Congenital Anomalies

Activities and Announcement
pp. J3-J3(1)

Assisted reproductive technologies and birth defects
pp. 39-43(5)
Authors: Shiota, Kohei; Yamada, Shigehito

Methodological issues in the epidemiological study of the teratogenicity of drugs
pp. 44-51(8)
Authors: Källén, Bengt A.J.

Morphological differences in cardiovascular anomalies induced by bis-diamine between Sprague–Dawley and Wistar rats
pp. 52-58(7)
Authors: Fujino, Hidetoshi; Nakagawa, Masao; Nishijima, Setsuko; Okamoto, Nobuhiko; Hanato, Takashi; Watanabe, Noriko; Shirai, Takeaki; Kamiya, Hiroshi; Takeuchi, Yoshihiro

Clinical variability in a Japanese hereditary lymphedema type I family with an FLT4 mutation
pp. 59-61(3)
Authors: Mizuno, Seiji; Yamada, Yasukazu; Yamada, Kenichiro; Nomura, Noriko; Wakamatsu, Nobuaki

Refining chromosomal region critical for Down syndrome-related heart defects with a case of cryptic 21q22.2 duplication
pp. 62-64(3)
Authors: Kosaki, Rika; Kosaki, Kenjiro; Matsushima, Kazushige; Mitsui, Norimasa; Matsumoto, Naomichi; Ohashi, Hirofumi

Rubinstein-Taybi syndrome (RTS) with postaxial polydactyly of the foot: 4-year follow-up until improvement of dysbasia
pp. 65-66(2)
Authors: Muneuchi, Gan; Kogure, Tetsukuni; Sano, Norihisa; Hamamoto, Yusuke; Kishikawa, Yuka; Tamai, Motoki; Igawa, Hiroharu H

First case of L1CAM gene mutation identified in MASA syndrome in Asia
pp. 67-69(3)
Authors: Kanemura, Yonehiro; Takuma, Yuuichi; Kamiguchi, Hiroyuki; Yamasaki, Mami

Acardiac acephalic twin gestation with transposition of great arteries in pump twin
pp. 70-72(3)
Authors: Üstüner, Ik; imek, Erhan; Kahraman, Korhan; Cengiz, Bora; Koç, Acar