@article{oai:phoenix.repo.nii.ac.jp:00000643,
 author = {園田, 徹 and 金子, 政時 and 鮫島, 浩 and 池ノ上, 克 and 河野, 慶一郎 and ソノダ, トオル and カネコ, マサトキ and サメシマ, ヒロシ and イケノウエ, ツヨム and コウノ, ケイイチロウ and SONODA, Tohru and KANEKO, Masatoki and SAMESHIMA, Hiroshi and IKENOUE, Tsuyomu and KOUNO, Keiichiro},
 journal = {九州保健福祉大学研究紀要, Journal of Kyushu University of Health and Welfare},
 month = {Mar},
 note = {P(論文), We present triplet babies by a 46,XY,t(12;13)(q24.3;q32)father. The babies were the third pregnancy to healthy and unrelated parents. Conceived by fertility treatment (HMG-HCG therapy), they were born after a 31-week gestation by caesarean section. The first baby, a male infant, had a birth weight of 1,654g, and the same balanced translocation between chromosomes 12 and 13 as his father. The second baby, a female infant, with a birth weight of 878g died soon after her birth due to anencephaly. She showed a peculiar facial appearance accompanied by anencephaly including hypertelorism, narrow palpebral fissures, high nasal root, bulbous nose, micrognathia, and low-set ears. Her karyotype was 46,XX,der(12)t(12;i3) (q24.3;q32)pat, and she had a partial trisomy for 13q32→qter. The third baby, also female, had a birth weight of 1,446g and a normal karyotype. The phenotypes of the first and third babies were normal.},
 pages = {169--172},
 title = {不妊治療による46,XY,t(12;13)(q24.3;q32)の父親からの3胎},
 volume = {7},
 year = {2006},
 yomi = {ソノダ, トオル and カネコ, マサトキ and サメシマ, ヒロシ and イケノウエ, ツヨム and コウノ, ケイイチロウ}
}