Literature DB >> 492868

[The Mohr syndrome (orofaciodigital syndrome type II). 1 familial case].

J B Cotton, R Gardet, J P Ladreyt, P Guibaud.   

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Year:  1979        PMID： 492868

Source DB:  PubMed          Journal:  Pediatrie        ISSN： 0031-4021


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  1 in total

1.  An autosomal recessive disorder with retardation of growth, mental deficiency, ptosis, pectus excavatum and camptodactyly.

Authors:  F Khaldi; B Bennaceur; A Hammou; M Hamza; H A Gharbi
Journal:  Pediatr Radiol       Date:  1988
  1 in total

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