An emerging phenotype of interstitial 15q25.2 microdeletions: Clinical report and review

American Journal of Medical Genetics, Part A

Volumn 158 A, Issue 12, 2012, Pages 3182-3189

  Palumbo, Orazio ^a   Palumbo, Pietro ^a,b   Palladino, Teresa ^a   Stallone, Raffaella ^a   Miroballo, Mattia ^a   Piemontese, Maria Rosaria ^a   Zelante, Leopoldo ^a   Carella, Massimo ^a  

^a CASA SOLLIEVO DELLA SOFFERENZA HOSPITAL   (Italy)

^b UNIVERSITY OF BARI   (Italy)

Author keywords

15q25.2; New microdeletion syndrome; Smallest region of overlap

Indexed keywords

ANXIETY; ARTICLE; AUTISM; BEHAVIOR DISORDER; CASE REPORT; CHILD; CHROMOSOME 15Q; CHROMOSOME DELETION 15Q25; CHROMOSOME REARRANGEMENT; CLINICAL FEATURE; CONGENITAL MALFORMATION; DEVELOPMENTAL DISORDER; DISEASE SEVERITY; FEMALE; HEMIZYGOTE; HUMAN; HYPERACTIVITY; INTERSTITIAL CHROMOSOME DELETION; MICRODELETION SYNDROME; MOLECULAR GENETICS; NUCLEOTIDE SEQUENCE; PARENT; PHENOTYPE; PRIORITY JOURNAL; PSYCHOMOTOR DISORDER; SCHOOL CHILD; SINGLE NUCLEOTIDE POLYMORPHISM; SPEECH DISORDER; SYNDROME; UNINDEXED SEQUENCE;

EID: 84870247315     PISSN: 15524825     EISSN: 15524833     Source Type: Journal    
DOI: 10.1002/ajmg.a.35631     Document Type: Article

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