The del(2)(q32.2q33) deletion syndrome defined by clinical and molecular characterization of four patients

European Journal of Medical Genetics

Volumn 48, Issue 3, 2005, Pages 276-289

  Van Buggenhout, G ^a   Van Ravenswaaij Arts, C ^b   Mc Maas, N ^a   Thoelen, R ^a   Vogels, A ^a   Smeets, Dominique ^b   Salden, I ^a   Matthijs, G ^a   Fryns, J P ^a   Vermeesch, J R ^a  

^a UNIVERSITY OF LEUVEN   (Belgium)

^b RADBOUD UNIVERSITY MEDICAL CENTER   (Netherlands)

Author keywords

Array CGH; Behavioral problems; Chromosome 2; Interstitial deletion of chromosome 2; Mental retardation

Indexed keywords

ADULT; AGGRESSION; ANXIETY; ARTICLE; AUTOMUTILATION; BEHAVIOR DISORDER; BODY BUILD; CASE REPORT; CHILD; CHROMOSOME 2Q; CHROMOSOME DELETION; CLEFT PALATE; CLINICAL FEATURE; DACRYOCYSTITIS; FACE DYSMORPHIA; FEEDING DISORDER; FLUORESCENCE IN SITU HYBRIDIZATION; GAIT DISORDER; GENETIC DISORDER; GROWTH RETARDATION; HAIR; HUMAN; HYPERACTIVITY; INGUINAL HERNIA; INTRAUTERINE GROWTH RETARDATION; MACROGLOSSIA; MALE; MENTAL DEFICIENCY; MICROGNATHIA; PERSONALITY DISORDER; PHENOTYPE; POSTNATAL GROWTH; RESTLESSNESS; SLEEP DISORDER; WRINKLY SKIN SYNDROME;

ABNORMALITIES, MULTIPLE; ADOLESCENT; ADULT; CHILD; CHILD, PRESCHOOL; CHROMOSOME DELETION; CHROMOSOME DISORDERS; CHROMOSOMES, HUMAN, PAIR 2; DNA; HUMANS; IN SITU HYBRIDIZATION, FLUORESCENCE; MALE; MENTAL RETARDATION; OLIGONUCLEOTIDE ARRAY SEQUENCE ANALYSIS; SKIN DISEASES; SYNDROME;

EID: 25144494077     PISSN: 17697212     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.ejmg.2005.05.005     Document Type: Article

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