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A Novel Synonymous Variant in the AVP Gene Associated with Autosomal Dominant Familial Neurohypophyseal Diabetes Insipidus Causes Partial RNA Missplicing.
Neuroendocrinology. 2018;107(2):167-180. doi: 10.1159/000491579. Epub 2018 Jun 27.
Neuroendocrinology. 2018.
PMID: 29949799
A novel variant in the SLC12A1 gene in two families with antenatal Bartter syndrome.
Breinbjerg A, Siggaard Rittig C, Gregersen N, Rittig S, Hvarregaard Christensen J.
Breinbjerg A, et al. Among authors: siggaard rittig c.
Acta Paediatr. 2017 Jan;106(1):161-167. doi: 10.1111/apa.13635.
Acta Paediatr. 2017.
PMID: 27748541
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Bladder and bowel dysfunction and the resolution of urinary incontinence with successful management of bowel symptoms in children.
Borch L, Hagstroem S, Bower WF, Siggaard Rittig C, Rittig S.
Borch L, et al. Among authors: siggaard rittig c.
Acta Paediatr. 2013 May;102(5):e215-20. doi: 10.1111/apa.12158. Epub 2013 Feb 11.
Acta Paediatr. 2013.
PMID: 23368903
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