(Q43169975)

15 November 2017

0 references

STK11 status and intussusception risk in Peutz-Jeghers syndrome (English)

1 reference

15 November 2017

23

1 reference

15 November 2017

N Hearle

1

1 reference

15 November 2017

V Schumacher

2

1 reference

15 November 2017

F H Menko

3

1 reference

15 November 2017

S Olschwang

4

1 reference

15 November 2017

L A Boardman

5

1 reference

15 November 2017

J J P Gille

6

1 reference

15 November 2017

J J Keller

7

1 reference

15 November 2017

A M Westerman

8

1 reference

15 November 2017

R J Scott

9

1 reference

15 November 2017

W Lim

10

1 reference

15 November 2017

J D Trimbath

11

1 reference

15 November 2017

F M Giardiello

12

1 reference

15 November 2017

S B Gruber

13

1 reference

15 November 2017

G J A Offerhaus

14

1 reference

15 November 2017

F W M D E Rooij

15

1 reference

15 November 2017

J H P Wilson

16

1 reference

15 November 2017

A Hansmann

17

1 reference

15 November 2017

G Möslein

18

1 reference

15 November 2017

B Royer-Pokora

19

1 reference

15 November 2017

T Vogel

20

1 reference

15 November 2017

R K S Phillips

21

1 reference

15 November 2017

A D Spigelman

22

1 reference

15 November 2017

language of work or name

English

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publication date

1 August 2006

1 reference

Journal of Medical Genetics

15 November 2017

1 reference

15 November 2017

43

1 reference

15 November 2017

8

1 reference

15 November 2017

e41

1 reference

Exonic STK11 deletions are not a rare cause of Peutz-Jeghers syndrome

15 November 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2564597

High proportion of large genomic STK11 deletions in Peutz-Jeghers syndrome

25 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2564597

Online Mendelian Inheritance in Man (OMIM), a knowledgebase of human genes and genetic disorders

25 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2564597

Genotype-phenotype correlations in Peutz-Jeghers syndrome

25 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2564597

Mutation analysis of the STK11/LKB1 gene and clinical characteristics of an Australian series of Peutz-Jeghers syndrome patients

25 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2564597

Genetic heterogeneity in Peutz-Jeghers syndrome

25 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2564597

STK11/LKB1 germline mutations are not identified in most Peutz-Jeghers syndrome patients

25 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2564597

Novel mutations in the LKB1/STK11 gene in Dutch Peutz-Jeghers families

25 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2564597

Germline mutations of the LKB1 (STK11) gene in Peutz-Jeghers patients

25 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2564597

Mutations and impaired function of LKB1 in familial and non-familial Peutz-Jeghers syndrome and a sporadic testicular cancer.

25 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2564597

Nine novel germline mutations of STK11 in ten families with Peutz-Jeghers syndrome

25 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2564597

25 May 2018

Peutz-Jeghers syndrome

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2564597

A serine/threonine kinase gene defective in Peutz-Jeghers syndrome

25 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2564597

Peutz-Jeghers syndrome is caused by mutations in a novel serine threonine kinase

25 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2564597

Peutz-Jeghers syndrome: confirmation of linkage to chromosome 19p13.3 and identification of a potential second locus, on 19q13.4.

25 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2564597

STK11 genotyping and cancer risk in Peutz-Jeghers syndrome

25 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2564597

Rapid detection of DNA sequence variants by conformation-sensitive capillary electrophoresis.

15 August 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2564597

15 August 2018

Identifiers

DOI

10.1136/JMG.2005.040535

1 reference

release_lpfhq4dtsrdn5gravlo7spzcmu

15 November 2017

1 reference

Fatcat

https://api.fatcat.wiki/v0/release/lpfhq4dtsrdn5gravlo7spzcmu

mapped directly with Wikidata item

24 November 2022

based on heuristic

1 reference

15 November 2017

PubMed publication ID

16882735

1 reference