Agnathia-holoprosencephaly-situs inversus [1]

American Journal of Medical Genetics

Volumn 91, Issue 3, 2000, Pages 235-236

  Özden, Selçuk ^a,b   Fiçiciolu, Cem ^a   Kara, Mustafa ^a   Oral, O ^a   Bilgiç, Remziye ^a  

^a Zeynep Kamil Women's and Children's Hospital   (Turkey)

^b Ethem Efendi Cad   (Turkey)

Author keywords

[No Author keywords available]

Indexed keywords

CASE REPORT; DISEASE ASSOCIATION; GENE EXPRESSION; GENE MUTATION; HOLOPROSENCEPHALY; HUMAN; INFANT; LETTER; LYMPHOCYTE TRANSFORMATION; MALE; PRENATAL DIAGNOSIS; PRIORITY JOURNAL; SITUS INVERSUS;

ABNORMALITIES, MULTIPLE; ADULT; CASE REPORT; FATAL OUTCOME; FEMALE; FETUS; HOLOPROSENCEPHALY; HUMAN; INFANT, NEWBORN; JAW ABNORMALITIES; MALE; PREGNANCY; SITUS INVERSUS; ULTRASONOGRAPHY, PRENATAL;

EID: 0034118888     PISSN: 01487299     EISSN: None     Source Type: Journal    
DOI: 10.1002/(SICI)1096-8628(20000320)91:3<235::AID-AJMG16>3.0.CO;2-H     Document Type: Letter

References (13)