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The Sabinas syndrome
scientific article published on November 1, 1981
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Statements
instance of
scholarly article
1 reference
stated in
Europe PubMed Central
PMC publication ID
1685163
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7325159%20AND%20SRC:MED&resulttype=core&format=json
retrieved
15 October 2019
title
The Sabinas syndrome
(English)
1 reference
stated in
Europe PubMed Central
PMC publication ID
1685163
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7325159%20AND%20SRC:MED&resulttype=core&format=json
retrieved
15 October 2019
main subject
recessive genes
1 reference
stated in
Europe PubMed Central
PubMed publication ID
7325159
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A7325159
retrieved
5 May 2024
author name string
R. R. Howell
series ordinal
1
1 reference
stated in
Europe PubMed Central
PubMed publication ID
7325159
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A7325159
retrieved
5 May 2024
A. I. Arbisser
series ordinal
2
1 reference
stated in
Europe PubMed Central
PubMed publication ID
7325159
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A7325159
retrieved
5 May 2024
D. S. Parsons
series ordinal
3
1 reference
stated in
Europe PubMed Central
PubMed publication ID
7325159
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A7325159
retrieved
5 May 2024
C. I. Scott
series ordinal
4
1 reference
stated in
Europe PubMed Central
PubMed publication ID
7325159
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A7325159
retrieved
5 May 2024
U. Fraustadt
series ordinal
5
1 reference
stated in
Europe PubMed Central
PubMed publication ID
7325159
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A7325159
retrieved
5 May 2024
W. R. Collie
series ordinal
6
1 reference
stated in
Europe PubMed Central
PubMed publication ID
7325159
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A7325159
retrieved
5 May 2024
R. N. Marshall
series ordinal
7
1 reference
stated in
Europe PubMed Central
PubMed publication ID
7325159
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A7325159
retrieved
5 May 2024
O. C. Ibarra
series ordinal
8
1 reference
stated in
Europe PubMed Central
PubMed publication ID
7325159
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A7325159
retrieved
5 May 2024
language of work or name
English
0 references
publication date
1 November 1981
1 reference
stated in
Europe PubMed Central
PMC publication ID
1685163
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7325159%20AND%20SRC:MED&resulttype=core&format=json
retrieved
15 October 2019
full work available at URL
https://www.ncbi.nlm.nih.gov/pmc/articles/pmid/7325159/?tool=EBI
file format
HTML
online access status
open access
content deliverer
PubMed Central
1 reference
stated in
Europe PubMed Central
PubMed publication ID
7325159
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A7325159
retrieved
5 May 2024
https://www.ncbi.nlm.nih.gov/pmc/articles/pmid/7325159/pdf/?tool=EBI
file format
Portable Document Format
online access status
open access
content deliverer
PubMed Central
1 reference
stated in
Europe PubMed Central
PubMed publication ID
7325159
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A7325159
retrieved
5 May 2024
https://europepmc.org/articles/PMC1685163
file format
HTML
online access status
open access
content deliverer
Europe PubMed Central
1 reference
stated in
Europe PubMed Central
PubMed publication ID
7325159
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A7325159
retrieved
5 May 2024
https://europepmc.org/articles/PMC1685163?pdf=render
file format
Portable Document Format
online access status
open access
content deliverer
Europe PubMed Central
1 reference
stated in
Europe PubMed Central
PubMed publication ID
7325159
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A7325159
retrieved
5 May 2024
published in
American Journal of Human Genetics
1 reference
stated in
Europe PubMed Central
PMC publication ID
1685163
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7325159%20AND%20SRC:MED&resulttype=core&format=json
retrieved
15 October 2019
volume
33
1 reference
stated in
Europe PubMed Central
PMC publication ID
1685163
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7325159%20AND%20SRC:MED&resulttype=core&format=json
retrieved
15 October 2019
issue
6
1 reference
stated in
Europe PubMed Central
PMC publication ID
1685163
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7325159%20AND%20SRC:MED&resulttype=core&format=json
retrieved
15 October 2019
page(s)
957-967
1 reference
stated in
Europe PubMed Central
PMC publication ID
1685163
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7325159%20AND%20SRC:MED&resulttype=core&format=json
retrieved
15 October 2019
cites work
Sibs with mental and physical retardation and trichorrhexis nodosa with abnormal amino acid composition of the hair
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1685163
retrieved
28 September 2017
Menkes disease: a biochemical abnormality in cultured human fibroblasts
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1685163
retrieved
28 September 2017
A Congenital Hair Defect: Trichoschisis With Alternating Birefringence and Low Sulfur Content
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1685163
retrieved
30 May 2018
Proteins of normal hair and of cysteine-deficient hair from mentally retarded siblings
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1685163
retrieved
30 May 2018
"Brittle" hair with short stature, intellectual impairment and decreased fertility: an autosomal recessive syndrome in an Amish kindred
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1685163
retrieved
30 May 2018
A familial syndrome of deafness, alopecia, and hypogonadism.
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1685163
retrieved
30 May 2018
Autosomal recessive onychotrichodysplasia, chronic neutropenia and mild mental retardation. Delineation of the syndrome
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1685163
retrieved
30 May 2018
Alopecia congenita: the incomplete dominant form of inheritance with varying expressivity
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1685163
retrieved
28 November 2018
Infantile metachromatic leukodystrophy
1 reference
stated in
PubMed
reference URL
https://pubmed.ncbi.nlm.nih.gov/7325159
retrieved
12 December 2020
based on heuristic
inferred from PubMed ID database lookup
Ectodermal dysplasia
1 reference
stated in
PubMed
reference URL
https://pubmed.ncbi.nlm.nih.gov/7325159
retrieved
12 December 2020
based on heuristic
inferred from PubMed ID database lookup
Integration of Pulsatile Gonadotropin Secretion by Timed Urinary Measurements: An Accurate and Sensitive 3-Hour Test
1 reference
stated in
PubMed
reference URL
https://pubmed.ncbi.nlm.nih.gov/7325159
retrieved
12 December 2020
based on heuristic
inferred from PubMed ID database lookup
Computerized data analysis of amino acids in physiologic fluids
1 reference
stated in
PubMed
reference URL
https://pubmed.ncbi.nlm.nih.gov/7325159
retrieved
12 December 2020
based on heuristic
inferred from PubMed ID database lookup
Identifiers
PMC publication ID
1685163
1 reference
stated in
Europe PubMed Central
PMC publication ID
1685163
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7325159%20AND%20SRC:MED&resulttype=core&format=json
retrieved
15 October 2019
PubMed publication ID
7325159
1 reference
stated in
Europe PubMed Central
PMC publication ID
1685163
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7325159%20AND%20SRC:MED&resulttype=core&format=json
retrieved
15 October 2019
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