Paternally derived der(7)t(Y;7)(p11.1∼11.2;p22.3)dn in a mosaic case with Turner syndrome

European Journal of Medical Genetics

Volumn 52, Issue 4, 2009, Pages 207-210

  Polityko, Anna D ^a,b   Khurs, Olga M ^b   Kulpanovich, Anna I ^b   Mosse, Konstantin A ^b   Solntsava, Angelica V ^c   Rumyantseva, Natalia V ^b   Naumchik, Irina V ^b   Liehr, Thomas ^a   Weise, Anja ^a   Mkrtchyan, Hasmik ^a  

^a Institute of Human Genetics and Anthropology   (Germany)

^b National Medical Center 'Mother and Child'   (Belarus)

^c BELARUSIAN STATE MEDICAL UNIVERSITY   (Belarus)

Author keywords

Gonosome autosome translocation; Molecular cytogenetics; Mosaic; Parental origin; Turner syndrome

Indexed keywords

ESTRADIOL; FOLLITROPIN; HYDROCORTISONE; LUTEINIZING HORMONE; PROGESTERONE; PROLACTIN; SOMATOMEDIN; TESTOSTERONE; THYROTROPIN;

ARTICLE; BICUSPID AORTIC VALVE; CASE REPORT; CHILD; CHROMOSOME 7; CHROMOSOME REARRANGEMENT; CHROMOSOME TRANSLOCATION; CLINICAL EXAMINATION; CYTOGENETICS; ECHOCARDIOGRAPHY; FEMALE; FLUORESCENCE IN SITU HYBRIDIZATION; GROWTH RETARDATION; HISTOLOGY; HUMAN; HYPERACTIVITY; KARYOTYPE 45,X; LAPAROSCOPY; MICROSATELLITE INSTABILITY; MOLECULAR GENETICS; MOSAICISM; PATENT DUCTUS ARTERIOSUS; PHENOTYPE; PRESCHOOL CHILD; SCHOOL CHILD; SEXUAL DEVELOPMENT; SHORT STATURE; SYSTOLIC HEART MURMUR; TURNER SYNDROME; X CHROMOSOME; Y CHROMOSOME;

CHILD; CHROMOSOME DELETION; CHROMOSOMES, HUMAN, PAIR 7; CHROMOSOMES, HUMAN, X; CHROMOSOMES, HUMAN, Y; FATHERS; FEMALE; HAPLOTYPES; HUMANS; IN SITU HYBRIDIZATION, FLUORESCENCE; KARYOTYPING; MALE; MICROSATELLITE REPEATS; MOSAICISM; TRANSLOCATION, GENETIC; TURNER SYNDROME;

EID: 67650635157     PISSN: 17697212     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.ejmg.2009.03.016     Document Type: Article

References (19)

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