(Q79361913)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17107387%20AND%20SRC:MED&resulttype=core&format=json

21 December 2019

title

Ectodermal dysplasia of hair and nail type: mapping of a novel locus to chromosome 17p12-q21.2. (English)

1 reference

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21 December 2019

1 reference

1

1 reference

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21 December 2019

Musharraf Jelani

2

1 reference

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21 December 2019

Kwanghyuk Lee

3

1 reference

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21 December 2019

10

S M Leal

1 reference

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21 December 2019

author name string

G Ali

4

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21 December 2019

M S Chishti

5

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21 December 2019

A Wali

6

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21 December 2019

A Gul

7

1 reference

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21 December 2019

P John

8

1 reference

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21 December 2019

M J Hassan

9

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21 December 2019

W Ahmad

11

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21 December 2019

language of work or name

English

0 references

publication date

1 December 2006

1 reference

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British Journal of Dermatology

21 December 2019

published in

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21 December 2019

volume

155

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21 December 2019

issue

6

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21 December 2019

page(s)

1184-1190

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Refined mapping of Naegeli-Franceschetti- Jadassohn syndrome to a 6 cM interval on chromosome 17q11.2-q21 and investigation of candidate genes

21 December 2019

cites work

1 reference

12 December 2020

Exposing the human nude phenotype

1 reference

12 December 2020

Hair-nail dysplasia - a new pure autosomal dominant ectodermal dysplasia

1 reference

12 December 2020

Transgenic mice expressing a mutant keratin 10 gene reveal the likely genetic basis for epidermolytic hyperkeratosis

1 reference

12 December 2020

A Novel Locus of Ectodermal Dysplasia Maps to Chromosome 10q24.32–q25.1

1 reference

12 December 2020

Descent graphs in pedigree analysis: applications to haplotyping, location scores, and marker-sharing statistics

1 reference

12 December 2020

Family with "pure" hair-nail ectodermal dysplasia

1 reference

12 December 2020

Computer programs for multilocus haplotyping of general pedigrees.

1 reference

12 December 2020

The human type I keratin gene family: characterization of new hair follicle specific members and evaluation of the chromosome 17q21.2 gene domain

1 reference

12 December 2020

Faster sequential genetic linkage computations

1 reference

12 December 2020

Incorrect specification of marker allele frequencies: effects on linkage analysis

1 reference

12 December 2020

Pili torti and onychodysplasia. Report of a previously undescribed hidrotic ectodermal dysplasia

1 reference

12 December 2020

Mutations in the rod domains of keratins 1 and 10 in epidermolytic hyperkeratosis

1 reference

12 December 2020

PedCheck: a program for identification of genotype incompatibilities in linkage analysis

1 reference

12 December 2020

Towards a new classification of ectodermal dysplasias.

1 reference

12 December 2020

A combined linkage-physical map of the human genome

1 reference

12 December 2020

The genetic basis of epidermolytic hyperkeratosis: a disorder of differentiation-specific epidermal keratin genes.

1 reference

12 December 2020

Initial sequencing and analysis of the human genome

1 reference

12 December 2020

Allegro, a new computer program for multipoint linkage analysis

1 reference

12 December 2020

Hypotrichosis and nail dysplasia: a novel hidrotic ectodermal dysplasia

1 reference

12 December 2020

10.1111/J.1365-2133.2006.07509.X

Identifiers

DOI

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17107387%20AND%20SRC:MED&resulttype=core&format=json

21 December 2019

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21 December 2019

PubMed publication ID

17107387

1 reference