Fryns syndrome phenotype and trisomy 22

American Journal of Medical Genetics

Volumn 61, Issue 1, 1996, Pages 68-70

  Ladonne, Jean Marie ^a   Gaillard, Dominique ^a   Carré Pigeon, Frédérique ^a   Gabriel, René ^a  

^a HÔPITAL MAISON BLANCHE   (France)

Author keywords

diaphragmatic hernia; Fryns syndrome; human chromosomes; multiple malformations; trisomy 22

Indexed keywords

ARTICLE; BONE RADIOGRAPHY; CASE REPORT; CHROMOSOME 22; CONGENITAL DIAPHRAGM HERNIA; CYTOGENETICS; ECHOGRAPHY; FETUS; FRYNS SYNDROME; HUMAN; HUMAN CELL; INTRAUTERINE GROWTH RETARDATION; KARYOTYPING; MALE; PHENOTYPE; PRIORITY JOURNAL; TRISOMY;

ADULT; CHROMOSOMES, HUMAN, PAIR 22; FACE; FEMALE; FETAL GROWTH RETARDATION; FINGERS; HERNIA, DIAPHRAGMATIC; HUMANS; HYPERTENSION; INFANT, NEWBORN; KARYOTYPING; MALE; NAILS, MALFORMED; PHENOTYPE; PREGNANCY; PREGNANCY COMPLICATIONS, CARDIOVASCULAR; SYNDROME; TRISOMY;

EID: 0030061620     PISSN: 01487299     EISSN: None     Source Type: Journal    
DOI: 10.1002/(SICI)1096-8628(19960102)61:1<68::AID-AJMG13>3.0.CO;2-U     Document Type: Article

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