Correlation of clinical phenotype with a pericentric inversion of chromosome 9 and genetic counseling

Saudi Medical Journal

Volumn 29, Issue 7, 2008, Pages 946-951

  Dermihan, Osman ^a   Pazarbasi, Ayfer ^a   Suleymanova Karahan, Dilara ^a   Tanriverdi, Nilgun ^a   Kilinc, Yurdanur ^a  

^a CUKUROVA UNIVERSITY   (Turkey)

Author keywords

[No Author keywords available]

Indexed keywords

ARTICLE; CHROMOSOME 11; CHROMOSOME 9; CHROMOSOME ANALYSIS; CLINICAL FEATURE; CONTROLLED STUDY; CORRELATION ANALYSIS; FEMALE; GENE LOCUS; GENETIC ASSOCIATION; GENETIC COUNSELING; GENETIC SUSCEPTIBILITY; HETEROZYGOTE DETECTION; HUMAN; INCIDENCE; KARYOTYPING; MAJOR CLINICAL STUDY; MALE; MENTAL DEFICIENCY; MOLECULAR CLONING; PERICENTRIC CHROMOSOME INVERSION; PHENOTYPE; SPONTANEOUS ABORTION; TURKEY (REPUBLIC);

ADULT; CHILD; CHROMOSOMES, HUMAN, PAIR 9; COHORT STUDIES; FEMALE; GENETIC COUNSELING; GENETIC PREDISPOSITION TO DISEASE; HETEROZYGOTE; HUMANS; INVERSION, CHROMOSOME; KARYOTYPING; MALE; PHENOTYPE; RETROSPECTIVE STUDIES; TURKEY;

EID: 57349106557     PISSN: 03795284     EISSN: 16583175     Source Type: Journal    
DOI: None     Document Type: Article

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