Comparative genomic hybridisation in mentally retarded patients with dysmorphic features and a normal karyotype

Clinical Genetics

Volumn 60, Issue 3, 2001, Pages 212-219

  Joly, G ^a,c   Lapierre, J M ^a   Ozilou, C ^a   Gosset, P ^a   Aurias, A ^b   De Blois, M C ^a   Prieur, M ^a   Raoul, O ^a   Colleaux, L ^a   Munnich, A ^a   Romana, S P ^a   Vekemans, M ^a   Turleau, C ^a  

^a HÔPITAL NECKER ENFANTS MALADES   (France)

^b INSTITUT CURIE   (France)

^c HÔPITAL CHARLES NICOLLE   (France)

Author keywords

CGH; Dysmorphic features; Mental retardation; Subtle chromosome rearrangements

Indexed keywords

ADOLESCENT; ARTICLE; BODY DYSMORPHIC DISORDER; CHILD; CHROMOSOME ABERRATION; CLINICAL ARTICLE; CLINICAL STUDY; CLINICAL TRIAL; COHORT ANALYSIS; COMPARATIVE STUDY; CONTROLLED CLINICAL TRIAL; CONTROLLED STUDY; CYTOGENETICS; DNA HYBRIDIZATION; EVALUATION; FAMILY; FEMALE; FETUS; FLUORESCENCE IN SITU HYBRIDIZATION; GENE REARRANGEMENT; GENOME; HUMAN; INFANT; KARYOTYPE; MALE; MENTAL DEFICIENCY; MOLECULAR PROBE; PRIORITY JOURNAL; SCREENING; STANDARD; TELOMERE;

EID: 0034774605     PISSN: 00099163     EISSN: None     Source Type: Journal    
DOI: 10.1034/j.1399-0004.2001.600307.x     Document Type: Article

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