeny

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1682307

13 July 2018

Abundant class of human DNA polymorphisms which can be typed using the polymerase chain reaction

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1682307

13 July 2018

Chiasma-based models of multilocus recombination: increased power for exclusion mapping and gene ordering.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1682307

13 July 2018

A high-resolution, fluorescence-based, semiautomated method for DNA fingerprinting

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1682307

13 July 2018

Dinucleotide repeat polymorphism at the D19S75 locus

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1682307

13 July 2018

Chiasma-based genetic maps of chromosome 21.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1682307

13 July 2018

Development and applications of a molecular genetic linkage map of the mouse genome

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1682307

13 July 2018

Dinucleotide repeat polymorphism in CEA gene

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1682307

13 July 2018

cDNA and genomic cloning of HRC, a human sarcoplasmic reticulum protein, and localization of the gene to human chromosome 19 and mouse chromosome 7

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1682307

13 July 2018

Dinucleotide repeat polymorphism at the D19S49 locus

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1682307

13 July 2018

Influence of aberrant observations on high-resolution linkage analysis outcomes

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1682307

13 July 2018

Dinucleotide repeat polymorphism at the RYR1 locus (19q13.1).

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1682307

13 July 2018

Gene conversions within the skeletal myosin multigene family

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1682307

13 July 2018

Human glandular kallikrein genes: Genetic and physical mapping of the KLK1 locus using a highly polymorphic microsatellite PCR marker

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1682307

13 July 2018

Isolation and chromosomal assignment of 100 highly informative human simple sequence repeat polymorphisms

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1682307

13 July 2018

Assembly and analysis of cosmid contigs in the CEA-gene family region of human chromosome 19

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1682307

13 July 2018

Robustness of the no-interference model for ordering genetic markers

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1682307

13 July 2018

Dinucleotide repeat polymorphism at the D19S191 locus

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1682307

13 July 2018

Myotonic dystrophy mutation: an unstable CTG repeat in the 3' untranslated region of the gene

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1682307

13 July 2018

Microsatellites for linkage analysis of genetic traits

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1682307

13 July 2018

A second-generation linkage map of the human genome

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1682307

13 July 2018

High-resolution physical mapping of four microsatellite repeat markers near the RYR1 locus on chromosome 19q13.1 and apparent exclusion of the MHS locus from this region in two malignant hyperthermia susceptible families

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1682307

13 July 2018

Systematic detection of errors in genetic linkage data

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1682307

13 July 2018

Chromlook: an interactive program for error detection and mapping in reference linkage data

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1682307

13 July 2018

Human chromosome 8 linkage map based on short tandem repeat polymorphisms: effect of genotyping errors

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1682307

13 July 2018

Two hypervariable minisatellites D19S192 (pMS207.2) and D19S193 (pMS301.2) located at the distal ends of 19p and 19q respectively

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1682307

13 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=1682307

13 July 2018

Fluorescence in situ hybridization mapping of human chromosome 19: mapping and verification of cosmid contigs formed by random restriction enzyme fingerprinting

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1682307

13 July 2018

La carte des microsatellites est arrivée! [The map of microsatellites has arrived!].

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1682307

13 July 2018

Linkage disequilibrium mapping in isolated founder populations: diastrophic dysplasia in Finland

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1682307

28 July 2018

A primary map of ten DNA markers and two serological markers for human chromosome 19

1 reference

https://pubmed.ncbi.nlm.nih.gov/8213834

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A molecular genetic linkage map of mouse chromosome 4 including the localization of several proto-oncogenes

1 reference

https://pubmed.ncbi.nlm.nih.gov/8213834

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Mapping of human chromosome 5 microsatellite DNA polymorphisms

1 reference

https://pubmed.ncbi.nlm.nih.gov/8213834

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Estimation of microsatellite mutation rates in recombinant inbred strains of mouse

1 reference

https://pubmed.ncbi.nlm.nih.gov/8213834

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Abnormal segregation of alleles in CEPH pedigree DNAs arising from allele loss in lymphoblastoid DNA

1 reference

https://pubmed.ncbi.nlm.nih.gov/8213834

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Dinucleotide repeat polymorphism at the hormone sensitive lipase (LIPE) locus

1 reference

https://pubmed.ncbi.nlm.nih.gov/8213834

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Unstable DNA may be responsible for the incomplete penetrance of the myotonic dystrophy phenotype

1 reference

https://pubmed.ncbi.nlm.nih.gov/8213834

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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PMC publication ID

1 reference

Europe PubMed Central

PubMed publication ID

7 August 2017

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

7 August 2017

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