Cryptic 1p36.3/6q25.2 translocation in three generations ascertained through a foetus with IUGR and cerebral malformations

Prenatal Diagnosis

Volumn 23, Issue 10, 2003, Pages 819-823

  Cavani, S ^a   Perfumo, C ^a   Faravelli, F ^a   Malacarne, M ^a   Sogliani, M ^b   Piombo, G ^a   Zerega, G ^a   Zucca, M ^a   Bricarelli, F Dagna ^a   Pierluigi, M ^a  

^a GALLIERA HOSPITAL   (Italy)

^b G GASLINI INSTITUTE   (Italy)

Author keywords

Cerebral malformations; FISH; Monosomy 1p; Prenatal diagnosis; Trisomy 6q

Indexed keywords

ARTICLE; BRAIN MALFORMATION; CASE REPORT; CHROMOSOME 1P; CHROMOSOME 6Q; CHROMOSOME TRANSLOCATION; CYTOGENETICS; FETUS; FLUORESCENCE IN SITU HYBRIDIZATION; HUMAN; INTRAUTERINE GROWTH RETARDATION; PEDIGREE ANALYSIS; PRENATAL DIAGNOSIS; PRIORITY JOURNAL;

ABNORMALITIES, MULTIPLE; ADULT; CHROMOSOMES, HUMAN, PAIR 1; CHROMOSOMES, HUMAN, PAIR 6; DIAGNOSIS, DIFFERENTIAL; FAMILY; FATAL OUTCOME; FEMALE; FETAL GROWTH RETARDATION; GENETIC COUNSELING; HUMANS; INFANT, NEWBORN; MALE; PEDIGREE; PREGNANCY; PREGNANCY TRIMESTER, THIRD; PRENATAL DIAGNOSIS; TELENCEPHALON; TRANSLOCATION, GENETIC;

EID: 10744225628     PISSN: 01973851     EISSN: None     Source Type: Journal    
DOI: 10.1002/pd.678     Document Type: Article

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