(Q42489729)

1 November 2017

Report and abstracts of the Third International Workshop on Chromosome 9. Cambridge, United Kingdom, 9-11 April, 1994. (English)

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1 November 2017

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4

J L Haines

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1 November 2017

S Povey

1

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1 November 2017

J Armour

2

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1 November 2017

P Farndon

3

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1 November 2017

M Knowles

5

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1 November 2017

F Olopade

6

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1 November 2017

A Pilz

7

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1 November 2017

J A White

8

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D J Kwiatkowski

9

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1 November 2017

language of work or name

English

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publication date

1 July 1994

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1 November 2017

Annals of Human Genetics

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1 November 2017

58

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1 November 2017

177-250

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1 November 2017

Pt 3

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Identification of human chromosome 9 specific genes using exon amplification

1 November 2017

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https://api.crossref.org/works/10.1111%2FJ.1469-1809.1994.TB01887.X

Structure, function, and chromosome mapping of the growth-suppressing human homologue of the murine gas1 gene

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1469-1809.1994.TB01887.X

Localization of the human growth arrest-specific gene (GAS1) to chromosome bands 9q21.3-q22, a region frequently deleted in myeloid malignancies

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1469-1809.1994.TB01887.X

A cell cycle regulator potentially involved in genesis of many tumor types

21 January 2018

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https://api.crossref.org/works/10.1111%2FJ.1469-1809.1994.TB01887.X

Human very-low-density lipoprotein receptor complementary DNA and deduced amino acid sequence and localization of its gene (VLDLR) to chromosome band 9p24 by fluorescence in situ hybridization

21 January 2018

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https://api.crossref.org/works/10.1111%2FJ.1469-1809.1994.TB01887.X

Deletions of the cyclin-dependent kinase-4 inhibitor gene in multiple human cancers

21 January 2018

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https://api.crossref.org/works/10.1111%2FJ.1469-1809.1994.TB01887.X

Assignment of the gene coding for the human high-affinity glutamate transporter EAAC1 to 9p24: potential role in dicarboxylic aminoaciduria and neurodegenerative disorders

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1469-1809.1994.TB01887.X

High-resolution genetic mapping of the cartilage-hair hypoplasia (CHH) gene in Amish and Finnish families.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1469-1809.1994.TB01887.X

Gene mapping in a murine cell line by immunoselection with cytotoxic T lymphocytes

21 January 2018

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https://api.crossref.org/works/10.1111%2FJ.1469-1809.1994.TB01887.X

Localization of a gene for Fukuyama type congenital muscular dystrophy to chromosome 9q31-33

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1469-1809.1994.TB01887.X

The MLLT3 gene maps between D9S156 and D9S171 and contains an unstable polymorphic trinucleotide repeat.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1469-1809.1994.TB01887.X

A common mutation in the FACC gene causes Fanconi anaemia in Ashkenazi Jews

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1469-1809.1994.TB01887.X

CEPH Consortium Map of Chromosome 9

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1469-1809.1994.TB01887.X

10.1111/J.1469-1809.1994.TB01887.X

21 January 2018

Identifiers

DOI

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1 November 2017

1 reference