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Growing interest in overgrowth
scientific article published in March 1998
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Statements
instance of
scholarly article
1 reference
stated in
Europe PubMed Central
PMCID
1717479
retrieved
13 November 2017
title
Growing interest in overgrowth
(English)
1 reference
stated in
Europe PubMed Central
PMCID
1717479
retrieved
13 November 2017
author name string
Cole T
series ordinal
1
1 reference
stated in
Europe PubMed Central
PMCID
1717479
retrieved
13 November 2017
language of work or name
English
0 references
publication date
1 March 1998
1 reference
stated in
Europe PubMed Central
PMCID
1717479
retrieved
13 November 2017
published in
Archives of Disease in Childhood
1 reference
stated in
Europe PubMed Central
PMCID
1717479
retrieved
13 November 2017
volume
78
1 reference
stated in
Europe PubMed Central
PMCID
1717479
retrieved
13 November 2017
issue
3
1 reference
stated in
Europe PubMed Central
PMCID
1717479
retrieved
13 November 2017
page(s)
200-204
1 reference
stated in
Europe PubMed Central
PMCID
1717479
retrieved
13 November 2017
cites work
CEREBRAL GIGANTISM IN CHILDHOOD. A SYNDROME OF EXCESSIVELY RAPID GROWTH AND ACROMEGALIC FEATURES AND A NONPROGRESSIVE NEUROLOGIC DISORDER.
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=1717479
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25 May 2018
Autosomal dominant inheritance of Weaver syndrome
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PubMed Central
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retrieved
25 May 2018
No evidence for uniparental disomy as a common cause of Sotos syndrome
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PubMed Central
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https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1717479
retrieved
25 May 2018
An imprinted gene p57KIP2 is mutated in Beckwith-Wiedemann syndrome
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=1717479
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25 May 2018
Generalized lipodystrophy, congenital and acquired (lipoatrophy).
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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=1717479
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25 May 2018
Mutations in GPC3, a glypican gene, cause the Simpson-Golabi-Behmel overgrowth syndrome
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=1717479
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25 May 2018
Disruption of insulin-like growth factor 2 imprinting in Beckwith-Wiedemann syndrome
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PubMed Central
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25 May 2018
Clinical features and natural history of Beckwith-Wiedemann syndrome: presentation of 74 new cases
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PubMed Central
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25 May 2018
Sotos syndrome: a study of the diagnostic criteria and natural history
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PubMed Central
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25 May 2018
Fibrillin-2 (FBN2) mutations result in the Marfan-like disorder, congenital contractural arachnodactyly
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PubMed Central
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25 May 2018
The syndromes of Marshall and Weaver.
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PubMed Central
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25 May 2018
Exomphalos-Macroglossia-Gigantism Syndrome in Jamaican Infants
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25 May 2018
A comprehensive and critical assessment of overgrowth and overgrowth syndromes
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PubMed Central
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25 May 2018
Familial Wiedemann-Beckwith syndrome and a second Wilms tumor locus both map to 11p15.5.
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PubMed Central
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25 May 2018
Simpson-Golabi-Behmel syndrome associated with renal dysplasia and embryonal tumor: localization of the gene to Xqcen-q21.
1 reference
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PubMed Central
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https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1717479
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25 May 2018
Identification of a mutation in the gene encoding the alpha subunit of the stimulatory G protein of adenylyl cyclase in McCune-Albright syndrome
1 reference
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PubMed Central
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https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1717479
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25 May 2018
Macrocephaly in association with unusual cutaneous angiomatosis
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PubMed Central
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25 May 2018
Marfan syndrome caused by a recurrent de novo missense mutation in the fibrillin gene
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PubMed Central
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27 July 2018
Autism and macrocephaly.
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PubMed Central
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https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1717479
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15 August 2018
Human KVLQT1 gene shows tissue-specific imprinting and encompasses Beckwith-Wiedemann syndrome chromosomal rearrangements.
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=1717479
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15 August 2018
Somatic overgrowth associated with overexpression of insulin-like growth factor II.
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=1717479
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15 August 2018
Language and behavior in children with Sotos syndrome.
1 reference
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PubMed Central
reference URL
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15 August 2018
Birth weight and the incidence of childhood cancer.
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PubMed Central
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15 August 2018
Mutation in fibrillin-1 and the Marfanoid-craniosynostosis (Shprintzen-Goldberg) 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=1717479
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15 August 2018
Altered cell differentiation and proliferation in mice lacking p57KIP2 indicates a role in Beckwith–Wiedemann 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=1717479
retrieved
1 December 2018
Glypicans: a growing trend
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=1717479
retrieved
1 December 2018
Parental imprinting of human chromosome region 11p15.3-pter involved in the Beckwith-Wiedemann syndrome and various human neoplasia
1 reference
stated in
PubMed
reference URL
https://pubmed.ncbi.nlm.nih.gov/9613346
retrieved
12 December 2020
based on heuristic
inferred from PubMed ID database lookup
Adrenocorticotropin receptor gene mutations in familial glucocorticoid deficiency: relationships with clinical features in four families
1 reference
stated in
PubMed
reference URL
https://pubmed.ncbi.nlm.nih.gov/9613346
retrieved
12 December 2020
based on heuristic
inferred from PubMed ID database lookup
Craniofacial syndromes: no such thing as a single gene disease
1 reference
stated in
PubMed
reference URL
https://pubmed.ncbi.nlm.nih.gov/9613346
retrieved
12 December 2020
based on heuristic
inferred from PubMed ID database lookup
Sotos syndrome
1 reference
stated in
PubMed
reference URL
https://pubmed.ncbi.nlm.nih.gov/9613346
retrieved
12 December 2020
based on heuristic
inferred from PubMed ID database lookup
Genetic imprinting in clinical genetics
1 reference
stated in
PubMed
reference URL
https://pubmed.ncbi.nlm.nih.gov/9613346
retrieved
12 December 2020
based on heuristic
inferred from PubMed ID database lookup
Genomic imprinting and gene activation in cancer
1 reference
stated in
PubMed
reference URL
https://pubmed.ncbi.nlm.nih.gov/9613346
retrieved
12 December 2020
based on heuristic
inferred from PubMed ID database lookup
One gene—four syndromes
1 reference
stated in
PubMed
reference URL
https://pubmed.ncbi.nlm.nih.gov/9613346
retrieved
12 December 2020
based on heuristic
inferred from PubMed ID database lookup
Identifiers
DOI
10.1136/ADC.78.3.200
1 reference
stated in
Europe PubMed Central
PMCID
1717479
retrieved
13 November 2017
PMCID
1717479
1 reference
stated in
Europe PubMed Central
PMCID
1717479
retrieved
13 November 2017
PubMed ID
9613346
1 reference
stated in
Europe PubMed Central
PMCID
1717479
retrieved
13 November 2017
ResearchGate publication ID
13671702
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