A phenotypically normal liveborn male after prenatal diagnosis of trisomy 20 mosaicism

Journal of Obstetrics and Gynaecology Research

Volumn 23, Issue 3, 1997, Pages 301-305

  Hayashi, Satoshi ^a   Miharu, Norio ^a   He, Hu ^a   Honda, Hiroshi ^a   Samura, Osamu ^a   Nakaoka, Yoshiharu ^a   Ohama, Koso ^a  

^a HIROSHIMA UNIV SCHOOL OF MEDICINE   (Japan)

Author keywords

Fluorescence in situ hybridization (FISH); Prenatal diagnosis; Trisomy 20 mosaicism

Indexed keywords

AMNIOCENTESIS; ARTICLE; CASE REPORT; CHROMOSOME ANALYSIS; EMBRYONAL TISSUE; FETUS; FLUORESCENCE IN SITU HYBRIDIZATION; HUMAN; KARYOTYPE 46,XY; LYMPHOCYTE; MALE; MOSAICISM; NEWBORN; PHENOTYPE; PRENATAL DIAGNOSIS; TRISOMY; UMBILICAL CORD BLOOD;

EID: 0030761893     PISSN: 13418076     EISSN: None     Source Type: Journal    
DOI: 10.1111/j.1447-0756.1997.tb00849.x     Document Type: Article

References (7)

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