(Q34044235)

30 July 2017

0 references

A duplication in chromosome 4q35 is associated with hereditary benign intraepithelial dyskeratosis. (English)

1 reference

30 July 2017

12

1 reference

30 July 2017

R R Allingham

1

1 reference

30 July 2017

B Seo

2

1 reference

30 July 2017

E Rampersaud

3

1 reference

30 July 2017

M Bembe

4

1 reference

30 July 2017

P Challa

5

1 reference

30 July 2017

N Liu

6

1 reference

30 July 2017

T Parrish

7

1 reference

30 July 2017

L Karolak

8

1 reference

30 July 2017

J Gilbert

9

1 reference

30 July 2017

M A Pericak-Vance

10

1 reference

30 July 2017

G K Klintworth

11

1 reference

30 July 2017

language of work or name

English

0 references

publication date

16 January 2001

1 reference

American Journal of Human Genetics

30 July 2017

published in

1 reference

30 July 2017

volume

68

1 reference

30 July 2017

issue

2

1 reference

30 July 2017

page(s)

491-494

1 reference

Identification of a new locus for autosomal recessive Charcot-Marie-Tooth disease with focally folded myelin on chromosome 11p15.

30 July 2017

cites work

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1235282

The VITESSE algorithm for rapid exact multilocus linkage analysis via genotype set-recoding and fuzzy inheritance

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1235282

Hereditary benign intraepithelial dyskeratosis

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1235282

The fat tumor suppressor gene in Drosophila encodes a novel member of the cadherin gene superfamily

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1235282

Dinucleotide repeat polymorphism at the D17S518 locus

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1235282

Detection of DNA sequence polymorphisms in human genomic DNA by using denaturing gradient gel blots

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1235282

Hereditary Dyskeratosis of the Perilimbal Conjunctiva.

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1235282

Molecular cloning and tissue expression of FAT, the human homologue of the Drosophila fat gene that is located on chromosome 4q34-q35 and encodes a putative adhesion molecule

28 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1235282

Hereditary benign intraepithelial dyskeratosis. A report of two cases from Texas.

28 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1235282

The peripheral myelin protein gene PMP-22 is contained within the Charcot-Marie-Tooth disease type 1A duplication

28 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1235282

Hereditary benign intraepithelial dyskeratosis. II. Oral manifestations and hereditary transmission

28 October 2018

1 reference

12 December 2020

Hereditary benign intraepithelial dyskeratosis

1 reference

12 December 2020

Corneal Manifestations of Hereditary Benign Intraepithelial Dyskeratosis

1 reference

12 December 2020

Duplication in chromosome 17p11.2 in Charcot-Marie-Tooth neuropathy type 1a (CMT 1a)

1 reference

12 December 2020

Identifiers

DOI

10.1086/318194

1 reference

30 July 2017

1 reference

30 July 2017

1 reference