Analysis of ring chromosome 9 syndrome with fluorescence in situ hybridization

Chinese Journal of Medical Genetics

Volumn 27, Issue 5, 2010, Pages 559-562

  Ye, Zhi Chun ^a   Zhu, Xing Yuan ^a   Zhao, Rui ^a   He, Xin Yu ^a   Zhang, Hui Jia ^b   Li, Li Ping ^a   Zhu, Yi Min ^a  

^a HUNAN CHILDREN'S HOSPITAL   (China)

^b Rehabilitation Center   (China)

Author keywords

Clinical phenotypes; Dual color fluorescence in situ hybridization; Ring chromosome 9 syndrome

Indexed keywords

ARTICLE; CASE REPORT; CHROMOSOME 9P; CHROMOSOME 9Q; CHROMOSOME ANALYSIS; FLUORESCENCE IN SITU HYBRIDIZATION; GENETIC DISORDER; HUMAN; KARYOTYPE; PHENOTYPE; RING CHROMOSOME 9 SYNDROME; X CHROMOSOME;

CHROMOSOME DELETION; CHROMOSOME DISORDERS; CHROMOSOMES, HUMAN, PAIR 9; FEMALE; HUMANS; IN SITU HYBRIDIZATION, FLUORESCENCE; INFANT; KARYOTYPING; RING CHROMOSOMES;

EID: 78049315844     PISSN: 10039406     EISSN: None     Source Type: Journal    
DOI: 10.3760/cma.j.issn.1003-9406.2010.05.018     Document Type: Article

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