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English
Congenital disorders of hypopigmentation.
scientific article published on March 1995
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instance of
scholarly article
1 reference
stated in
Europe PubMed Central
PubMed publication ID
7742237
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7742237%20AND%20SRC:MED&resulttype=core&format=json
retrieved
24 October 2019
review article
1 reference
stated in
Europe PubMed Central
title
Congenital disorders of hypopigmentation
(English)
1 reference
stated in
Europe PubMed Central
PubMed publication ID
7742237
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7742237%20AND%20SRC:MED&resulttype=core&format=json
retrieved
24 October 2019
main subject
congenital disorder
0 references
author
Seth J Orlow
series ordinal
1
1 reference
stated in
Europe PubMed Central
PubMed publication ID
7742237
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7742237%20AND%20SRC:MED&resulttype=core&format=json
retrieved
24 October 2019
author name string
Orlow SJ
series ordinal
1
1 reference
stated in
Europe PubMed Central
PubMed publication ID
7742237
retrieved
21 September 2017
publication date
1 March 1995
1 reference
stated in
Europe PubMed Central
PubMed publication ID
7742237
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7742237%20AND%20SRC:MED&resulttype=core&format=json
retrieved
24 October 2019
published in
Seminars in dermatology
1 reference
stated in
Europe PubMed Central
PubMed publication ID
7742237
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7742237%20AND%20SRC:MED&resulttype=core&format=json
retrieved
24 October 2019
volume
14
1 reference
stated in
Europe PubMed Central
PubMed publication ID
7742237
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7742237%20AND%20SRC:MED&resulttype=core&format=json
retrieved
24 October 2019
issue
1
1 reference
stated in
Europe PubMed Central
PubMed publication ID
7742237
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7742237%20AND%20SRC:MED&resulttype=core&format=json
retrieved
24 October 2019
page(s)
27-32
1 reference
stated in
Europe PubMed Central
PubMed publication ID
7742237
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7742237%20AND%20SRC:MED&resulttype=core&format=json
retrieved
24 October 2019
cites work
Familial white skin spotting (piebaldness) ("partial albinism") with white forelock
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS1085-5629%2805%2980036-7
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Partial albinism. Nine cases in six generations
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS1085-5629%2805%2980036-7
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Piebaldism
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS1085-5629%2805%2980036-7
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Expansion and contraction of hypomelanotic areas in human piebaldism
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS1085-5629%2805%2980036-7
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Tyrosinase-positive melanocyte distribution and induction of pigmentation in human piebald skin
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS1085-5629%2805%2980036-7
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Congenital Circumscribed Hypomelanosis: A Characterization Based on Electron Microscopic Study of Tuberous Sclerosis, Nevus Depigmentosus, and Piebaldism
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS1085-5629%2805%2980036-7
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Upper limb involvement in the Klein-Waardenburg syndrome
1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS1085-5629%2805%2980036-7
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Mutations in the PAX3 gene causing Waardenburg syndrome type 1 and type 2
1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS1085-5629%2805%2980036-7
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
The association of Waardenburg syndrome and Hirschsprung megacolon
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS1085-5629%2805%2980036-7
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Waardenburg's syndrome associated with total aganglionosis
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS1085-5629%2805%2980036-7
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Hypomelanosis of Ito: diagnostic criteria and report of 41 cases
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS1085-5629%2805%2980036-7
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Pigmentary abnormalities and mosaicism for chromosomal aberration: association with clinical features similar to hypomelanosis of Ito.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS1085-5629%2805%2980036-7
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Molecular analysis of type I-A (tyrosinase negative) oculocutaneous albinism
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS1085-5629%2805%2980036-7
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
The Tanzanian human albino skin. Natural history
1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS1085-5629%2805%2980036-7
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7 January 2021
based on heuristic
inferred from DOI database lookup
The mouse pink-eyed dilution gene: association with human Prader-Willi and Angelman syndromes
1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS1085-5629%2805%2980036-7
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
A gene for the mouse pink-eyed dilution locus and for human type II oculocutaneous albinism
1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS1085-5629%2805%2980036-7
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
The mouse pink-eyed dilution locus: a model for aspects of Prader-Willi syndrome, Angelman syndrome, and a form of hypomelanosis of Ito.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS1085-5629%2805%2980036-7
retrieved
7 January 2021
based on heuristic
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The Hermansky–Pudlak Syndrome
1 reference
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Crossref
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https://api.crossref.org/works/10.1016%2FS1085-5629%2805%2980036-7
retrieved
7 January 2021
based on heuristic
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The Chediak-Higashi syndrome: formation of giant melanosomes and the basis of hypopigmentation
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS1085-5629%2805%2980036-7
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Chediak-Higashi syndrome in a black child
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS1085-5629%2805%2980036-7
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
A syndrome associating partial albinism and immunodeficiency
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS1085-5629%2805%2980036-7
retrieved
7 January 2021
based on heuristic
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Identifiers
DOI
10.1016/S1085-5629(05)80036-7
1 reference
stated in
Europe PubMed Central
PubMed publication ID
7742237
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7742237%20AND%20SRC:MED&resulttype=core&format=json
retrieved
24 October 2019
PubMed publication ID
7742237
1 reference
stated in
Europe PubMed Central
PubMed publication ID
7742237
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7742237%20AND%20SRC:MED&resulttype=core&format=json
retrieved
24 October 2019
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