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	221.	Medical cost savings in Sakado City and worldwide achieved by preventing disease by folic acid fortification. [electronic resource] by Kagawa, Yasuo Hiraoka, Mami Kageyama, Mitsuyo Kontai, Yoshiko Yurimoto, Mayumi Nishijima, Chiharu Sakamoto, Kaori Producer: 20180830 In: Congenital anomalies vol. 57 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	222.	Contiguous gene deletion neighboring TWIST1 identified in a patient with Saethre-Chotzen syndrome associated with neurodevelopmental delay: Possible contribution of HDAC9. [electronic resource] by Shimbo, Hiroko Oyoshi, Tatsuki Kurosawa, Kenji Producer: 20180830 In: Congenital anomalies vol. 58 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	223.	A Say-Barber-Biesecker-Young-Simpson variant of Ohdo syndrome with a KAT6B 10-base pair palindromic duplication: A recurrent mutation causing a severe phenotype mixed with genitopatellar syndrome. [electronic resource] by Niida, Yo Mitani, Yusuke Kuroda, Mondo Yokoi, Ayano Nakagawa, Hiroyasu Kato, Akiko Producer: 20180207 In: Congenital anomalies vol. 57 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	224.	Preconceptional folic acid supplementation in Japan. [electronic resource] by Hirahara, Fumiki Hamanoue, Haruka Kurasawa, Kentaro Producer: 20180830 In: Congenital anomalies vol. 57 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	225.	Proposal for supplemental intake of folic acid to reduce the risk of neural tube defects. [electronic resource] Producer: 20180830 In: Congenital anomalies vol. 57 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	226.	Novel FBN1 mutation in a family with inherited Marfan Syndrome: p.Cys2672Arg. [electronic resource] by Cetinkaya, Arda Karaman, Ali Mutlu, Mehmet Burak Yavuz, Taner Producer: 20180830 In: Congenital anomalies vol. 58 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	227.	Novel A178P mutation in SLC16A2 in a patient with Allan-Herndon-Dudley syndrome. [electronic resource] by Yamamoto, Toshiyuki Lu, Yongping Nakamura, Ryoko Shimojima, Keiko Kira, Ryutaro Producer: 20190829 In: Congenital anomalies vol. 58 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	228.	D40/KNL1/CASC5 and autosomal recessive primary microcephaly. [electronic resource] by Takimoto, Masato Producer: 20180830 In: Congenital anomalies vol. 57 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	229.	Interkinetic nuclear migration in the tracheal and esophageal epithelia of the mouse embryo: Possible implications for tracheo-esophageal anomalies. [electronic resource] by Kaneda, Ryo Saeki, Yuko Getachew, Dereje Matsumoto, Akihiro Furuya, Motohide Ogawa, Noriko Motoya, Tomoyuki Rafiq, Ashiq M Jahan, Esrat Udagawa, Jun Hashimoto, Ryuju Otani, Hiroki Producer: 20180815 In: Congenital anomalies vol. 58 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	230.	Developmental mechanisms of the tympanic membrane in mammals and non-mammalian amniotes. [electronic resource] by Takechi, Masaki Kitazawa, Taro Hirasawa, Tatsuya Hirai, Tamami Iseki, Sachiko Kurihara, Hiroki Kuratani, Shigeru Producer: 20161213 In: Congenital anomalies vol. 56 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	231.	Exome sequencing identifies a novel nonsense mutation of HOXD13 in a Chinese family with synpolydactyly. [electronic resource] by Wang, Bo Li, Niu Geng, Juan Wang, Zhigang Fu, Qihua Wang, Jian Xu, Yunlan Producer: 20170206 In: Congenital anomalies vol. 57 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	232.	Induction of a thoracolumbar supernumerary rib in rat developmental toxicity studies: A short discussion on the critical window. [electronic resource] by Kuwagata, Makiko Senuma, Mika Todoroki, Mai Kumagai, Fumiaki Kumamoto, Takayuki Ogawa, Tetsuo Producer: 20200326 In: Congenital anomalies vol. 59 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	233.	Establishment of a simple and rapid method to detect MECP2 duplications using digital polymerase chain reaction. [electronic resource] by Imaizumi, Taichi Yamamoto-Shimojima, Keiko Yamamoto, Hitoshi Yamamoto, Toshiyuki Producer: 20200619 In: Congenital anomalies vol. 60 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	234.	Survival in double aneuploidy involving trisomy 18 and sex chromosome trisomy: A case report of a 27-month-old child and a review of the literature. [electronic resource] by Watabe, Takahide Koga, Hiroshi Producer: 20190708 In: Congenital anomalies vol. 59 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	235.	Zebrafish yolk sac microinjection of thalidomide for assessment of developmental toxicology. [electronic resource] by Mikami, Ikuko Takahashi, Yuka Koiwa, Junko Okamura, Mina Tanaka, Toshio Publication details: Congenital anomalies Mar 2020 In: Congenital anomalies vol. 60 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	236.	Risk factors for abdominal wall defects. [electronic resource] by Kapapa, Melanie Rieg, Teresa Henne-Bruns, Doris Serra, Alexandre Publication details: Congenital anomalies Mar 2020 In: Congenital anomalies vol. 60 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	237.	Intellectual disability and dysmorphic features in male siblings arising from a novel TAF1 mutation. [electronic resource] by Okamoto, Nobuhiko Arai, Hiroshi Onishi, Toshikazu Mizuguchi, Takeshi Matsumoto, Naomichi Producer: 20200619 In: Congenital anomalies vol. 60 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	238.	The Japanese Teratology Society declares "Folic Acid Awareness Day" and "Neural Tube Defect Prevention Month". [electronic resource] Producer: 20191211 In: Congenital anomalies vol. 59 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	239.	Prenatal sonographic findings and prognosis of craniosynostosis diagnosed during the fetal and neonatal periods. [electronic resource] by Harada, Aya Miyashita, Susumu Nagai, Ryuhei Makino, Shintaro Murotsuki, Jun Producer: 20191211 In: Congenital anomalies vol. 59 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	240.	Association between a common missense variant in LOXL3 gene and the risk of non-syndromic cleft palate. [electronic resource] by Khan, Mohammad Faisal J Little, Julian Mossey, Peter A Steegers-Theunissen, Régine P M Bonsi, Martina Bassi Andreasi, Rita Rubini, Michele Producer: 20181015 In: Congenital anomalies vol. 58 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)

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