Prenatal diagnosis of holoprosencephaly (HPE) in a fetus with a recombinant (18)dup(18q)inv(18)(p11.31q11.2)mat

Prenatal Diagnosis

Volumn 20, Issue 12, 2000, Pages 947-949

  Leonard, Norma J ^a,b   Tomkins, Darrell J ^a   Demianczuk, Nestor ^a  

^a UNIVERSITY OF ALBERTA   (Canada)

^b UNIVERSITY OF ALBERTA HOSPITAL   (Canada)

Author keywords

18p; Chromosome; Holoprosencephaly (HPE); Prenatal; Ultrasound

Indexed keywords

AMNIOCENTESIS; ARTICLE; CHROMOSOME 18P; CHROMOSOME 18Q; CHROMOSOME BREAKAGE; CHROMOSOME REARRANGEMENT; CLINICAL FEATURE; CYTOGENETICS; DIAGNOSTIC IMAGING; FETUS; FETUS ECHOGRAPHY; GESTATIONAL AGE; HOLOPROSENCEPHALY; HUMAN; HYPOTELORISM; ISOCHROMOSOME; KARYOTYPE 46,XX; PERICENTRIC CHROMOSOME INVERSION; PRIORITY JOURNAL; THERAPEUTIC ABORTION;

ADULT; AMNIOCENTESIS; CHROMOSOMES, HUMAN, PAIR 18; FEMALE; HOLOPROSENCEPHALY; HUMANS; INVERSION, CHROMOSOME; PREGNANCY; ULTRASONOGRAPHY, PRENATAL;

EID: 0034530019     PISSN: 01973851     EISSN: None     Source Type: Journal    
DOI: 10.1002/1097-0223(200012)20:12<947::AID-PD957>3.0.CO;2-X     Document Type: Article

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