(Q34532857)

English

MASA syndrome: further clinical delineation and chromosomal localisation

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scholarly article

1 reference

Europe PubMed Central

PubMed publication ID

2 August 2017

MASA syndrome: further clinical delineation and chromosomal localisation (English)

1 reference

Europe PubMed Central

PubMed publication ID

2 August 2017

1 reference

based on heuristic

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5

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Europe PubMed Central

PubMed publication ID

2 August 2017

author name string

Winter RM

1

1 reference

Europe PubMed Central

PubMed publication ID

2 August 2017

Davies KE

2

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Europe PubMed Central

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2 August 2017

Bell MV

3

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Europe PubMed Central

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2 August 2017

Huson SM

4

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Europe PubMed Central

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2 August 2017

publication date

1 July 1989

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Europe PubMed Central

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2 August 2017

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Europe PubMed Central

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2 August 2017

82

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Europe PubMed Central

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2 August 2017

4

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Europe PubMed Central

PubMed publication ID

2 August 2017

367-370

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Europe PubMed Central

PubMed publication ID

2 August 2017

Toward a complete linkage map of the human X chromosome: regional assignment of 16 cloned single-copy DNA sequences employing a panel of somatic cell hybrids

1 reference

https://pubmed.ncbi.nlm.nih.gov/2737668

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Etiological heterogeneity in X-linked spastic paraplegia

1 reference

https://pubmed.ncbi.nlm.nih.gov/2737668

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Linkage studies of X-linked recessive spastic paraplegia using DNA probes.

1 reference

https://pubmed.ncbi.nlm.nih.gov/2737668

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Mental retardation-clasped thumb syndrome.

1 reference

https://pubmed.ncbi.nlm.nih.gov/2737668

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The MASA syndrome: a new heritable mental retardation syndrome

1 reference

https://pubmed.ncbi.nlm.nih.gov/2737668

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Multilocus linkage analysis in humans: detection of linkage and estimation of recombination

1 reference

https://pubmed.ncbi.nlm.nih.gov/2737668

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

X-linked mental retardation associated with bilateral clasp thumb anomaly.

1 reference

https://pubmed.ncbi.nlm.nih.gov/2737668

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1007/BF00273999

1 reference

Europe PubMed Central

PubMed publication ID

2 August 2017

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PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

2 August 2017

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