(Q28208062)

2

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R J Gardner

5

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M P Short

6

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E S Roach

8

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Kandt RS

1

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11 September 2022

Haines JL

2

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11 September 2022

Smith M

3

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11 September 2022

Northrup H

4

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11 September 2022

Gardner RJ

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11 September 2022

Short MP

6

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11 September 2022

Dumars K

7

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11 September 2022

Roach ES

8

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11 September 2022

Steingold S

9

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11 September 2022

Wall S

10

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Causes of Death in Patients With Tuberous Sclerosis

11 September 2022

language of work or name

English

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publication date

September 1992

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published in

Nature Genetics

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volume

2

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issue

1

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page(s)

37-41

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cites work

1 reference

Expansion of an unstable DNA region and phenotypic variation in myotonic dystrophy

21 January 2018

1 reference

Cloning of the essential myotonic dystrophy region and mapping of the putative defect

21 January 2018

1 reference

Androgen receptor gene mutations in X-linked spinal and bulbar muscular atrophy

21 January 2018

1 reference

Rapid genetic analysis of families with polycystic kidney disease 1 by means of a microsatellite marker

21 January 2018

1 reference

Incidence and prevalence of tuberous sclerosis in Rochester, Minnesota, 1950 through 1982

21 January 2018

1 reference

7 January 2021

EVIDENCE THAT THE GENE FOR TUBEROUS SCLEROSIS IS ON CHROMOSOME 9

1 reference

7 January 2021

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

1 reference

7 January 2021

Linkage of tuberous sclerosis to ABO blood group

1 reference

7 January 2021

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

1 reference

7 January 2021

Genetic recombination between tuberous sclerosis and oncogene v-abl

1 reference

7 January 2021

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

1 reference

7 January 2021

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

1 reference

7 January 2021

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

1 reference

7 January 2021

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

1 reference

7 January 2021

Linkage studies in tuberous sclerosis. Chromosome 9?, 11?, or maybe 14!

1 reference

7 January 2021

Evidence for genetic heterogeneity in tuberous sclerosis

1 reference

7 January 2021

Genetic heterogeneity in tuberous sclerosis

1 reference

7 January 2021

REPORT on the First International Workshop on Chromosome 9 held at Girton College Cambridge, UK, 22?24 March, 1992

1 reference

7 January 2021

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

1 reference

7 January 2021

The cystic renal lesion in tuberous sclerosis

1 reference

7 January 2021

Heritable unstable DNA sequences

1 reference

7 January 2021

Detection of an unstable fragment of DNA specific to individuals with myotonic dystrophy

1 reference

7 January 2021

Instability of a 550-base pair DNA segment and abnormal methylation in fragile X syndrome

1 reference

7 January 2021

The gene for autosomal dominant polycystic kidney disease lies in a 750-kb CpG-rich region

1 reference

7 January 2021

Construction of a GT polymorphism map of human 9q

1 reference

7 January 2021

Dinucleotide repeat polymorphism at the D11S35 locus

1 reference

7 January 2021

PCR detection of the Mspl (Aa) RFLP at the human phenylalanine hydroxylase (PAH) locus

1 reference

7 January 2021

Report of the Committee on Methods of Linkage Analysis and Reporting

1 reference

7 January 2021

Identifiers

DOI

10.1038/NG0992-37

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