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Paradoxical frequencies of recessive disorders in Ashkenazic Jews
scientific article published on 01 January 1971
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instance of
scholarly article
1 reference
stated in
Europe PubMed Central
PubMed publication ID
5090327
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:5090327%20AND%20SRC:MED&resulttype=core&format=json
retrieved
12 October 2019
title
Paradoxical frequencies of recessive disorders in Ashkenazic Jews
(English)
1 reference
stated in
Europe PubMed Central
PubMed publication ID
5090327
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:5090327%20AND%20SRC:MED&resulttype=core&format=json
retrieved
12 October 2019
main subject
medical genetics
1 reference
stated in
Europe PubMed Central
PubMed publication ID
5090327
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A5090327
retrieved
15 April 2023
recessive genes
1 reference
stated in
Europe PubMed Central
PubMed publication ID
5090327
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A5090327
retrieved
15 April 2023
author name string
R. A. Meals
series ordinal
1
1 reference
stated in
Europe PubMed Central
PubMed publication ID
5090327
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A5090327
retrieved
15 April 2023
language of work or name
English
1 reference
stated in
National Center for Biotechnology Information
PubMed publication ID
5090327
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/esummary.fcgi?db=pubmed&retmode=json&id=5090327
retrieved
15 April 2023
publication date
1 January 1971
1 reference
stated in
Europe PubMed Central
PubMed publication ID
5090327
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:5090327%20AND%20SRC:MED&resulttype=core&format=json
retrieved
12 October 2019
full work available at URL
https://api.elsevier.com/content/article/PII:0021968171901305?httpAccept=text/xml
1 reference
stated in
Crossref
DOI
10.1016/0021-9681(71)90130-5
reference URL
https://api.crossref.org/works/10.1016/0021-9681(71)90130-5
retrieved
15 April 2023
https://api.elsevier.com/content/article/PII:0021968171901305?httpAccept=text/plain
1 reference
stated in
Crossref
DOI
10.1016/0021-9681(71)90130-5
reference URL
https://api.crossref.org/works/10.1016/0021-9681(71)90130-5
retrieved
15 April 2023
published in
Journal of Chronic Diseases
1 reference
stated in
Europe PubMed Central
PubMed publication ID
5090327
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:5090327%20AND%20SRC:MED&resulttype=core&format=json
retrieved
12 October 2019
volume
23
1 reference
stated in
Europe PubMed Central
PubMed publication ID
5090327
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:5090327%20AND%20SRC:MED&resulttype=core&format=json
retrieved
12 October 2019
issue
8
1 reference
stated in
Europe PubMed Central
PubMed publication ID
5090327
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:5090327%20AND%20SRC:MED&resulttype=core&format=json
retrieved
12 October 2019
page(s)
547-558
1 reference
stated in
Europe PubMed Central
PubMed publication ID
5090327
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:5090327%20AND%20SRC:MED&resulttype=core&format=json
retrieved
12 October 2019
cites work
Tay-Sachs Disease: Generalized Absence of a Beta-D- N -Acetylhexosaminidase Component
series ordinal
5
1 reference
stated in
Crossref
DOI
10.1016/0021-9681(71)90130-5
reference URL
https://api.crossref.org/works/10.1016/0021-9681(71)90130-5
retrieved
15 April 2023
GAUCHER'S DISEASE. HEREDITARY TRANSMISSION AND RACIAL DISTRIBUTION
series ordinal
10
1 reference
stated in
Crossref
DOI
10.1016/0021-9681(71)90130-5
reference URL
https://api.crossref.org/works/10.1016/0021-9681(71)90130-5
retrieved
15 April 2023
METABOLISM OF GLUCOCEREBROSIDES. II. EVIDENCE OF AN ENZYMATIC DEFICIENCY IN GAUCHER'S DISEASE.
