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	1.	New Genetic Forms of Childhood-Onset Primary Osteoporosis. [electronic resource] by Kämpe, Anders J Mäkitie, Riikka E Mäkitie, Outi Producer: 20161005 In: Hormone research in paediatrics vol. 84 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	2.	Recent Discoveries in Monogenic Disorders of Childhood Bone Fragility. [electronic resource] by Mäkitie, Riikka E Kämpe, Anders J Taylan, Fulya Mäkitie, Outi Producer: 20180507 In: Current osteoporosis reports vol. 15 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	3.	New Insights Into Monogenic Causes of Osteoporosis. [electronic resource] by Mäkitie, Riikka E Costantini, Alice Kämpe, Anders Alm, Jessica J Mäkitie, Outi Publication details: Frontiers in endocrinology 2019 In: Frontiers in endocrinology vol. 10 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	4.	Biomarkers in WNT1 and PLS3 Osteoporosis: Altered Concentrations of DKK1 and FGF23. [electronic resource] by Mäkitie, Riikka E Kämpe, Anders Costantini, Alice Alm, Jessica J Magnusson, Per Mäkitie, Outi Producer: 20210728 In: Journal of bone and mineral research : the official journal of the American Society for Bone and Mineral Research vol. 35 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	5.	Autosomal Recessive Osteogenesis Imperfecta Caused by a Novel Homozygous COL1A2 Mutation. [electronic resource] by Costantini, Alice Tournis, Symeon Kämpe, Anders Ul Ain, Noor Taylan, Fulya Doulgeraki, Artemis Mäkitie, Outi Producer: 20190909 In: Calcified tissue international vol. 103 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	6.	A novel frameshift deletion in PLS3 causing severe primary osteoporosis. [electronic resource] by Costantini, Alice Krallis, Panagiotis Ν Kämpe, Anders Karavitakis, Emmanouil M Taylan, Fulya Mäkitie, Outi Doulgeraki, Artemis Producer: 20181106 In: Journal of human genetics vol. 63 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	7.	Rare Variants in Genes Linked to Appetite Control and Hypothalamic Development in Early-Onset Severe Obesity. [electronic resource] by Loid, Petra Mustila, Taina Mäkitie, Riikka E Viljakainen, Heli Kämpe, Anders Tossavainen, Päivi Lipsanen-Nyman, Marita Pekkinen, Minna Mäkitie, Outi Producer: 20210302 In: Frontiers in endocrinology vol. 11 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	8.	Genetic variation in GC and CYP2R1 affects 25-hydroxyvitamin D concentration and skeletal parameters: A genome-wide association study in 24-month-old Finnish children. [electronic resource] by Kämpe, Anders Enlund-Cerullo, Maria Valkama, Saara Holmlund-Suila, Elisa Rosendahl, Jenni Hauta-Alus, Helena Pekkinen, Minna Andersson, Sture Mäkitie, Outi Producer: 20200303 In: PLoS genetics vol. 15 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	9.	Rare Copy Number Variants in Array-Based Comparative Genomic Hybridization in Early-Onset Skeletal Fragility. [electronic resource] by Costantini, Alice Skarp, Sini Kämpe, Anders Mäkitie, Riikka E Pettersson, Maria Männikkö, Minna Jiao, Hong Taylan, Fulya Lindstrand, Anna Mäkitie, Outi Publication details: Frontiers in endocrinology 2018 In: Frontiers in endocrinology vol. 9 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	10.	Increased Burden of Common Risk Alleles in Children With a Significant Fracture History. [electronic resource] by Manousaki, Despoina Kämpe, Anders Forgetta, Vincenzo Makitie, Riikka E Bardai, Ghalib Belisle, Alexandre Li, Rui Andersson, Sture Makitie, Outi Rauch, Frank Richards, J Brent Producer: 20210728 In: Journal of bone and mineral research : the official journal of the American Society for Bone and Mineral Research vol. 35 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	11.	Spondyloocular Syndrome: Novel Mutations in XYLT2 Gene and Expansion of the Phenotypic Spectrum. [electronic resource] by Taylan, Fulya Costantini, Alice Coles, Nicole Pekkinen, Minna Héon, Elise Şıklar, Zeynep Berberoğlu, Merih Kämpe, Anders Kıykım, Ertuğrul Grigelioniene, Giedre Tüysüz, Beyhan Mäkitie, Outi Producer: 20171218 In: Journal of bone and mineral research : the official journal of the American Society for Bone and Mineral Research vol. 31 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	12.	CRTAP variants in early-onset osteoporosis and recurrent fractures. [electronic resource] by Costantini, Alice Vuorimies, Ilkka Mäkitie, Riikka Mäyränpää, Mervi K Becker, Jutta Pekkinen, Minna Valta, Helena Netzer, Christian Kämpe, Anders Taylan, Fulya Jiao, Hong Mäkitie, Outi Producer: 20171201 In: American journal of medical genetics. Part A vol. 173 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	13.	PLS3 Deletions Lead to Severe Spinal Osteoporosis and Disturbed Bone Matrix Mineralization. [electronic resource] by Kämpe, Anders J Costantini, Alice Levy-Shraga, Yael Zeitlin, Leonid Roschger, Paul Taylan, Fulya Lindstrand, Anna Paschalis, Eleftherios P Gamsjaeger, Sonja Raas-Rothschild, Annick Hövel, Matthias Jiao, Hong Klaushofer, Klaus Grasemann, Corinna Mäkitie, Outi Producer: 20180723 In: Journal of bone and mineral research : the official journal of the American Society for Bone and Mineral Research vol. 32 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)