Genetic heterogeneity in LEOPARD syndrome: two families with no mutations in PTPN11. (Q45250214)

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scientific article published on 10 December 2004

Language	Label	Description	Also known as
English	Genetic heterogeneity in LEOPARD syndrome: two families with no mutations in PTPN11.	scientific article published on 10 December 2004

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scholarly article

1 reference

Europe PubMed Central

PubMed publication ID

11 December 2017

Genetic heterogeneity in LEOPARD syndrome: two families with no mutations in PTPN11. (English)

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Europe PubMed Central

PubMed publication ID

11 December 2017

LEOPARD syndrome

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inferred from title

Ruth Newbury-Ecob

4

object named as

Ruth Newbury-Ecob

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Europe PubMed Central

PubMed publication ID

11 December 2017

author name string

Kamini Kalidas

1

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Europe PubMed Central

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11 December 2017

Adam C Shaw

2

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Europe PubMed Central

PubMed publication ID

11 December 2017

Andrew H Crosby

3

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Europe PubMed Central

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11 December 2017

Lynn Greenhalgh

5

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Europe PubMed Central

PubMed publication ID

11 December 2017

Isabel K Temple

6

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Europe PubMed Central

PubMed publication ID

11 December 2017

Caroline Law

7

1 reference

Europe PubMed Central

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11 December 2017

Amisha Patel

8

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11 December 2017

Michael A Patton

9

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11 December 2017

Steve Jeffery

10

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11 December 2017

publication date

10 December 2004

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11 December 2017

Journal of Human Genetics

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11 December 2017

50

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11 December 2017

1

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11 December 2017

21-25

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11 December 2017

Strategies for multilocus linkage analysis in humans

1 reference

https://pubmed.ncbi.nlm.nih.gov/15690106

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Multiple lentigines syndrome. Case report and review of the literature

1 reference

https://pubmed.ncbi.nlm.nih.gov/15690106

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Exclusion of candidate genes and loci for multiple lentigines syndrome

1 reference

https://pubmed.ncbi.nlm.nih.gov/15690106

12 December 2020

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inferred from PubMed ID database lookup

Clinical and molecular analysis of 30 patients with multiple lentigines LEOPARD syndrome.

1 reference

https://pubmed.ncbi.nlm.nih.gov/15690106

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Grouping of multiple-lentigines/LEOPARD and Noonan syndromes on the PTPN11 gene

1 reference

https://pubmed.ncbi.nlm.nih.gov/15690106

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Mutations in PTPN11, encoding the protein tyrosine phosphatase SHP-2, cause Noonan syndrome

1 reference

https://pubmed.ncbi.nlm.nih.gov/15690106

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

PTPN11 mutations in Noonan syndrome: molecular spectrum, genotype-phenotype correlation, and phenotypic heterogeneity

1 reference

https://pubmed.ncbi.nlm.nih.gov/15690106

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Multiple lentigines syndrome (LEOPARD syndrome or progressive cardiomyopathic lentiginosis)

1 reference

https://pubmed.ncbi.nlm.nih.gov/15690106

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Mapping a gene for Noonan syndrome to the long arm of chromosome 12

1 reference

https://pubmed.ncbi.nlm.nih.gov/15690106

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Unifying link between Noonan's and Leopard syndromes?

1 reference

https://pubmed.ncbi.nlm.nih.gov/15690106

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

PTPN11 mutations in LEOPARD syndrome

1 reference

https://pubmed.ncbi.nlm.nih.gov/15690106

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Multiple Lentigenes Syndrome

1 reference

https://pubmed.ncbi.nlm.nih.gov/15690106

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A novel PTPN11 mutation in LEOPARD syndrome.

1 reference

https://pubmed.ncbi.nlm.nih.gov/15690106

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1007/S10038-004-0212-X

1 reference

Europe PubMed Central

PubMed publication ID

11 December 2017

Dimensions Publication ID

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PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

11 December 2017

ResearchGate publication ID

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