(Q34559291)

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Homozygotes for Huntington's disease

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Europe PubMed Central

PubMed publication ID

3 August 2017

Homozygotes for Huntington's disease (English)

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Europe PubMed Central

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3 August 2017

Huntington's disease

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author name string

Wexler NS

1

1 reference

Europe PubMed Central

PubMed publication ID

3 August 2017

Young AB

2

1 reference

Europe PubMed Central

PubMed publication ID

3 August 2017

Tanzi RE

3

1 reference

Europe PubMed Central

PubMed publication ID

3 August 2017

Travers H

4

1 reference

Europe PubMed Central

PubMed publication ID

3 August 2017

Starosta-Rubinstein S

5

1 reference

Europe PubMed Central

PubMed publication ID

3 August 2017

Penney JB

6

1 reference

Europe PubMed Central

PubMed publication ID

3 August 2017

Snodgrass SR

7

1 reference

Europe PubMed Central

PubMed publication ID

3 August 2017

Shoulson I

8

1 reference

Europe PubMed Central

PubMed publication ID

3 August 2017

Gomez F

9

1 reference

Europe PubMed Central

PubMed publication ID

3 August 2017

Ramos Arroyo MA

10

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3 August 2017

language of work or name

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publication date

1 March 1987

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Europe PubMed Central

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3 August 2017

number of pages

4

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PubMed publication ID

3 August 2017

326

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Europe PubMed Central

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3 August 2017

6109

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Europe PubMed Central

PubMed publication ID

3 August 2017

194-197

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Europe PubMed Central

PubMed publication ID

3 August 2017

Familial hypercholesterolemia. A genetic regulatory defect in cholesterol metabolism

1 reference

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Dominance and homozygosity in man

1 reference

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Dominance and recessivity in medical genetics

1 reference

https://api.crossref.org/works/10.1038%2F326194A0

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Dominance and homozygosity in man

1 reference

https://api.crossref.org/works/10.1038%2F326194A0

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A polymorphic DNA marker genetically linked to Huntington's disease

1 reference

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7 January 2021

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Deletion of Huntington's disease-linked G8 (D4S10) locus in Wolf-Hirschhorn syndrome.

1 reference

https://api.crossref.org/works/10.1038%2F326194A0

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DNA Markers for Nervous System Diseases

1 reference

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Huntington's disease in Venezuela: neurologic features and functional decline

1 reference

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Huntington disease: functional capacities in patients treated with neuroleptic and antidepressant drugs

1 reference

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“Mini-mental state”

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Conduct disorder and affective disorder among the offspring of patients with Huntington's Disease

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Psychiatric syndromes in Huntington's disease

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Homozygous achondroplasia with survival beyond infancy

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Homozygosity for autosomal dominant Marfan syndrome

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A probable case of the homozygous condition of the aniridia gene.

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Dominantly inherited macular degeneration (Best's disease) in a homozygous father with 11 children

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Molecular Genetics of the Bithorax Complex in Drosophila melanogaster.

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Huntington disease: Clinical care and evaluation

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Use of cyclosporin A in establishing Epstein-Barr virus-transformed human lymphoblastoid cell lines

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Precise localization of human beta-globin gene complex on chromosome 11

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Imagery, encoding, and retrieval of information from memory: Some specific encoding-retrieval changes in Huntington's disease

1 reference

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7 January 2021

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Identifiers

10.1038/326194A0

1 reference

Europe PubMed Central

PubMed publication ID

3 August 2017

Dimensions Publication ID

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PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

3 August 2017

ResearchGate publication ID

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