(Q33680230)

28 July 2017

title

A patient with Simpson-Golabi-Behmel syndrome and hepatocellular carcinoma (English)

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Simpson-Golabi-Behmel syndrome

28 July 2017

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1 reference

inferred from title

hepatocellular carcinoma

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8

Hughes-Benzie R

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28 July 2017

Lapunzina P

1

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28 July 2017

Badia I

2

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28 July 2017

Galoppo C

3

1 reference

28 July 2017

De Matteo E

4

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28 July 2017

Silberman P

5

1 reference

28 July 2017

Tello A

6

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28 July 2017

Grichener J

7

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28 July 2017

language of work or name

English

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publication date

1 February 1998

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Journal of Medical Genetics

28 July 2017

published in

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28 July 2017

volume

35

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28 July 2017

issue

2

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28 July 2017

page(s)

153-156

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Large scale deletions in the GPC3 gene may account for a minority of cases of Simpson-Golabi-Behmel syndrome.

28 July 2017

cites work

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1051222

Mutations in GPC3, a glypican gene, cause the Simpson-Golabi-Behmel overgrowth syndrome

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1051222

Mapping of Simpson-Golabi-Behmel syndrome to Xq25-q27

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1051222

Frequent loss of heterozygosity on 6q at the mannose 6-phosphate/insulin-like growth factor II receptor locus in human hepatocellular tumors

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1051222

M6P/IGF2R gene is mutated in human hepatocellular carcinomas with loss of heterozygosity

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1051222

A new X-linked mental retardation-overgrowth syndrome.

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1051222

Simpson-Golabi-Behmel syndrome associated with renal dysplasia and embryonal tumor: localization of the gene to Xqcen-q21.

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1051222

The importance of differentiating Simpson-Golabi-Behmel and Beckwith-Wiedemann syndromes

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1051222

Report of another family with Simpson-Golabi-Behmel syndrome and a review of the literature

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1051222

A case study of Beckwith-Wiedemann syndrome associated with hepatoblastoma.

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1051222

Glypicans: a growing trend

30 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1051222

Gene for Simpson-Golabi-Behmel syndrome is linked to HPRT in Xq26 in two European families

30 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1051222

Simpson-Golabi-Behmel syndrome (SGBS) in a female with an X-autosome translocation

30 October 2018

1 reference

12 December 2020

Simpson-Golabi-Behmel syndrome: disproportionate fetal overgrowth and elevated maternal serum alpha-fetoprotein

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12 December 2020

Infantile lethal variant of Simpson-Golabi-Behmel syndrome associated with hydrops fetalis

1 reference

12 December 2020

Simpson-Golabi-Behmel syndrome: genotype/phenotype analysis of 18 affected males from 7 unrelated families

1 reference

12 December 2020

Hepatoblastoma and hepatocarcinoma in infancy and childhood. Report of 47 cases

1 reference

12 December 2020

A previously unrecognized X-linked syndrome of dysmorphia

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12 December 2020

A new X-linked dysplasia gigantism syndrome: identical with the Simpson dysplasia syndrome?

1 reference

12 December 2020

Hepatocellular carcinoma associated with congenital macronodular cirrhosis in a neonate

1 reference

12 December 2020

Simpson-Golabi-Behmel syndrome: follow-up of the Michigan family

1 reference

12 December 2020

Opsoclonus-myoclonus with Beckwith-Wiedemann syndrome and hepatoblastoma

1 reference

12 December 2020

Identifiers

DOI

10.1136/JMG.35.2.153

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28 July 2017

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28 July 2017

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