De novo trisomy 20p of paternal origin

American Journal of Medical Genetics, Part A

Volumn 143, Issue 10, 2007, Pages 1100-1103

  Chaabouni, Myriam ^a   Turleau, Catherine ^b   Karboul, Lotfi ^c   Jemaa, Lamia Ben ^a   Maazoul, Faouzi ^a   Attié Bitach, Tania ^b   Romana, Serge ^b   Chaabouni, Habiba ^a  

^a UNIVERSITY OF TUNIS EL MANAR   (Tunisia)

^b HÔPITAL NECKER ENFANTS MALADES   (France)

^c CHILDREN S HOSPITAL   (Tunisia)

Author keywords

De novo; Pure; Trisomy 20p

Indexed keywords

APGAR SCORE; ARTICLE; CASE REPORT; CHROMOSOME 20; CHROMOSOME REARRANGEMENT; CONGENITAL HEART MALFORMATION; COORDINATION DISORDER; CRYPTORCHISM; DEVELOPMENTAL DISORDER; FACE DYSMORPHIA; FLUORESCENCE IN SITU HYBRIDIZATION; HEART MURMUR; HEART VENTRICLE SEPTUM DEFECT; HUMAN; HYPOSPADIAS; KARYOTYPE; KARYOTYPE 46,XY; KYPHOSIS; MALE; MENTAL DEFICIENCY; MUSCULOSKELETAL SYSTEM MALFORMATION; PHENOTYPE; PREAXIAL HEXADACTYLY; PRESCHOOL CHILD; PRIORITY JOURNAL; TRISOMY; TRISOMY 20P;

CHILD, PRESCHOOL; CHROMOSOME BANDING; CHROMOSOMES, HUMAN, PAIR 20; FACIAL ASYMMETRY; FATHERS; FINGERS; HUMANS; IN SITU HYBRIDIZATION, FLUORESCENCE; MALE; POLYDACTYLY; TRISOMY;

EID: 34248186060     PISSN: 15524825     EISSN: 15524833     Source Type: Journal    
DOI: 10.1002/ajmg.a.31704     Document Type: Article

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