(Q28303036)

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Mapping of the Simpson-Golabi-Behmel overgrowth syndrome gene (GPC3) to chromosome X in human and rat by fluorescence in situ hybridization

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Mapping of the Simpson-Golabi-Behmel overgrowth syndrome gene (GPC3) to chromosome X in human and rat by fluorescence in situ hybridization (English)

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T Shen

1

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G Sonoda

series ordinal

2

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J Hamid

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3

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M Li

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4

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J Filmus

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5

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R N Buick

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6

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J R Testa

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7

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language of work or name

English

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publication date

January 1997

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published in

Mammalian Genome

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volume

8

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issue

1

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page(s)

72

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describes a project that uses

fluorescence in situ hybridization

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cites work

Isolation of a cDNA corresponding to a developmentally regulated transcript in rat intestine

1 reference

stated in

Crossref

reference URL

https://api.crossref.org/works/10.1007%2FS003359900357

retrieved

21 January 2018

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

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stated in

Crossref

reference URL

https://api.crossref.org/works/10.1007%2FS003359900357

retrieved

21 January 2018

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

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stated in

Crossref

reference URL

https://api.crossref.org/works/10.1007%2FS003359900357

retrieved

21 January 2018

Localization of the interferon-alpha gene cluster to rat chromosome bands 5q31----q33 by fluorescence in situ hybridization

1 reference

stated in

Crossref

reference URL

https://api.crossref.org/works/10.1007%2FS003359900357

retrieved

21 January 2018

Integral membrane heparan sulfate proteoglycans

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stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/9021160

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12 December 2020

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DOI

10.1007/S003359900357

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PubMed publication ID

9021160

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(Q28303036)

Mapping of the Simpson-Golabi-Behmel overgrowth syndrome gene (GPC3) to chromosome X in human and rat by fluorescence in situ hybridization

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