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Down syndrome in association with features of the androgen insensitivity syndrome.
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scholarly article
1 reference
stated in
Europe PubMed Central
PMC publication ID
1050665
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8818943%20AND%20SRC:MED&resulttype=core&format=json
retrieved
19 October 2019
title
Down syndrome in association with features of the androgen insensitivity syndrome
(English)
1 reference
stated in
Europe PubMed Central
PMC publication ID
1050665
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8818943%20AND%20SRC:MED&resulttype=core&format=json
retrieved
19 October 2019
main subject
Down syndrome
1 reference
based on heuristic
inferred from title
author
Andrew Green
series ordinal
4
1 reference
stated in
Europe PubMed Central
PMC publication ID
1050665
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8818943%20AND%20SRC:MED&resulttype=core&format=json
retrieved
19 October 2019
author name string
R M Viner
series ordinal
1
1 reference
stated in
Europe PubMed Central
PMC publication ID
1050665
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8818943%20AND%20SRC:MED&resulttype=core&format=json
retrieved
19 October 2019
N Shimura
series ordinal
2
1 reference
stated in
Europe PubMed Central
PMC publication ID
1050665
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8818943%20AND%20SRC:MED&resulttype=core&format=json
retrieved
19 October 2019
B D Brown
series ordinal
3
1 reference
stated in
Europe PubMed Central
PMC publication ID
1050665
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8818943%20AND%20SRC:MED&resulttype=core&format=json
retrieved
19 October 2019
I A Hughes
series ordinal
5
1 reference
stated in
Europe PubMed Central
PMC publication ID
1050665
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8818943%20AND%20SRC:MED&resulttype=core&format=json
retrieved
19 October 2019
language of work or name
English
0 references
publication date
1 July 1996
1 reference
stated in
Europe PubMed Central
PMC publication ID
1050665
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8818943%20AND%20SRC:MED&resulttype=core&format=json
retrieved
19 October 2019
published in
Journal of Medical Genetics
1 reference
stated in
Europe PubMed Central
PMC publication ID
1050665
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8818943%20AND%20SRC:MED&resulttype=core&format=json
retrieved
19 October 2019
volume
33
1 reference
stated in
Europe PubMed Central
PMC publication ID
1050665
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8818943%20AND%20SRC:MED&resulttype=core&format=json
retrieved
19 October 2019
issue
7
1 reference
stated in
Europe PubMed Central
PMC publication ID
1050665
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8818943%20AND%20SRC:MED&resulttype=core&format=json
retrieved
19 October 2019
page(s)
574-577
1 reference
stated in
Europe PubMed Central
PMC publication ID
1050665
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8818943%20AND%20SRC:MED&resulttype=core&format=json
retrieved
19 October 2019
cites work
Genetic basis of endocrine disease. 4. The spectrum of mutations in the androgen receptor gene that causes androgen resistance
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=1050665
retrieved
28 July 2018
Mutational screening of the Wilms's tumour gene, WT1, in males with genital abnormalities
1 reference
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PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1050665
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28 July 2018
SRY and sex determination in mammals
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=1050665
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28 July 2018
An unusual member of the nuclear hormone receptor superfamily responsible for X-linked adrenal hypoplasia congenita
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=1050665
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28 July 2018
Campomelic dysplasia and autosomal sex reversal caused by mutations in an SRY-related gene
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=1050665
retrieved
28 July 2018
A dosage sensitive locus at chromosome Xp21 is involved in male to female sex reversal
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=1050665
retrieved
28 July 2018
Down's syndrome in the male. Reproductive pathology and meiotic studies
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=1050665
retrieved
28 July 2018
Male pseudohermaphroditism in a child with Down's 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=1050665
retrieved
28 July 2018
Augmentation of androgen-receptor binding in vitro: studies in normals and patients with androgen insensitivity
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=1050665
retrieved
28 July 2018
Adolescent development in males with Down 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=1050665
retrieved
28 July 2018
Gonadal function in patients with Down 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=1050665
retrieved
28 July 2018
Fertility in a male with trisomy 21
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=1050665
retrieved
28 July 2018
Androgen resistance--the clinical and molecular spectrum
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=1050665
retrieved
28 July 2018
Sex reversal in a child with a 46,X,Yp+ karyotype: support for the existence of a gene(s), located in distal Xp, involved in testis formation
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=1050665
retrieved
28 July 2018
Androgen receptor gene mutations identified by SSCP in fourteen subjects with androgen insensitivity 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=1050665
retrieved
28 July 2018
LH-RH testing in men with Down's 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=1050665
retrieved
28 July 2018
Studies of the androgen receptor in dispersed fibroblasts: investigation of patients with androgen insensitivity.
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=1050665
retrieved
30 October 2018
Hypospadias and urethral abnormalities in Down syndrome
1 reference
stated in
PubMed
reference URL
https://pubmed.ncbi.nlm.nih.gov/8818943
retrieved
12 December 2020
based on heuristic
inferred from PubMed ID database lookup
Androgen insensitivity syndrome
1 reference
stated in
PubMed
reference URL
https://pubmed.ncbi.nlm.nih.gov/8818943
retrieved
12 December 2020
based on heuristic
inferred from PubMed ID database lookup
Patient with Down's syndrome and male pseudohermaphroditism with a 47, XY, plus21 karyotype
1 reference
stated in
PubMed
reference URL
https://pubmed.ncbi.nlm.nih.gov/8818943
retrieved
12 December 2020
based on heuristic
inferred from PubMed ID database lookup
Identifiers
DOI
10.1136/JMG.33.7.574
1 reference
stated in
Europe PubMed Central
PMC publication ID
1050665
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8818943%20AND%20SRC:MED&resulttype=core&format=json
retrieved
19 October 2019
PMC publication ID
1050665
1 reference
stated in
Europe PubMed Central
PMC publication ID
1050665
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8818943%20AND%20SRC:MED&resulttype=core&format=json
retrieved
19 October 2019
PubMed publication ID
8818943
1 reference
stated in
Europe PubMed Central
PMC publication ID
1050665
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8818943%20AND%20SRC:MED&resulttype=core&format=json
retrieved
19 October 2019
ResearchGate publication ID
14386276
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