Literature DB >> 14462269

[On a rare association of craniofacial malformative syndrome and congenital absence of the fibula].

M LANZIERI.   

Abstract

Entities:  

Keywords:  FIBULA/abnormalities; SKULL/abnormalities

Mesh:

Year:  1961        PMID: 14462269

Source DB:  PubMed          Journal:  Ann Ottalmol Clin Ocul        ISSN: 0003-4665


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  1 in total

1.  Diaphragmatic hernia in a female newborn with focal dermal hypoplasia and marked asymmetric malformations (Goltz-Gorlin syndrome).

Authors:  J Kunze; K Heyne; H R Wiedemann
Journal:  Eur J Pediatr       Date:  1979-06-28       Impact factor: 3.183

  1 in total

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