Results
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3761.
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3762.
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3763.
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3764.
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Impaired proteostasis contributes to renal tubular dysgenesis. [electronic resource] by
- de Oliveira, Rita Machado
- Marijanovic, Zrinka
- Carvalho, Filipe
- Miltényi, Gabriel Miltenberger
- Matos, Joana Estevão
- Tenreiro, Sandra
- Oliveira, Sónia
- Enguita, Francisco Javier
- Stone, Rosário
- Outeiro, Tiago Fleming
Producer: 20111021
In:
PloS one vol. 6
Availability: No items available.
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3765.
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3766.
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Integrative Analyses of Uterine Transcriptome and MicroRNAome Reveal Compromised LIF-STAT3 Signaling and Progesterone Response in the Endometrium of Patients with Recurrent/Repeated Implantation Failure (RIF). [electronic resource] by
- Choi, Youngsok
- Kim, Hye-Ryun
- Lim, Eun Jin
- Park, Miseon
- Yoon, Jung Ah
- Kim, Yeon Sun
- Kim, Eun-Kyung
- Shin, Ji-Eun
- Kim, Ji Hyang
- Kwon, Hwang
- Song, Haengseok
- Choi, Dong-Hee
Producer: 20170724
In:
PloS one vol. 11
Availability: No items available.
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3767.
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3768.
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3769.
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3770.
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3771.
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3772.
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3773.
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3774.
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3775.
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3776.
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Pure laparoscopic and robot-assisted laparoscopic reconstructive surgery in congenital megaureter: a single institution experience. [electronic resource] by
- Fu, Weijun
- Zhang, Xu
- Zhang, Xiaoyi
- Zhang, Peng
- Gao, Jiangping
- Dong, Jun
- Chen, Guangfu
- Xu, Axiang
- Ma, Xin
- Li, Hongzhao
- Shi, Lixin
Producer: 20151214
In:
PloS one vol. 9
Availability: No items available.
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3777.
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3778.
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Fraser syndrome: features suggestive of prenatal diagnosis in a review of 38 cases. [electronic resource] by
- Tessier, Aude
- Sarreau, Mélie
- Pelluard, Fanny
- André, Gwenaelle
- Blesson, Sophie
- Bucourt, Martine
- Dechelotte, Pierre
- Faivre, Laurence
- Frébourg, Thierry
- Goldenberg, Alice
- Goua, Valérie
- Jeanne-Pasquier, Corinne
- Guimiot, Fabien
- Laquerriere, Annie
- Laurent, Nicole
- Lefebvre, Mathilde
- Loget, Philippe
- Maréchaud, Martine
- Mechler, Charlotte
- Perez, Marie-Josée
- Sabourin, Jean Christophe
- Verloes, Alain
- Patrier, Sophie
- Guerrot, Anne-Marie
Producer: 20170726
In:
Prenatal diagnosis vol. 36
Availability: No items available.
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3779.
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3780.
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DDX3X mutations in two girls with a phenotype overlapping Toriello-Carey syndrome. [electronic resource] by
- Dikow, Nicola
- Granzow, Martin
- Graul-Neumann, Luitgard M
- Karch, Stephanie
- Hinderhofer, Katrin
- Paramasivam, Nagarajan
- Behl, Laura-Jane
- Kaufmann, Lilian
- Fischer, Christine
- Evers, Christina
- Schlesner, Matthias
- Eils, Roland
- Borck, Guntram
- Zweier, Christiane
- Bartram, Claus R
- Carey, John C
- Moog, Ute
Producer: 20170508
In:
American journal of medical genetics. Part A vol. 173
Availability: No items available.
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