Chromosomal and clinical features in an infant with Hallermann-Streiff syndrome [3]

Archives of Disease in Childhood

Volumn 77, Issue 2, 1997, Pages 184-

  Pugliese, G F ^a   Latorre, G ^a   Latorre, F ^a  

^a Ospedale Regionale 'Di Venere'   (Italy)

Author keywords

[No Author keywords available]

Indexed keywords

CASE REPORT; CHROMOSOME ABERRATION; CLINICAL FEATURE; FEMALE; GENETIC POLYMORPHISM; HALLERMANN STREIFF SYNDROME; HUMAN; LETTER; MULTIPLE MALFORMATION SYNDROME; NEWBORN; PRIORITY JOURNAL;

FEMALE; HALLERMANN'S SYNDROME; HUMANS; INFANT, NEWBORN; POLYMORPHISM, GENETIC; RADIUS FRACTURES;

EID: 0030885136     PISSN: 00039888     EISSN: 14682044     Source Type: Journal    
DOI: None     Document Type: Letter

References (4)