Interstitial deletion of the short arm of chromosome 1: Attempt to establish a clinical phenotype (46,XX,del (1)(p22p32))

American Journal of Medical Genetics

Volumn 118 A, Issue 2, 2003, Pages 176-179

  Mircher, Clotilde ^a,d   Rethore, Marie Odile ^a   Lespinasse, James ^b   Fert Ferrer, Sandra ^b   Lundsteen, Claes ^c   Kirchoff, Maria ^c  

^a Ctr Med Jerome Lejeune   (France)

^b GENERAL HOSPITAL   (France)

^c University of Copenhagen   (Denmark)

^d Institut Jerome Lejeune   (France)

Author keywords

Chromosome 1p; Interstitial deletion

Indexed keywords

ARTICLE; CASE REPORT; CHILD; CHROMOSOME 1P; COMPARATIVE GENOMIC HYBRIDIZATION; CYTOGENETICS; DEVELOPMENTAL DISORDER; FEMALE; FLUORESCENCE IN SITU HYBRIDIZATION; HUMAN; HUMAN CELL; INTERSTITIAL CHROMOSOME DELETION; KARYOTYPE 46,XX; MENTAL RETARDATION MALFORMATION SYNDROME; PHENOTYPE; PRIORITY JOURNAL; CHROMOSOME 1; CHROMOSOME DELETION; GENETICS; KARYOTYPING; PATHOLOGY; PRESCHOOL CHILD; REVIEW;

CHILD, PRESCHOOL; CHROMOSOME DELETION; CHROMOSOMES, HUMAN, PAIR 1; DEVELOPMENTAL DISABILITIES; FEMALE; HUMANS; KARYOTYPING; PHENOTYPE;

EID: 0037487185     PISSN: 15524825     EISSN: None     Source Type: Journal    
DOI: 10.1002/ajmg.a.10052     Document Type: Article

References (13)

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