(Q48822376)

English

High-resolution deletion mapping of chromosome arm 17p in childhood primitive neuroectodermal tumors reveals a common chromosomal disruption within the Smith-Magenis region, an unstable region in chromosome band 17p11.2.

scientific article published in January 1997

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scholarly article

1 reference

Europe PubMed Central

PubMed publication ID

15 February 2018

http://europepmc.org/abstract/MED/8993980

High-resolution deletion mapping of chromosome arm 17p in childhood primitive neuroectodermal tumors reveals a common chromosomal disruption within the Smith-Magenis region, an unstable region in chromosome band 17p11.2. (English)

1 reference

Europe PubMed Central

PubMed publication ID

15 February 2018

http://europepmc.org/abstract/MED/8993980

author name string

Scheurlen WG

1

1 reference

Europe PubMed Central

PubMed publication ID

15 February 2018

http://europepmc.org/abstract/MED/8993980

Seranski P

2

1 reference

Europe PubMed Central

PubMed publication ID

15 February 2018

http://europepmc.org/abstract/MED/8993980

Mincheva A

3

1 reference

Europe PubMed Central

PubMed publication ID

15 February 2018

http://europepmc.org/abstract/MED/8993980

Kühl J

4

1 reference

Europe PubMed Central

PubMed publication ID

15 February 2018

http://europepmc.org/abstract/MED/8993980

Sörensen N

5

1 reference

Europe PubMed Central

PubMed publication ID

15 February 2018

http://europepmc.org/abstract/MED/8993980

Krauss J

6

1 reference

Europe PubMed Central

PubMed publication ID

15 February 2018

http://europepmc.org/abstract/MED/8993980

Lichter P

7

1 reference

Europe PubMed Central

PubMed publication ID

15 February 2018

http://europepmc.org/abstract/MED/8993980

Poustka A

8

1 reference

Europe PubMed Central

PubMed publication ID

15 February 2018

http://europepmc.org/abstract/MED/8993980

Wilgenbus KK

9

1 reference

Europe PubMed Central

PubMed publication ID

15 February 2018

http://europepmc.org/abstract/MED/8993980

publication date

1 January 1997

1 reference

Europe PubMed Central

PubMed publication ID

15 February 2018

http://europepmc.org/abstract/MED/8993980

Genes, Chromosomes and Cancer

1 reference

Europe PubMed Central

PubMed publication ID

15 February 2018

http://europepmc.org/abstract/MED/8993980

18

1 reference

Europe PubMed Central

PubMed publication ID

15 February 2018

http://europepmc.org/abstract/MED/8993980

1

1 reference

Europe PubMed Central

PubMed publication ID

15 February 2018

http://europepmc.org/abstract/MED/8993980

50-58

1 reference

Europe PubMed Central

PubMed publication ID

15 February 2018

http://europepmc.org/abstract/MED/8993980

Interphase cytogenetics: a new tool for the study of genetic changes in brain tumors

1 reference

https://api.crossref.org/works/10.1002%2F%28SICI%291098-2264%28199701%2918%3A1%3C50%3A%3AAID-GCC6%3E3.0.CO%3B2-0

21 January 2018

Structural chromosomal abnormalities in human medulloblastoma

1 reference

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21 January 2018

Two patients with duplication of 17p11.2: the reciprocal of the Smith-Magenis syndrome deletion?

1 reference

https://api.crossref.org/works/10.1002%2F%28SICI%291098-2264%28199701%2918%3A1%3C50%3A%3AAID-GCC6%3E3.0.CO%3B2-0

21 January 2018

The 1993-94 Généthon human genetic linkage map

1 reference

https://api.crossref.org/works/10.1002%2F%28SICI%291098-2264%28199701%2918%3A1%3C50%3A%3AAID-GCC6%3E3.0.CO%3B2-0

21 January 2018

In vitro karyotypic and immunophenotypic characterisation of primitive neuroectodermal tumours: similarities to malignant gliomas

1 reference

https://api.crossref.org/works/10.1002%2F%28SICI%291098-2264%28199701%2918%3A1%3C50%3A%3AAID-GCC6%3E3.0.CO%3B2-0

21 January 2018

Cytogenetic analysis of 39 pediatric central nervous system tumors

1 reference

https://api.crossref.org/works/10.1002%2F%28SICI%291098-2264%28199701%2918%3A1%3C50%3A%3AAID-GCC6%3E3.0.CO%3B2-0

21 January 2018

Deregulated expression of PAX5 in medulloblastoma

1 reference

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21 January 2018

High-resolution mapping of human chromosome 11 by in situ hybridization with cosmid clones

1 reference

https://api.crossref.org/works/10.1002%2F%28SICI%291098-2264%28199701%2918%3A1%3C50%3A%3AAID-GCC6%3E3.0.CO%3B2-0

21 January 2018

Physical mapping of chromosome 17p13.3 in the region of a putative tumor suppressor gene important in medulloblastoma

1 reference

https://api.crossref.org/works/10.1002%2F%28SICI%291098-2264%28199701%2918%3A1%3C50%3A%3AAID-GCC6%3E3.0.CO%3B2-0

21 January 2018

A simple salting out procedure for extracting DNA from human nucleated cells

1 reference

https://api.crossref.org/works/10.1002%2F%28SICI%291098-2264%28199701%2918%3A1%3C50%3A%3AAID-GCC6%3E3.0.CO%3B2-0

21 January 2018

Parameters of the human genome

1 reference

https://api.crossref.org/works/10.1002%2F%28SICI%291098-2264%28199701%2918%3A1%3C50%3A%3AAID-GCC6%3E3.0.CO%3B2-0

21 January 2018

Cytogenetic analysis of 109 pediatric central nervous system tumors.

1 reference

https://api.crossref.org/works/10.1002%2F%28SICI%291098-2264%28199701%2918%3A1%3C50%3A%3AAID-GCC6%3E3.0.CO%3B2-0

21 January 2018

Revision of the World Health Organization classification of brain tumors for childhood brain tumors

1 reference

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21 January 2018

Medulloblastoma: II. A pathobiologic overview

1 reference

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21 January 2018

Cytogenetic studies in 45 pediatric brain tumors

1 reference

https://api.crossref.org/works/10.1002%2F%28SICI%291098-2264%28199701%2918%3A1%3C50%3A%3AAID-GCC6%3E3.0.CO%3B2-0

21 January 2018

Ordering of 66 STSs along the entire short arm of human chromosome 17 and chromosome assignment of a transcribed sequence (FMR1L2) homologous to FMR1.

1 reference

https://api.crossref.org/works/10.1002%2F%28SICI%291098-2264%28199701%2918%3A1%3C50%3A%3AAID-GCC6%3E3.0.CO%3B2-0

21 January 2018

Identifiers

10.1002/(SICI)1098-2264(199701)18:1<50::AID-GCC6>3.0.CO;2-0

1 reference

Europe PubMed Central

PubMed publication ID

15 February 2018

http://europepmc.org/abstract/MED/8993980

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

15 February 2018

http://europepmc.org/abstract/MED/8993980

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