(Q34315394)

1 August 2017

Assignment of the developmentally regulated gene NEDD1 to human chromosome 12q22 by fluorescence in situ hybridization (English)

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1 August 2017

Takai S

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1 August 2017

Yoshida Y

2

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1 August 2017

Noda M

3

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1 August 2017

Yamada K

4

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1 August 2017

Kumar S

5

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1 August 2017

1 January 1995

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1 August 2017

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1 August 2017

95

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1 August 2017

96-98

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1 August 2017

1

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describes a project that uses

1 August 2017

fluorescence in situ hybridization

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https://scigraph.springernature.com/pub.10.1007/bf00225082

inferred from title

exact match

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cites work

Human high-affinity Fc gamma RI (CD64) gene mapped to chromosome 1q21.2-q21.3 by fluorescence in situ hybridization

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12 December 2020

Identification of a set of genes with developmentally down-regulated expression in the mouse brain

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12 December 2020

Mapping of the KREV1 transformation suppressor gene and its pseudogene (KREV1P) to human chromosome 1p13.3 and 14q24.3, respectively, by fluorescence in situ hybridization

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12 December 2020

Mapping of the MYC gene to band 8q24.12----q24.13 by R-banding and distal to fra(8)(q24.11), FRA8E, by fluorescence in situ hybridization

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12 December 2020

Molecular cloning and biological activity of a novel developmentally regulated gene encoding a protein with beta-transducin-like structure

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12 December 2020

Cytogenetic analysis using quantitative, high-sensitivity, fluorescence hybridization

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12 December 2020

A gene for Holt–Oram syndrome maps to the distal long arm of chromosome 12

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12 December 2020

Sensitive, high-resolution chromatin and chromosome mapping in situ: presence and orientation of two closely integrated copies of EBV in a lymphoma line

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12 December 2020

Mapping of the human gene encoding the mutual signal-transducing subunit (beta-chain) of granulocyte-macrophage colony-stimulating factor (GM-CSF), interleukin-3 (IL-3), and interleukin-5 (IL-5) receptor complexes to chromosome 22q13.1.

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12 December 2020

Cytogenetic and molecular analysis of human male germ cell tumors: chromosome 12 abnormalities and gene amplification

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12 December 2020

Holt-Oram syndrome is a genetically heterogeneous disease with one locus mapping to human chromosome 12q

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12 December 2020

R-banding and nonisotopic in situ hybridization: precise localization of the human type II collagen gene (COL2A1)

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12 December 2020

Identifiers

DOI

10.1007/BF00225082

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Dimensions Publication ID

1 August 2017

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