Chromosome 1 syndrome and hearing loss: An unusual case;Chromosom-1q-syndrom und innenohrschwerhörigkeit: Ein ungewöhnlicher fall

Laryngo- Rhino- Otologie

Volumn 85, Issue 4, 2006, Pages 279-282

  Schwemmle, Cornelia ^a   Schulze, B ^b   Ptok, M ^a  

^a HANNOVER MEDICAL SCHOOL   (Germany)

^b Institut für Humangenetik   (Germany)

Author keywords

Auditory evoked potential (AEP); Chromosome 1q deletion; Hearing loss; Pedaudiology

Indexed keywords

ARTICLE; AUDIOMETRY; BRACHYCEPHALY; BRAIN STEM RESPONSE; CAMPTODACTYLY; CASE REPORT; CHROMOSOME 15 SYNDROME; CHROMOSOME 1Q; CHROMOSOME ARM; CHROMOSOME DELETION; CHROMOSOME DISORDER; CLEFT LIP PALATE; CLINODACTYLY; DISEASE SEVERITY; EARLY DIAGNOSIS; EYEBROW; FOOT MALFORMATION; GENITAL MALFORMATION; GROWTH RETARDATION; HAND MALFORMATION; HEARING LOSS; HEART DISEASE; HERNIA; HUMAN; HYPOTROPHY; KIDNEY DISEASE; MALE; MENTAL DEFICIENCY; MORPHOLOGY; PERCEPTION DEAFNESS; PHENOTYPE; POSTNATAL GROWTH; PRENATAL GROWTH; PRIORITY JOURNAL; PSYCHOMOTOR DISORDER; RARE DISEASE; SCALP HAIR; SCHOOL CHILD; SCOLIOSIS; SYMPTOMATOLOGY;

ABNORMALITIES, MULTIPLE; AUDIOMETRY, EVOKED RESPONSE; CHILD; CHROMOSOME DELETION; CHROMOSOME MAPPING; CHROMOSOMES, HUMAN, PAIR 1; CRANIOFACIAL ABNORMALITIES; DEAFNESS; EVOKED POTENTIALS, AUDITORY, BRAIN STEM; FOLLOW-UP STUDIES; HUMANS; MALE; MENTAL RETARDATION; PHENOTYPE;

EID: 33645795984     PISSN: 09358943     EISSN: None     Source Type: Journal    
DOI: 10.1055/s-2005-870304     Document Type: Article

References (20)

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