Familial factors and hearing impairment modulate the neuromotor phenotype in Turner syndrome

European Journal of Pediatrics

Volumn 162, Issue 1, 2003, Pages 30-35

  Haverkamp, Fritz ^a   Keuker, Tanja ^a   Woelfle, Joachim ^a   Kaiser, Gundi ^a   Zerres, Klaus ^c   Rietz, Christian ^b   Ruenger, Michaela ^a  

^a UNIVERSITY HOSPITAL BONN   (Germany)

^b UNIVERSITY OF BONN   (Germany)

^c RWTH AACHEN UNIVERSITY   (Germany)

Author keywords

Familial covariance; Genotype phenotype relation; Hypergonadotropic hypogonadism; Mosaicism; Otitis media

Indexed keywords

ADOLESCENT; ARTICLE; CHILD; CHROMOSOME MOSAICISM; CLINICAL ARTICLE; CORRELATION ANALYSIS; COVARIANCE; FEMALE; HEARING IMPAIRMENT; HUMAN; HYPERGONADOTROPIC HYPOGONADISM; MALE; MOTONEURON; MOTOR ACTIVITY; OTITIS MEDIA; PHENOTYPE; PREDICTION; PRIORITY JOURNAL; RISK FACTOR; SENSORIMOTOR FUNCTION; TURNER SYNDROME; AGE; GENETICS; HEARING LOSS; HYPOGONADISM; MOSAICISM; NEUROLOGIC EXAMINATION; NEUROMUSCULAR DISEASE; OVARY; PATHOPHYSIOLOGY; PRESCHOOL CHILD; RECURRENT DISEASE;

ADOLESCENT; AGE FACTORS; CHILD; CHILD, PRESCHOOL; FEMALE; HEARING LOSS; HUMANS; HYPOGONADISM; MOSAICISM; NEUROLOGIC EXAMINATION; NEUROMUSCULAR DISEASES; OTITIS MEDIA; OVARY; PHENOTYPE; RECURRENCE; TURNER SYNDROME;

EID: 0037214089     PISSN: 03406199     EISSN: None     Source Type: Journal    
DOI: 10.1007/s00431-002-1087-5     Document Type: Article

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