Normal dosage of the insulin and insulin-like growth factor II genes in patients with the Beckwith-Wiedemann syndrome. (Q35198658)

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28 September 2019

title

Normal dosage of the insulin and insulin-like growth factor II genes in patients with the Beckwith-Wiedemann syndrome (English)

1 reference

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28 September 2019

1

Spritz RA

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28 September 2019

author name string

Mager D

series ordinal

2

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28 September 2019

Pauli RM

series ordinal

3

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28 September 2019

Laxova R

series ordinal

4

1 reference

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28 September 2019

language of work or name

English

0 references

publication date

1 August 1986

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American Journal of Human Genetics

28 September 2019

published in

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28 September 2019

volume

39

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28 September 2019

issue

2

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28 September 2019

page(s)

265-273

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FAMILIAL MALFORMATION COMPLEX WITH UMBILICAL HERNIA AND MACROGLOSSIA--A "NEW SYNDROME"?

28 September 2019

cites work

1 reference

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Localization of the human insulin gene to the distal end of the short arm of chromosome 11.

13 July 2018

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Direct gene dosage determination in patients with unbalanced chromosomal aberrations using cloned DNA sequences. Application to the regional assignment of the gene for alpha 2(I) procollagen (COLIA2).

13 July 2018

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Abnormality of chromosome 11 in patients with features of Beckwith-Wiedemann syndrome

13 July 2018

1 reference

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Insulin-like growth factor II precursor gene organization in relation to insulin gene family

13 July 2018

1 reference

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Isolation and regional localization of DNA segments revealing polymorphic loci from human chromosome 13

13 July 2018

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Variation in the sequence and modification state of the human insulin gene flanking regions

13 July 2018

1 reference

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Polymorphic DNA region adjacent to the 5' end of the human insulin gene

13 July 2018

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Genetic Variation in the Human Insulin Gene

13 July 2018

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Exomphalos with macroglossia: a study of eleven cases.

13 July 2018

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The Wiedemann-Beckwith syndrome: genetic considerations and a diagnostic sign.

13 July 2018

1 reference

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Isolation of the human insulin-like growth factor genes: insulin-like growth factor II and insulin genes are contiguous

13 July 2018

1 reference

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Insulin-like growth factor-II gene expression in Wilms' tumour and embryonic tissues.

13 July 2018

1 reference

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Linkage map of the short arm of human chromosome 11: location of the genes for catalase, calcitonin, and insulin-like growth factor II.

13 July 2018

1 reference

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Detection of specific sequences among DNA fragments separated by gel electrophoresis

13 July 2018

1 reference

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A general method for isolation of high molecular weight DNA from eukaryotes

13 July 2018

1 reference

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Studies of malformation syndromes of man XXIX: the Wiedemann-Beckwith syndrome. Clinical, genetic and pathogenetic studies of 12 cases

13 July 2018

1 reference

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Familial occurrence of the Wiedemann-Beckwith syndrome and persistent fontanel

13 July 2018

1 reference

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Aniridia-Wilms’ tumor association: evidence for specific deletion of 11p13

13 July 2018

1 reference

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Chromosomal imbalance in the Aniridia-Wilms' tumor association: 11p interstitial deletion

13 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1683936

Neoplasms associated with the Beckwith-Wiedemann syndrome

13 July 2018

1 reference

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Letter: Wiedemann-Beckwith syndrome

13 July 2018

1 reference

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The highly polymorphic region near the human insulin gene is composed of simple tandemly repeating sequences

13 July 2018

1 reference

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Trisomy 11p15 and Beckwith-Wiedemann syndrome. A report of two cases.

26 September 2018

1 reference

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Unexpected relationships between four large deletions in the human beta-globin gene cluster

26 September 2018

1 reference

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Somatic deletion and duplication of genes on chromosome 11 in Wilms' tumours.

26 September 2018

1 reference

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The c-Ha-ras1, insulin and β-globin loci map outside the deletion associated with aniridia-Wilms' tumour

26 September 2018

1 reference

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Wiedemann-Beckwith syndrome

26 September 2018

1 reference

12 December 2020

Letter: Autosomal-dominant sex-dependent transmission of the Wiedemann-Beckwith syndrome

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12 December 2020

Familial macroglossia-omphalocele syndrome

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12 December 2020

Beckwith-Wiedemann syndrome in a mother and her son

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12 December 2020

Complete and incomplete forms of Beckwith-Wiedemann syndrome: their oncogenic potential

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12 December 2020

Wiedemann and Beckwith syndrome: a new familial case

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12 December 2020

Wiedemann-Beckwith syndrome: autosomal-dominant inheritance in a family

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12 December 2020

A Polymorphic Locus Near the Human Insulin Gene Is Associated with Insulin-dependent Diabetes Melliitus

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12 December 2020

Chromosome 11 and Beckwith-Wiedemann syndrome

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12 December 2020

Loss of alleles at loci on human chromosome 11 during genesis of Wilms' tumour

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12 December 2020

Development of homozygosity for chromosome 11p markers in Wilms' tumour

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12 December 2020

Loss of a Harvey ras allele in sporadic Wilms' tumour

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12 December 2020

Loss of heterozygosity in three embryonal tumours suggests a common pathogenetic mechanism

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12 December 2020

Expression of insulin-like growth factor-II transcripts in Wilms' tumour

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12 December 2020

Letter: Pseudo-Beckwith-Wiedemann syndrome: interaction with maternal diabetes

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12 December 2020

Identifiers

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:3529947%20AND%20SRC:MED&resulttype=core&format=json

28 September 2019

PubMed publication ID

3529947

1 reference