(Q52735663)

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The effect of a change in mutation rate on the incidence of dominant and X-linked recessive disorders in man.

scientific article published in August 1981

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Europe PubMed Central

PubMed publication ID

7196989

retrieved

6 May 2018

reference URL

http://europepmc.org/abstract/MED/7196989

title

The effect of a change in mutation rate on the incidence of dominant and X-linked recessive disorders in man. (English)

1 reference

stated in

Europe PubMed Central

PubMed publication ID

7196989

retrieved

6 May 2018

reference URL

http://europepmc.org/abstract/MED/7196989

author name string

Childs JD

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1

1 reference

stated in

Europe PubMed Central

PubMed publication ID

7196989

retrieved

6 May 2018

reference URL

http://europepmc.org/abstract/MED/7196989

language of work or name

English

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publication date

1 August 1981

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Europe PubMed Central

PubMed publication ID

7196989

retrieved

6 May 2018

reference URL

http://europepmc.org/abstract/MED/7196989

published in

Mutation Research

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Europe PubMed Central

PubMed publication ID

7196989

retrieved

6 May 2018

reference URL

http://europepmc.org/abstract/MED/7196989

volume

83

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Europe PubMed Central

PubMed publication ID

7196989

retrieved

6 May 2018

reference URL

http://europepmc.org/abstract/MED/7196989

issue

1

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Europe PubMed Central

PubMed publication ID

7196989

retrieved

6 May 2018

reference URL

http://europepmc.org/abstract/MED/7196989

page(s)

145-158

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Europe PubMed Central

PubMed publication ID

7196989

retrieved

6 May 2018

reference URL

http://europepmc.org/abstract/MED/7196989

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DOI

10.1016/0027-5107(81)90079-8

1 reference

stated in

Europe PubMed Central

PubMed publication ID

7196989

retrieved

6 May 2018

reference URL

http://europepmc.org/abstract/MED/7196989

PubMed publication ID

7196989

1 reference

stated in

Europe PubMed Central

PubMed publication ID

7196989

retrieved

6 May 2018

reference URL

http://europepmc.org/abstract/MED/7196989

(Q52735663)

The effect of a change in mutation rate on the incidence of dominant and X-linked recessive disorders in man.

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