(Q48691452)

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Hereditary myopathy, oligophrenia, cataract, skeletal abnormalities and hypergonadotropic hypogonadism; a new syndrome

scientific article published in January 1973

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Europe PubMed Central

PubMed publication ID

4789103

retrieved

14 February 2018

reference URL

http://europepmc.org/abstract/MED/4789103

title

Hereditary myopathy, oligophrenia, cataract, skeletal abnormalities and hypergonadotropic hypogonadism; a new syndrome (English)

1 reference

stated in

Europe PubMed Central

PubMed publication ID

4789103

retrieved

14 February 2018

reference URL

http://europepmc.org/abstract/MED/4789103

1 reference

Lundberg PO

1

1 reference

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Europe PubMed Central

PubMed publication ID

4789103

retrieved

14 February 2018

reference URL

http://europepmc.org/abstract/MED/4789103

publication date

1 January 1973

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stated in

Europe PubMed Central

PubMed publication ID

4789103

retrieved

14 February 2018

reference URL

http://europepmc.org/abstract/MED/4789103

published in

European Neurology

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stated in

Europe PubMed Central

PubMed publication ID

4789103

retrieved

14 February 2018

reference URL

http://europepmc.org/abstract/MED/4789103

volume

10

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Europe PubMed Central

PubMed publication ID

4789103

retrieved

14 February 2018

reference URL

http://europepmc.org/abstract/MED/4789103

issue

5

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Europe PubMed Central

PubMed publication ID

4789103

retrieved

14 February 2018

reference URL

http://europepmc.org/abstract/MED/4789103

page(s)

261-280

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stated in

Europe PubMed Central

PubMed publication ID

4789103

retrieved

14 February 2018

reference URL

http://europepmc.org/abstract/MED/4789103

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DOI

10.1159/000114282

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PubMed publication ID

4789103

1 reference

stated in

Europe PubMed Central

PubMed publication ID

4789103

retrieved

14 February 2018

reference URL

http://europepmc.org/abstract/MED/4789103

(Q48691452)

Hereditary myopathy, oligophrenia, cataract, skeletal abnormalities and hypergonadotropic hypogonadism; a new syndrome

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