Literature DB >> 7163273

Hanhart syndrome: possibility of autosomal recessive inheritance.

H Dellagrammaticas, M Tzaki, A Kapiki, L Sianidou, P Philippidis, C Papas, C Bartsocas.   

Abstract

Entities:  

Mesh：

Year:  1982        PMID： 7163273

Source DB:  PubMed          Journal:  Prog Clin Biol Res        ISSN： 0361-7742


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  2 in total

1.  Hypoglossia-hypodactyly syndrome with hydrocephalus: a clue to the aetiology?

Authors:  Y Gillerot; L Van Maldergem; R Chef; L Koulischer
Journal:  J Med Genet       Date:  1991-07       Impact factor: 6.318

2.  Hypoglossia-hypodactyly syndrome with short stature - a case report.

Authors:  Manisha Goyal; Ankur Singh; Pratiksha Singh; Seema Kapoor
Journal:  J Clin Diagn Res       Date:  2014-04-15
  2 in total

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