SCOPUS 정보 검색 플랫폼

Volumn 24, Issue 2, 2001, Pages 111-116

Relationship between clinical and genetic features in 'inverted duplicated chromosome 15' patients

(8) Borgatti, Renato a Piccinelli, Paolo b Passoni, Davide a Dalprà, Leda c Miozzo, Monica c Micheli, Roberto d Gagliardi, Chiara a Balottin, Umberto b

a SCIENTIFIC INSTITUTE (Italy)

b UNIVERSITY OF INSUBRIA (Italy)

c UNIVERSITY OF MILAN (Italy)

d Brescia General Hospital (Italy)

Author keywords

[No Author keywords available]

Indexed keywords

ARTICLE; AUTISM; BEHAVIOR DISORDER; CHILD; CHROMOSOME 15; CHROMOSOME DUPLICATION; CHROMOSOME INVERSION; CLINICAL ARTICLE; CLINICAL FEATURE; CYTOGENETICS; FEMALE; GENETIC DISORDER; HUMAN; KARYOTYPE; MALE; MARKER CHROMOSOME; MENTAL DEFICIENCY; MENTAL DISEASE; NEUROLOGIC DISEASE; POLYMERASE CHAIN REACTION; PRIORITY JOURNAL; SEIZURE;

ADOLESCENT; AUTISTIC DISORDER; CHILD; CHILD DEVELOPMENT DISORDERS, PERVASIVE; CHILD, PRESCHOOL; CHROMOSOME ABERRATIONS; CHROMOSOME DISORDERS; CHROMOSOMES, HUMAN, PAIR 15; EPILEPSY; GENES, DUPLICATE; GENOTYPE; HUMANS; MALE; MENTAL RETARDATION; MICROSATELLITE REPEATS; PHENOTYPE; POLYMORPHISM, GENETIC; SEVERITY OF ILLNESS INDEX; SYNDROME;

EID: 0035057465 PISSN: 08878994 EISSN: None Source Type: Journal
DOI: 10.1016/S0887-8994(00)00244-7 Document Type: Article

Times cited : (70)

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