Paternally inherited duplications of 11p15.5 and Beckwith-Wiedemnann syndrome

Journal of Medical Genetics

Volumn 34, Issue 10, 1997, Pages 819-826

  Slavotinek, Anne ^a   Gaunt, Lorraine ^a   Donnai, Dian ^a  

^a ST MARY S HOSPITAL   (United Kingdom)

Author keywords

11p trisomy; Beckwith Wiedemann syndrome; Duplication 11p

Indexed keywords

ADOLESCENT; ARTICLE; BECKWITH WIEDEMANN SYNDROME; BIRTH WEIGHT; CASE REPORT; CHROMOSOME 11; CHROMOSOME 11P; CHROMOSOME 5; CHROMOSOME 5P; CHROMOSOME DUPLICATION; CHROMOSOME TRANSLOCATION; CLINICAL FEATURE; CRANIOFACIAL MALFORMATION; FACIES; FEMALE; HUMAN; HUMAN CELL; INHERITANCE; KARYOTYPE; MACROGLOSSIA; MALE; MONOSOMY; NEWBORN; PRENATAL GROWTH; PRESCHOOL CHILD; PRIORITY JOURNAL; RECIPROCAL CHROMOSOME TRANSLOCATION; SEQUENCE HOMOLOGY; TRISOMY;

ADOLESCENT; BECKWITH-WIEDEMANN SYNDROME; CHROMOSOMES, HUMAN, PAIR 11; CHROMOSOMES, HUMAN, PAIR 5; FATHERS; FEMALE; HUMANS; KARYOTYPING; MALE; MULTIGENE FAMILY; PEDIGREE; TRANSLOCATION, GENETIC;

EID: 0030823992     PISSN: 00222593     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Article

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