(Q53652241)

English

Mapping autosomal dominant progressive limb-girdle myopathy with bone fragility to chromosome 9p21-p22: a novel locus for a musculoskeletal syndrome.

scientific article published on 22 October 2005

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Europe PubMed Central

PubMed publication ID

16 May 2018

http://europepmc.org/abstract/MED/16244874

Mapping autosomal dominant progressive limb-girdle myopathy with bone fragility to chromosome 9p21-p22: a novel locus for a musculoskeletal syndrome. (English)

1 reference

Europe PubMed Central

PubMed publication ID

16 May 2018

http://europepmc.org/abstract/MED/16244874

Deborah V Novack

6

1 reference

Europe PubMed Central

PubMed publication ID

16 May 2018

http://europepmc.org/abstract/MED/16244874

Michael P. Whyte

8

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Michael P Whyte

1 reference

Europe PubMed Central

PubMed publication ID

16 May 2018

http://europepmc.org/abstract/MED/16244874

7

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Steven Mumm

1 reference

Europe PubMed Central

PubMed publication ID

16 May 2018

http://europepmc.org/abstract/MED/16244874

Virginia Kimonis

10

object named as

Virginia E Kimonis

1 reference

Europe PubMed Central

PubMed publication ID

16 May 2018

http://europepmc.org/abstract/MED/16244874

author name string

Giles D J Watts

1

1 reference

Europe PubMed Central

PubMed publication ID

16 May 2018

http://europepmc.org/abstract/MED/16244874

Sarju G Mehta

2

1 reference

Europe PubMed Central

PubMed publication ID

16 May 2018

http://europepmc.org/abstract/MED/16244874

Chengfeng Zhao

3

1 reference

Europe PubMed Central

PubMed publication ID

16 May 2018

http://europepmc.org/abstract/MED/16244874

Sheena Ramdeen

4

1 reference

Europe PubMed Central

PubMed publication ID

16 May 2018

http://europepmc.org/abstract/MED/16244874

Sara Jane Hamilton

5

1 reference

Europe PubMed Central

PubMed publication ID

16 May 2018

http://europepmc.org/abstract/MED/16244874

Barbara Mc Gillivray

9

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Europe PubMed Central

PubMed publication ID

16 May 2018

http://europepmc.org/abstract/MED/16244874

publication date

22 October 2005

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Europe PubMed Central

PubMed publication ID

16 May 2018

http://europepmc.org/abstract/MED/16244874

1 reference

Europe PubMed Central

PubMed publication ID

16 May 2018

http://europepmc.org/abstract/MED/16244874

118

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Europe PubMed Central

PubMed publication ID

16 May 2018

http://europepmc.org/abstract/MED/16244874

3-4

1 reference

Europe PubMed Central

PubMed publication ID

16 May 2018

http://europepmc.org/abstract/MED/16244874

508-514

1 reference

Europe PubMed Central

PubMed publication ID

16 May 2018

http://europepmc.org/abstract/MED/16244874

Hereditary bone dysplasia with sarcomatous degeneration. Study of a family.

1 reference

https://api.crossref.org/works/10.1007%2FS00439-005-0075-Z

21 January 2018

Localization of the 9p Melanoma Susceptibility Locus (MLM) to a 2-cM Region between D9S736 and D9S171

1 reference

https://pubmed.ncbi.nlm.nih.gov/16244874

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Mutations in a member of the ADAMTS gene family cause thrombotic thrombocytopenic purpura

1 reference

https://pubmed.ncbi.nlm.nih.gov/16244874

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

ADAMTS: a novel family of extracellular matrix proteases

1 reference

https://pubmed.ncbi.nlm.nih.gov/16244874

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Diaphyseal medullary stenosis with malignant fibrous histiocytoma: a hereditary bone dysplasia/cancer syndrome maps to 9p21-22

1 reference

https://pubmed.ncbi.nlm.nih.gov/16244874

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The UCSC Genome Browser Database

1 reference

https://pubmed.ncbi.nlm.nih.gov/16244874

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Inclusion body myopathy associated with Paget disease of bone and frontotemporal dementia is caused by mutant valosin-containing protein

1 reference

https://pubmed.ncbi.nlm.nih.gov/16244874

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Faster sequential genetic linkage computations

1 reference

https://pubmed.ncbi.nlm.nih.gov/16244874

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Genomic cloning of methylthioadenosine phosphorylase: a purine metabolic enzyme deficient in multiple different cancers

1 reference

https://pubmed.ncbi.nlm.nih.gov/16244874

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Hereditary bone dysplasia with malignant change. Report of three families.

1 reference

https://pubmed.ncbi.nlm.nih.gov/16244874

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Abnormality of the long bones and progressive muscular dystrophy in a family

1 reference

https://pubmed.ncbi.nlm.nih.gov/16244874

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Genes on chromosomes 4, 9, and 19 involved in 11q23 abnormalities in acute leukemia share sequence homology and/or common motifs

1 reference

https://pubmed.ncbi.nlm.nih.gov/16244874

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Cloning of a novel family of mammalian GTP-binding proteins (RagA, RagBs, RagB1) with remote similarity to the Ras-related GTPases

1 reference

https://pubmed.ncbi.nlm.nih.gov/16244874

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The gene for multiple familial trichoepithelioma maps to chromosome 9p21.

1 reference

https://pubmed.ncbi.nlm.nih.gov/16244874

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Manifestations in a family with autosomal dominant bone fragility and limb-girdle myopathy.

1 reference

https://pubmed.ncbi.nlm.nih.gov/16244874

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Structure of the gene encoding mouse adipose differentiation-related protein (ADRP).

1 reference

https://pubmed.ncbi.nlm.nih.gov/16244874

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The human homolog of the mouse brown gene maps to the short arm of chromosome 9 and extends the known region of homology with mouse chromosome 4

1 reference

https://pubmed.ncbi.nlm.nih.gov/16244874

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Punctin, a novel ADAMTS-like molecule, ADAMTSL-1, in extracellular matrix

1 reference

https://pubmed.ncbi.nlm.nih.gov/16244874

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Malignant fibrous histiocytoma: inherited and sporadic forms have loss of heterozygosity at chromosome bands 9p21-22-evidence for a common genetic defect.

1 reference

https://pubmed.ncbi.nlm.nih.gov/16244874

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Mapping of the shortest region of overlap of deletions of the short arm of chromosome 9 associated with human neoplasia

1 reference

https://pubmed.ncbi.nlm.nih.gov/16244874

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1007/S00439-005-0075-Z

1 reference

Europe PubMed Central

PubMed publication ID

16 May 2018

http://europepmc.org/abstract/MED/16244874

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

16 May 2018

http://europepmc.org/abstract/MED/16244874

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