(Q34304223)

reason for preferred rank

1 August 2017

title

Mapping of the congenital generalized hypertrichosis locus to chromosome Xq24–q27.1 (English)

1 reference

29 July 2024

Mapping of the congenital generalized hypertrichosis locus to chromosome Xq24-q27.1 (English)

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A7663516

29 July 2024

0 references

1 reference

1

L. E. Figuera

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A7663516

29 July 2024

5

P. I. Patel

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A7663516

29 July 2024

author name string

M. Pandolfo

2

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A7663516

29 July 2024

P. W. Dunne

3

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A7663516

29 July 2024

J. M. Cantú

4

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A7663516

29 July 2024

language of work or name

English

0 references

publication date

1 June 1995

1 reference

full work available at URL

1 August 2017

http://www.nature.com/articles/ng0695-202

1 reference

http://www.nature.com/articles/ng0695-202.pdf

29 July 2024

file format

Portable Document Format

1 reference

29 July 2024

1 reference

1 August 2017

volume

10

1 reference

1 August 2017

issue

2

1 reference

1 August 2017

page(s)

202-207

1 reference

Mosaicism in human skin. Understanding the patterns and mechanisms

1 August 2017

cites work

1 reference

https://api.crossref.org/works/10.1038%2FNG0695-202

The 1993-94 Généthon human genetic linkage map

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNG0695-202

A second-generation linkage map of the human genome

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNG0695-202

A linkage map of microsatellite markers on the human X chromosome

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNG0695-202

FGF5 as a regulator of the hair growth cycle: evidence from targeted and spontaneous mutations

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNG0695-202

Congenital Hypertrichosis Lanuginosa

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNG0695-202

Naevocytic naevi as an atavism; their relationship to melanoma risk

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNG0695-202

A new form of hypertrichosis inherited as an X-linked dominant trait

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNG0695-202

7 January 2021

Localisation of the gene for Hunter syndrome on the long arm of X chromosome

1 reference

https://api.crossref.org/works/10.1038%2FNG0695-202

7 January 2021

The epidermis: rising to the surface

1 reference

https://api.crossref.org/works/10.1038%2FNG0695-202

7 January 2021

The secret life of the hair follicle

1 reference

https://api.crossref.org/works/10.1038%2FNG0695-202

7 January 2021

Distribution of Epidermal Growth Factor Receptors in Rat Tissues During Embryonic Skin Development, Hair Formation, and the Adult Hair Growth Cycle

1 reference

https://api.crossref.org/works/10.1038%2FNG0695-202

7 January 2021

Transgenic mice as a model to study the role of TGF-beta-related molecules in hair follicles

1 reference

https://api.crossref.org/works/10.1038%2FNG0695-202

7 January 2021

Hypertrichosis with hereditary gingival hyperplasia

1 reference

https://api.crossref.org/works/10.1038%2FNG0695-202

7 January 2021

de Lange syndrome: a clinical review of 310 individuals

1 reference

https://api.crossref.org/works/10.1038%2FNG0695-202

7 January 2021

The Coffin-Siris syndrome: report of a family and further delineation.

1 reference

https://api.crossref.org/works/10.1038%2FNG0695-202

7 January 2021

A distinct osteochondrodysplasia with hypertrichosis- Individualization of a probable autosomal recessive entity.

1 reference

https://api.crossref.org/works/10.1038%2FNG0695-202

7 January 2021

Lawrence-Seip syndrome

1 reference

https://api.crossref.org/works/10.1038%2FNG0695-202

7 January 2021

A syndrome of severe midface retraction, multiple skull anomalies, clubfeet, and cardiac and renal malformations in sibs

1 reference

https://api.crossref.org/works/10.1038%2FNG0695-202

7 January 2021

Craniofacial dysostosis, patent ductus arteriosus, hypertrichosis, hypoplasia of labia majora, dental and eye anomalies-a new syndrome?

1 reference

https://api.crossref.org/works/10.1038%2FNG0695-202

7 January 2021

Prepubertal hypertrichosis: normal or abnormal?

1 reference

https://api.crossref.org/works/10.1038%2FNG0695-202

7 January 2021

Familial Supernumerary Nipples and Breasts

1 reference

https://api.crossref.org/works/10.1038%2FNG0695-202

7 January 2021

Use of cyclosporin A in establishing Epstein-Barr virus-transformed human lymphoblastoid cell lines

1 reference

https://api.crossref.org/works/10.1038%2FNG0695-202

7 January 2021

Mapping of the gene for X-chromosomal split-hand/split-foot anomaly to Xq26-q26.1.

1 reference

https://api.crossref.org/works/10.1038%2FNG0695-202

7 January 2021

DNA duplication associated with Charcot-Marie-Tooth disease type 1A

1 reference

https://api.crossref.org/works/10.1038%2FNG0695-202

7 January 2021

Cytogenetics and Cell Genetics

12

67

296

HF Willard

1994

1 reference

Hypertrichosis lanuginosa in a mother and son

29 July 2024

26

1 reference

29 July 2024

Identifiers

DOI

10.1038/NG0695-202

1 reference

Dimensions Publication ID

1 August 2017

1011725312

0 references

1 reference