Cytogenetic and array CGH characterization of an intrachromosomal complex rearrangement of 4q in a patient with a 4q-phenotype

American Journal of Medical Genetics, Part A

Volumn 146, Issue 1, 2008, Pages 110-115

  Sensi, Alberto ^a   Prontera, Paolo ^a,b   Buldrini, Barbara ^a   Palma, Silvia ^a   Aiello, Vincenzo ^a   Gruppioni, Rita ^a   Calzolari, Elisa ^a   Volinia, Stefano ^a   Martini, Alessandro ^a  

^a UNIVERSITY OF FERRARA   (Italy)

^b UNIVERSITY OF PERUGIA   (Italy)

Author keywords

4q syndrome; Array CGH; Chromosome 4; Complex intrachromosomal rearrangement; Deletion; Duplication

Indexed keywords

ARTICLE; CASE REPORT; CHILD; CHROMOSOME 4Q; CHROMOSOME DELETION 4; CHROMOSOME REARRANGEMENT; COMPARATIVE GENOMIC HYBRIDIZATION; CRANIOFACIAL MALFORMATION; CYTOGENETICS; DNA PROBE; FLUORESCENCE IN SITU HYBRIDIZATION; HUMAN; MULTIPLE MALFORMATION SYNDROME; PHENOTYPE; PRIORITY JOURNAL;

ABNORMALITIES, MULTIPLE; CHILD, PRESCHOOL; CHROMOSOME BANDING; CHROMOSOME DELETION; CHROMOSOMES, HUMAN, PAIR 4; CYTOGENETIC ANALYSIS; DNA; GENE DUPLICATION; GENE REARRANGEMENT; HUMANS; IN SITU HYBRIDIZATION, FLUORESCENCE; KARYOTYPING; MALE; NUCLEIC ACID HYBRIDIZATION; PHENOTYPE; SYNDROME;

EID: 37549055744     PISSN: 15524825     EISSN: 15524833     Source Type: Journal    
DOI: 10.1002/ajmg.a.32059     Document Type: Article

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