Gershoni-Baruch syndrome: Report of a new family confirming autosomal recessive inheritance

American Journal of Medical Genetics

Volumn 122 A, Issue 2, 2003, Pages 174-179

  Franceschini, P ^a,e   Guala, A ^b   Licata, D ^a   Botta, G ^c   Flora, F ^d   Angeli, G ^d   Di Cara, G ^a   Franceschini, D ^a  

^a UNIVERSITY OF TURIN   (Italy)

^b Ospedale SS Pietro e Paolo   (Italy)

^c ASO OIRM Sant'Anna   (Italy)

^d SANT'ANDREA HOSPITAL   (Italy)

^e Servizio di Genetica Clinica   (Italy)

Author keywords

Autosomal recessive; Cadiovascular abnormalities; Diphragmatic hernia; Gershoni Baruch syndrome; Omphalocele; Radial ray defects

Indexed keywords

ARTICLE; AUTOSOMAL RECESSIVE INHERITANCE; BONE DEFECT; CARDIOVASCULAR DISEASE; CASE REPORT; CONGENITAL MALFORMATION; DIAPHRAGM HERNIA; FAMILIAL DISEASE; FEMALE; FETUS; GERSHONI BARUCH SYNDROME; HUMAN; LIMB MALFORMATION; MULTIGENE FAMILY; OMPHALOCELE; PREGNANCY TERMINATION; PRIORITY JOURNAL;

RAPHIA FRATER;

EID: 0141568817     PISSN: 15524825     EISSN: None     Source Type: Journal    
DOI: 10.1002/ajmg.a.20275     Document Type: Article

References (9)

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