(Q64968639)

2 July 2019

title

A locus for hereditary hypotrichosis localized to human chromosome 18q21.1. (English)

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2 July 2019

author

Sajid Malik

4

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2 July 2019

Suzanne M. Leal

8

object named as

Suzanne M Leal

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2 July 2019

author name string

Muhammad Arshad Rafique

1

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2 July 2019

Muhammad Ansar

2

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2 July 2019

Syed Muhammad Jamal

3

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2 July 2019

Muhammad Sohail

5

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2 July 2019

Mohammad Faiyaz-Ul-Haque

6

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2 July 2019

Sayedul Haque

7

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2 July 2019

Wasim Ahmad

9

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2 July 2019

publication date

1 August 2003

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2 July 2019

European Journal of Human Genetics

published in

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2 July 2019

volume

11

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2 July 2019

page(s)

623-628

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2 July 2019

issue

8

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2 July 2019

https://scigraph.springernature.com/pub.10.1038/sj.ejhg.5201005

exact match

0 references

cites work

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Hereditary hypotrichosis simplex of the scalp. Evidence for autosomal dominant inheritance

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A gene for autosomal dominant hypohidrotic ectodermal dysplasia (EDA3) maps to chromosome 2q11-q13

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Pemphigus vulgaris antigen is a desmosomal desmoglein

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12 December 2020

A gene for monilethrix is closely linked to the type II keratin gene cluster at 12q13

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Marie Unna hereditary hypotrichosis

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12 December 2020

Marie Unna hereditary hypotrichosis gene maps to human chromosome 8p21 near hairless

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Netherton's syndrome: a syndrome of elevated IgE and characteristic skin and hair findings

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Human desmocollin 1 (Dsc1) is an autoantigen for the subcorneal pustular dermatosis type of IgA pemphigus

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A unique case of trichorrhexis nodosa; bamboo hairs

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A variable monilethrix phenotype associated with a novel mutation, Glu402Lys, in the helix termination motif of the type II hair keratin hHb1.

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Cloning of the gene for human pemphigus vulgaris antigen (desmoglein 3), a desmosomal cadherin. Characterization of the promoter region and identification of a keratinocyte-specific cis-element

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An autosomal dominant form of hereditary hypotrichosis simplex maps to 18p11.32-p11.23 in an Italian family

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Assignment of the Gene for a New Hereditary Nail Disorder, Isolated Congenital Nail Dysplasia, to Chromosome 17p13

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A gene for universal congenital alopecia maps to chromosome 8p21-22

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A missense mutation in the zinc-finger domain of the human hairless gene underlies congenital atrichia in a family of Irish travellers

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The gene responsible for Clouston hidrotic ectodermal dysplasia maps to the pericentromeric region of chromosome 13q

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12 December 2020

A gene for hypotrichosis simplex of the scalp maps to chromosome 6p21.3.

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12 December 2020

Tandem arrangement of the closely linked desmoglein genes on human chromosome 18

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12 December 2020

Human globin locus activation region (LAR): role in temporal control

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The desmocollins of human foreskin epidermis: identification and chromosomal assignment of a third gene and expression patterns of the three isoforms

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12 December 2020

Hereditary hypotrichosis simplex of the scalp

1 reference

Crossref

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201005

7 January 2021

inferred from DOI database lookup

Identifiers

DOI

10.1038/SJ.EJHG.5201005

1 reference

2 July 2019

PMCID

6157268

1 reference

2 July 2019

PubMed ID

12891384

1 reference

2 July 2019