(Q33594756)

English

Linkage investigation of three putative tuberous sclerosis determining loci on chromosomes 9q, 11q, and 12q. The Tuberous Sclerosis Collaborative Group

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scholarly article

1 reference

Europe PubMed Central

PubMed publication ID

28 July 2017

Linkage investigation of three putative tuberous sclerosis determining loci on chromosomes 9q, 11q, and 12q. The Tuberous Sclerosis Collaborative Group (English)

1 reference

Europe PubMed Central

PubMed publication ID

28 July 2017

1 reference

based on heuristic

inferred from title

tuberous sclerosis

1 reference

based on heuristic

inferred from title

author name string

J R Sampson

1

1 reference

Europe PubMed Central

PubMed publication ID

28 July 2017

L A Janssen

2

1 reference

Europe PubMed Central

PubMed publication ID

28 July 2017

L A Sandkuijl

3

1 reference

Europe PubMed Central

PubMed publication ID

28 July 2017

language of work or name

0 references

publication date

1 December 1992

1 reference

Europe PubMed Central

PubMed publication ID

28 July 2017

Journal of Medical Genetics

1 reference

Europe PubMed Central

PubMed publication ID

28 July 2017

29

1 reference

Europe PubMed Central

PubMed publication ID

28 July 2017

12

1 reference

Europe PubMed Central

PubMed publication ID

28 July 2017

861-866

1 reference

Europe PubMed Central

PubMed publication ID

28 July 2017

Extensions to pedigree analysis. V. Optimal calculation of Mendelian likelihoods

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1016202

21 June 2018

A primary genetic linkage map for human chromosome 12.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1016202

21 June 2018

A mapped set of genetic markers for human chromosome 9.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1016202

21 June 2018

Hydrocephalus, tall stature, joint laxity, and kyphoscoliosis: a new inherited disorder of connective tissue?

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1016202

21 June 2018

Linkage of the tuberous sclerosis locus to a DNA polymorphism detected by v-abl

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1016202

21 June 2018

Evidence that the gene for tuberous sclerosis is on chromosome 9

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1016202

21 June 2018

Identification of the cystic fibrosis gene: chromosome walking and jumping

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1016202

21 June 2018

Mapping of a gene determining tuberous sclerosis to human chromosome 11q14-11q23.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1016202

21 June 2018

Genetic linkage and heterogeneity in type I Charcot-Marie-Tooth disease (hereditary motor and sensory neuropathy type I).

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1016202

21 June 2018

Further mapping of an ataxia-telangiectasia locus to the chromosome 11q23 region

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1016202

21 June 2018

A comparative study on genetic heterogeneity in tuberous sclerosis: evidence for one gene on 9q34 and a second gene on 11q22-23.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1016202

21 June 2018

Genetic heterogeneity in tuberous sclerosis

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1016202

21 June 2018

Localization of one gene for tuberous sclerosis within 9q32-9q34, and further evidence for heterogeneity

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1016202

21 June 2018

Tuberous sclerosis in a child with de novo translocation t(3; 12) (p26.3; q23.3)

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1016202

21 June 2018

Computer simulation of linkage and heterogeneity in tuberous sclerosis: a critical evaluation of the collaborative family data

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1016202

21 June 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=1016202

21 June 2018

Molecular basis of myotonic dystrophy: expansion of a trinucleotide (CTG) repeat at the 3' end of a transcript encoding a protein kinase family member.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1016202

21 June 2018

A third gene locus for tuberous sclerosis is closely linked to the phenylalanine hydroxylase gene locus

1 reference

https://pubmed.ncbi.nlm.nih.gov/1479600

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Absence of linkage of ABO blood group locus to familial tuberous sclerosis

1 reference

https://pubmed.ncbi.nlm.nih.gov/1479600

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Linkage analysis and family classification under heterogeneity

1 reference

https://pubmed.ncbi.nlm.nih.gov/1479600

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Genetic Heterogeneity of Polycystic Kidney Disease in Europe1

1 reference

https://pubmed.ncbi.nlm.nih.gov/1479600

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

An Attempt to Map Two Genes for Tuberous Sclerosis Using Novel Two-Point Methods

1 reference

https://pubmed.ncbi.nlm.nih.gov/1479600

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A detailed genetic map of the long arm of chromosome 11

1 reference

https://pubmed.ncbi.nlm.nih.gov/1479600

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Genetic Heterogeneity in Tuberous Sclerosis. Study of a Large Collaborative Dataset

1 reference

https://pubmed.ncbi.nlm.nih.gov/1479600

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1136/JMG.29.12.861

1 reference

Europe PubMed Central

PubMed publication ID

28 July 2017

PMC publication ID

1 reference

Europe PubMed Central

PubMed publication ID

28 July 2017

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

28 July 2017

ResearchGate publication ID

0 references

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