Literature DB >> 6078173

[The frequency and mutation-rate of the Apert syndrome].

W Tünte, W Lenz.   

Abstract

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Year:  1967        PMID: 6078173     DOI: 10.1007/bf00291254

Source DB:  PubMed          Journal:  Humangenetik        ISSN: 0018-7348


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  12 in total

1.  ACROCEPHALOSYNDACTYLY IN SINGAPORE. A STUDY OF FIVE CHINESE MALES.

Authors:  V K PILLAY
Journal:  J Bone Joint Surg Br       Date:  1964-02

2.  [OSTEOGENESIS IMPERFECTA. A CLINICAL-HEREDITARY-BIOLOGICAL STUDY ON PATIENTS IN WESTPHALIA. CALCULATION OF THE MUTATION RATE FOR THE ADMINISTRATIVE AREA OF MUENSTER (WESTPHALIA)].

Authors:  G SCHROEDER
Journal:  Z Mensch Vererb Konstitutionsl       Date:  1964-08-25

3.  [DOMINANT HEREDITARY ACROCEPHALOSYNDACTYLIA].

Authors:  R A PFEIFFER
Journal:  Z Kinderheilkd       Date:  1964-09-16

4.  [Mechanism of some spontaneous mutations in man].

Authors:  F VOGEL
Journal:  Z Mensch Vererb Konstitutionsl       Date:  1958

5.  Achondroplasia: an account of the condition in Northern Ireland.

Authors:  A C STEVENSON
Journal:  Am J Hum Genet       Date:  1957-03       Impact factor: 11.025

6.  [New studies on the genetics of retinoblastoma; glioma retinae].

Authors:  F VOGEL
Journal:  Z Mensch Vererb Konstitutionsl       Date:  1957

7.  Marfan's syndrome in Northern Ireland; an account of thirteen families.

Authors:  M A LYNAS
Journal:  Ann Hum Genet       Date:  1958-07       Impact factor: 1.670

8.  Congenital Aniridia.

Authors:  M W Shaw; H F Falls; J V Neel
Journal:  Am J Hum Genet       Date:  1960-12       Impact factor: 11.025

9.  [The development of hemophilia A through mutations in male germ cells].

Authors:  J Herrmann; G Landbeck; W Lenz
Journal:  Dtsch Med Wochenschr       Date:  1966-12-23       Impact factor: 0.628

10.  Apert's syndrome (a type of acrocephalosyndactyly)-observations on a British series of thirty-nine cases.

Authors:  C E BLANK
Journal:  Ann Hum Genet       Date:  1960-05       Impact factor: 1.670

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