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Clinical practice guidelines for the care of girls and women with Turner syndromeClaus Højbjerg Gravholt, Rebecca Knickmeyer, N.H. Andersen et al.|European Journal of Endocrinology|2024Cited by 181
A recurrent de novo <i>FAM111A</i> mutation causes kenny–caffey syndrome type 2Tsuyoshi Isojima, Sachiko Kitanaka, Koichiro Doi et al.|Journal of Bone and Mineral Research|2013Cited by 89
LMX1B mutation with residual transcriptional activity as a cause of isolated glomerulopathyTsuyoshi Isojima, Sachiko Kitanaka|Nephrology Dialysis Transplantation|2013Cited by 50