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GREB1L gene

Known as: growth regulation by estrogen in breast cancer-like, C18orf6, GREB1L 
 
National Institutes of Health

Papers overview

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2020
2020
Congenital uterine anomalies (CUA) may have major impacts on the health and social well-being of affected individuals. Their… Expand
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2019
2019
The aetiology of Mayer-Rokitansky-Küster-Hauser (MRKH) syndrome, characterized by uterovaginal agenesis in 46,XX women, remains… Expand
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2019
2019
Gastric adenocarcinoma is an important death-related cancer. To find factors related to survival and prognosis, and thus improve… Expand
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2018
2018
PurposeFetal anomalies represent a poorly studied group of developmental disorders. Our objective was to assess the impact of… Expand
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2018
2018
Congenital inner ear malformations affecting both the osseous and membranous labyrinth can have a devastating impact on hearing… Expand
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2018
2018
Identification of fetal kidney anomalies invites questions about underlying causes and recurrence risk in future pregnancies. We… Expand
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2018
2018
BackgroundDisparity in the timing of biological events occurs across a variety of systems, yet the understanding of genetic basis… Expand
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2017
2017
Renal agenesis and hypodysplasia (RHD) are major causes of pediatric chronic kidney disease and are highly genetically… Expand
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2017
2017
Congenital anomalies of the kidney and urinary tract (CAKUT) constitute a major cause of chronic kidney disease in children and… Expand
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2017
2017
Renal agenesis is a devastating birth defect, and although genes encoding retinoic acid signaling components have been shown to… Expand
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