Source updated
Genes & inheritance
conf 80%
Updated: Clinical characteristics and etiologies of hypomagnesemia in children: a single-center retrospective cohort study.
pubmed changed: +376/-0 sentences since the previous capture.
New insights
Everything the analysis engine concluded from the corpus: new publications, sources that changed, gene–trait links, reported figures, care recommendations and contradicting evidence. Each card shows how many independent sources support it and links to the exact sentence.
Source updated
kidney and urinary tract
conf 80%
Updated: A Case of Amyotrophic Lateral Sclerosis With Coexisting Maturity-onset Diabetes of the Young Type 5.
pubmed changed: +0/-298 sentences since the previous capture.
Source updated
kidney and urinary tract
conf 80%
Updated: 17q12 Recurrent Deletion Syndrome in Childhood
pmc changed: +3/-90 sentences since the previous capture.
Source updated
kidney and urinary tract
conf 80%
Updated: Atypical presentation of HNF1β gene mutation mimicking type 2 diabetes: Case report and literature review
pmc changed: +4/-28 sentences since the previous capture.
Source updated
How it is diagnosed
conf 80%
Updated: Clinical and Genetic Significance of Chromosomal Microarray Screening of Asymptomatic Newborns
pmc changed: +17/-42 sentences since the previous capture.
Source updated
kidney and urinary tract
conf 80%
Updated: Genetics of CAKUT
pmc changed: +1/-59 sentences since the previous capture.
Source updated
kidney and urinary tract
conf 80%
Updated: Chromosome 17q12 deletion, including HNF1B presenting with recurrent severe cholestasis and profound hypomagnesemia duri
pubmed changed: +3/-8 sentences since the previous capture.
Source updated
kidney and urinary tract
conf 80%
Updated: 17q12 deletion syndrome presenting with chronic pancreatitis: a case report.
pubmed changed: +2/-8 sentences since the previous capture.
Source updated
How it is diagnosed
conf 80%
Updated: Genetic evaluation and pregnancy outcome of fetuses with digestive system malformations: an eight-year single-center ret
pubmed changed: +3/-7 sentences since the previous capture.
Source updated
Genes & inheritance
conf 80%
Updated: A familial case report of 17q12 recurrent deletion syndrome: clinical and molecular characterization.
pubmed changed: +2/-13 sentences since the previous capture.
Source updated
kidney and urinary tract
conf 80%
Updated: HNF1B -related disease: developmental origins, molecular mechanisms, and multisystem clinical challenges.
pubmed changed: +3/-3 sentences since the previous capture.