Patient with del(12)(q12q13.12) manifesting abnormalities compatible with Noonan syndrome

American Journal of Medical Genetics

Volumn 75, Issue 4, 1998, Pages 416-418

  Tonoki, Hidefumi ^a   Saitoh, Shinji ^a   Kobayashi, Kunihiko ^a  

^a HOKKAIDO UNIVERSITY   (Japan)

Author keywords

Chromosome 12; Multiple congenital anomaly; Noonan syndrome locus

Indexed keywords

ARTICLE; CASE REPORT; CHILD; CHROMOSOME DELETION; CLINICAL EXAMINATION; GENE LOCUS; GENETIC LINKAGE; HUMAN; INTRAUTERINE GROWTH RETARDATION; KARYOTYPE; MALE; MENTAL DEFICIENCY; NOONAN SYNDROME; PRIORITY JOURNAL; SYNDROME DELINEATION;

CHILD, PRESCHOOL; CHROMOSOMES, HUMAN, PAIR 12; GENE DELETION; HUMANS; JAPAN; KARYOTYPING; MALE; MENTAL RETARDATION; NOONAN SYNDROME; PHENOTYPE; TRANSLOCATION, GENETIC;

EID: 0032477907     PISSN: 01487299     EISSN: None     Source Type: Journal    
DOI: 10.1002/(SICI)1096-8628(19980203)75:4<416::AID-AJMG13>3.0.CO;2-R     Document Type: Article

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