Literature DB >> 20269277

[Not Available].

A FRANCESCHETTI, D KLEIN.   

Abstract

Keywords:  ATAXIA/friedreich type; RETINITIS/pigmentosa, genetics; RETINITIS/punctata albescena, heredity; TAPETORETINAL DEGENERATION/friedreich ataxia

Mesh：

Year:  1947        PMID： 20269277

Source DB:  PubMed          Journal:  Arch Julius Klaus Stift Vererbungsforsch Sozialanthropol Rassenhyg        ISSN： 0003-8881


× No keyword cloud information.
  2 in total

1.  [Retinitis pigmentosa, symmetrical inner ear deafness, typical inverse vascular fistula symptom without fistula and vestibular sensitivity disease; combined hereditary ear and eye diseases].

Authors:  H H STENGER
Journal:  Arch Ohren Nasen Kehlkopfheilkd       Date:  1956

2.  [Genetic relations between myatrophies and psychoses].

Authors:  K H PARNITZKE; R SEIDEL
Journal:  Dtsch Z Nervenheilkd       Date:  1961
  2 in total

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