Neurodevelopmental profile of a new dysmorphic syndrome associated with submicroscopic partial deletion of 1p36.3

Developmental Medicine and Child Neurology

Volumn 42, Issue 3, 2000, Pages 201-206

  Knight Jones, Eve ^a   Knight, Samantha ^b   Heussler, Helen ^c   Regan, Regina ^b   Flint, Jonathan ^b   Martin, Katherine ^a  

^a NOTTINGHAM CITY HOSPITAL   (United Kingdom)

^b JOHN RADCLIFFE HOSPITAL   (United Kingdom)

^c QUEEN S MEDICAL CENTRE   (United Kingdom)

Author keywords

[No Author keywords available]

Indexed keywords

ADOLESCENT; ADULT; ARTICLE; BODY POSTURE; CASE REPORT; CHILD; CHROMOSOME 1P; CHROMOSOME ANALYSIS; CHROMOSOME ARM; CLINICAL FEATURE; DEVELOPMENTAL DISORDER; DISEASE SEVERITY; EPILEPSY; EYE MALFORMATION; FACE DYSMORPHIA; FACIES; FEMALE; FLUORESCENCE IN SITU HYBRIDIZATION; GENE DELETION; HUMAN; INFANT; LEARNING DISORDER; MALE; MICROCEPHALY; MIDFACE HYPOPLASIA; MOTOR DYSFUNCTION; MUSCLE HYPOTONIA; NERVE CELL DIFFERENTIATION; NEWBORN; PARTIAL MONOSOMY; PHENOTYPE; PRIORITY JOURNAL; TELOMERE; VISUAL DISORDER;

ABNORMALITIES, MULTIPLE; CHILD, PRESCHOOL; CHROMOSOMES, HUMAN, PAIR 1; FEMALE; GENE DELETION; HUMANS; IN SITU HYBRIDIZATION, FLUORESCENCE; INFANT; LEARNING DISORDERS; MALE; SYNDROME;

EID: 0034057704     PISSN: 00121622     EISSN: None     Source Type: Journal    
DOI: 10.1017/S0012162200000347     Document Type: Article

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