series ordinal
11
1 reference
stated in
Crossref
DOI
10.1016/0021-9681(71)90130-5
reference URL
https://api.crossref.org/works/10.1016/0021-9681(71)90130-5
retrieved
15 April 2023
The metabolism of sphingomyelin. II. Evidence of an enzymatic deficiency in Niemann-Pick diseae
series ordinal
14
1 reference
stated in
Crossref
DOI
10.1016/0021-9681(71)90130-5
reference URL
https://api.crossref.org/works/10.1016/0021-9681(71)90130-5
retrieved
15 April 2023
SPONGY DEGENERATION OF THE CENTRAL NERVOUS SYSTEM IN INFANCY.
series ordinal
21
1 reference
stated in
Crossref
DOI
10.1016/0021-9681(71)90130-5
reference URL
https://api.crossref.org/works/10.1016/0021-9681(71)90130-5
retrieved
15 April 2023
The syndrome of congenital telangiectaticerythema and stunted growth
series ordinal
22
1 reference
stated in
Crossref
DOI
10.1016/0021-9681(71)90130-5
reference URL
https://api.crossref.org/works/10.1016/0021-9681(71)90130-5
retrieved
15 April 2023
Chromosomal breakage and acute leukemia in congenital telangiectatic erythema and stunted growth
series ordinal
23
1 reference
stated in
Crossref
DOI
10.1016/0021-9681(71)90130-5
reference URL
https://api.crossref.org/works/10.1016/0021-9681(71)90130-5
retrieved
15 April 2023
The ethnic distribution of disease in the United States
series ordinal
33
1 reference
stated in
Crossref
DOI
10.1016/0021-9681(71)90130-5
reference URL
https://api.crossref.org/works/10.1016/0021-9681(71)90130-5
retrieved
15 April 2023
Autosomal deletion mapping in man
series ordinal
36
1 reference
stated in
Crossref
DOI
10.1016/0021-9681(71)90130-5
reference URL
https://api.crossref.org/works/10.1016/0021-9681(71)90130-5
retrieved
15 April 2023
Population dynamics of Tay-Sachs disease. I. Reproductive fitness and selection
series ordinal
38
1 reference
stated in
Crossref
DOI
10.1016/0021-9681(71)90130-5
reference URL
https://api.crossref.org/works/10.1016/0021-9681(71)90130-5
retrieved
15 April 2023
"Genetic Drift" in an Italian Population
series ordinal
40
1 reference
stated in
Crossref
DOI
10.1016/0021-9681(71)90130-5
reference URL
https://api.crossref.org/works/10.1016/0021-9681(71)90130-5
retrieved
15 April 2023
The founder effect and deleterious genes
series ordinal
41
1 reference
stated in
Crossref
DOI
10.1016/0021-9681(71)90130-5
reference URL
https://api.crossref.org/works/10.1016/0021-9681(71)90130-5
retrieved
15 April 2023
Inherited neurologic diseases of Ashkenazic Jewry: demographic data suggesting non-random gene frequencies
series ordinal
43
1 reference
stated in
Crossref
DOI
10.1016/0021-9681(71)90130-5
reference URL
https://api.crossref.org/works/10.1016/0021-9681(71)90130-5
retrieved
15 April 2023
A genetical analysis of thirty families with Wilson's disease (hepatolenticular degeneration)
series ordinal
44
1 reference
stated in
Crossref
DOI
10.1016/0021-9681(71)90130-5
reference URL
https://api.crossref.org/works/10.1016/0021-9681(71)90130-5
retrieved
15 April 2023
A clinical, genetic and biochemical study of familial dysautonomia in Israel
series ordinal
17
1 reference
stated in
Crossref
DOI
10.1016/0021-9681(71)90130-5
reference URL
https://api.crossref.org/works/10.1016/0021-9681(71)90130-5
retrieved
12 December 2023
Identifiers
DOI
10.1016/0021-9681(71)90130-5
1 reference
stated in
Europe PubMed Central
PubMed publication ID
5090327
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:5090327%20AND%20SRC:MED&resulttype=core&format=json
retrieved
12 October 2019
PubMed publication ID
5090327
1 reference
stated in
Europe PubMed Central
PubMed publication ID
5090327
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:5090327%20AND%20SRC:MED&resulttype=core&format=json
retrieved
12 October 2019
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