Mohr syndrome in two sisters: Prenatal diagnosis in a 22-week-old fetus with post-mortem findings in both

Prenatal Diagnosis

Volumn 19, Issue 9, 1999, Pages 827-831

  Balci, Sevim ^a,b   Güler, Gülnur ^a   Kale, Gülsev ^a   Söylemezoǧlu, Figen ^a   Besim, Aytekin ^a  

^a HACETTEPE UNIVERSITY   (Turkey)

^b NONE   (Turkey)

Author keywords

Dandy Walker malformation; Mohr syndrome; Natal teeth; Oral facial digital syndrome type II; Prenatal diagnosis

Indexed keywords

ARTICLE; AUTOPSY; AUTOSOMAL RECESSIVE INHERITANCE; CASE REPORT; CONGENITAL HEART MALFORMATION; CONSANGUINITY; CORPUS CALLOSUM AGENESIS; DYSOSTOSIS; FEMALE; FETUS; GESTATIONAL AGE; HUMAN; LUNG MALFORMATION; MOHR SYNDROME; NEWBORN; OLFACTORY NERVE; PES EQUINOVARUS; POLYDACTYLY; PRENATAL DIAGNOSIS; PRIORITY JOURNAL; THUMB MALFORMATION; TOOTH MALFORMATION;

AUTOPSY; CONSANGUINITY; FEMALE; GENES, RECESSIVE; GESTATIONAL AGE; HUMANS; INFANT, NEWBORN; OROFACIODIGITAL SYNDROMES; ULTRASONOGRAPHY, PRENATAL;

EID: 0344604276     PISSN: 01973851     EISSN: None     Source Type: Journal    
DOI: 10.1002/(SICI)1097-0223(199909)19:9<827::AID-PD644>3.0.CO;2-E     Document Type: Article

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