22q11 deletion in DGS/VCFS monozygotic twins with discordant phenotypes

Genetic Counseling

Volumn 10, Issue 1, 1999, Pages 43-49

  Vincent, M C ^a   Heitz, F ^b   Tricoire, J ^b   Bourrouillou, G ^a   Kuhlein, E ^c   Rolland, M ^b   Calvas, P ^a,c  

^a UNIVERSITÉ DE TOULOUSE   (France)

^b HÔPITAL DES ENFANTS   (France)

^c CHU PURPAN   (France)

Author keywords

22q11; Deletion; DiGeorge syndrome; Twins

Indexed keywords

BLOOD TRANSFUSION REACTION; CASE REPORT; CHROMOSOME 22Q; CHROMOSOME DELETION; CONFERENCE PAPER; CONGENITAL HEART MALFORMATION; DIGEORGE SYNDROME; DNA DETERMINATION; ENVIRONMENTAL FACTOR; FEMALE; FLUORESCENCE IN SITU HYBRIDIZATION; HEREDITY; HUMAN; HUMAN CELL; MONOZYGOTIC TWINS; MOSAICISM; NEWBORN; PHENOTYPE; POLYMERASE CHAIN REACTION; SOMATIC MUTATION;

ABNORMALITIES, MULTIPLE; ADULT; AORTIC COARCTATION; CHROMOSOME DELETION; CHROMOSOMES, HUMAN, PAIR 22; DIGEORGE SYNDROME; DISEASES IN TWINS; FACIES; FEMALE; FETAL GROWTH RETARDATION; GENOTYPE; HUMANS; IN SITU HYBRIDIZATION, FLUORESCENCE; INFANT, NEWBORN; PHENOTYPE; PREGNANCY; TWINS, MONOZYGOTIC; VARIATION (GENETICS); VELOPHARYNGEAL INSUFFICIENCY;

EID: 0033024723     PISSN: 10158146     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Conference Paper

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