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	361.	Re-evaluation of lung to thorax transverse area ratio immediately before birth in predicting postnatal short-term outcomes of fetuses with isolated left-sided congenital diaphragmatic hernia: A single center analysis. [electronic resource] by Kido, Saki Hidaka, Nobuhiro Sato, Yuka Fujita, Yasuyuki Miyoshi, Kina Nagata, Kouji Taguchi, Tomoaki Kato, Kiyoko Producer: 20180921 In: Congenital anomalies vol. 58 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	362.	Association of single nucleotide polymorphisms in WNT genes with the risk of nonsyndromic cleft lip with or without cleft palate. [electronic resource] by Rafighdoost, Houshang Hashemi, Mohammad Asadi, Hossein Bahari, Gholamreza 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)
	363.	Coffin-Siris syndrome and cardiac anomaly with a novel SOX11 mutation. [electronic resource] by Okamoto, Nobuhiko Ehara, Eiji Tsurusaki, Yoshinori Miyake, Noriko Matsumoto, Naomichi Producer: 20180921 In: Congenital anomalies vol. 58 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	364.	Novel PORCN mutation in a severe case of Focal Dermal Hypoplasia. [electronic resource] by Ramirez-Botero, Andres Felipe Eichler, Sabrina Rolfs, Arndt Pachajoa, Harry Publication details: Congenital anomalies May 2016 In: Congenital anomalies vol. 56 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	365.	Unilateral occipital condylar dysplasia: 3-dimensional multidetector computed tomography and magnetic resonance findings. [electronic resource] by Lee, Do Hyung Je, Bo-Kyung Hong, Doran Kim, Sang-Dae Eun, So-Hee Producer: 20170206 In: Congenital anomalies vol. 56 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	366.	Clinical study of 459 polydactyly cases in China, 2010 to 2014. [electronic resource] by Xiang, Ying Bian, Jingxia Wang, Zhigang Xu, Yunlan Fu, Qihua Producer: 20170206 In: Congenital anomalies vol. 56 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	367.	Insights into 6q21-q22: Refinement of the critical region for acro-cardio-facial syndrome. [electronic resource] by Milani, Donatella Cagnoli, Giulia Anna Baccarin, Marco Alfei, Enrico Guerneri, Silvana Esposito, Susanna Publication details: Congenital anomalies Jul 2016 In: Congenital anomalies vol. 56 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	368.	Vesico-amniotic shunting for lower urinary tract obstruction in a fetus with VACTERL association. [electronic resource] by Kanasugi, Tomonobu Kikuchi, Akihiko Haba, Gen Sasaki, Yuri Isurugi, Chizuko Oyama, Rie Sugiyama, Toru Producer: 20170206 In: Congenital anomalies vol. 56 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	369.	Early prenatal detection of hypertrophic cardiomyopathy in Noonan syndrome: A case to remember. [electronic resource] by Han, Jin Zhen, Li Tang, Xue-Wei Xu, Li-Li Li, Dong-Zhi 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)
	370.	Further evidence for causation of ischiospinal dysostosis by a pathogenic variant in BMPER and expansion of the phenotype. [electronic resource] by Salian, Smrithi Nampoothiri, Sheela Shukla, Anju Girisha, Katta M Producer: 20190904 In: Congenital anomalies vol. 59 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	371.	Effects of the Y-chromosome and the dominant hemimelia mutation on the morphology of the mouse mandible. [electronic resource] by Suto, Jun-Ichi 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)
	372.	Morphological development of baculum and forelimb second-to-fourth digit ratio in mice. [electronic resource] by Fuse, Minami Sawada, Kazuhiko Producer: 20190904 In: Congenital anomalies vol. 59 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	373.	Early prenatal detection of Bardet-Biedl syndrome in a case with postaxial polydactyly and hyperechoic kidneys confirmed by next generation sequencing. [electronic resource] by Li, Qiao-Yi Huang, Lv-Ying Li, Dong-Zhi 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)
	374.	Ring chromosome 6 in a child with anterior segment dysgenesis and review of its overlap with other FOXC1 deletion phenotypes. [electronic resource] by Corona-Rivera, Jorge Román Corona-Rivera, Alfredo Zepeda-Romero, Luz Consuelo Rios-Flores, Izabel Maryalexandra Rivera-Vargas, Jehú Orozco-Vela, Mireya Santana-Bejarano, Uriel Francisco Torres-Anguiano, Elizabeth Pinto-Cardoso, Manuela David, Dezső Bobadilla-Morales, Lucina Producer: 20200124 In: Congenital anomalies vol. 59 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	375.	A female patient with X-linked Ohdo syndrome of the Maat-Kievit-Brunner phenotype caused by a novel variant of MED12. [electronic resource] by Murakami, Hiroaki Enomoto, Yumi Tsurusaki, Yoshinori Sugio, Yoshitsugu Kurosawa, Kenji Producer: 20210111 In: Congenital anomalies vol. 60 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	376.	THE 59TH ANNUAL MEETING OF THE JAPANESE TERATOLOGY SOCIETY THE 13TH WORLD CONGRESS OF THE INTERNATIONAL CLEFT LIP AND PALATE FOUNDATION - CLEFT 2019. [electronic resource] Publication details: Congenital anomalies Nov 2019 In: Congenital anomalies vol. 59 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	377.	Carnitine palmitoyltransferase II deficiency in a prenatal case with polycystic kidney disease-like phenotype. [electronic resource] by He, Yi Li, Dong-Zhi Producer: 20210527 In: Congenital anomalies vol. 60 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	378.	Position of the cecum in the extraembryonic and abdominal coelom in the early fetal period. [electronic resource] by Nagata, Akari Hatta, Shinnosuke Imai, Hirohiko Yamada, Shigehito Takakuwa, Tetsuya Producer: 20210111 In: Congenital anomalies vol. 60 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	379.	Necessity to establish new risk assessment and risk communication for human fetal exposure to multiple endocrine disruptors in Japan. [electronic resource] by Todaka, Emiko Mori, Chisato Producer: 20030212 In: Congenital anomalies vol. 42 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	380.	Enrichment of fetal cells from maternal blood by magnetic activated cell sorting (MACS) with fetal cell specific antibodies: one-step versus two-step MACS. [electronic resource] by Zhao, Xaio Xi Ozaki, Yasuhiko Suzumori, Nobuhiro Sato, Tsuyoshi Suzumori, Kaoru Producer: 20030212 In: Congenital anomalies vol. 42 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)

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Your search returned 648 results.