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	1.	Unique near-complete deletion of GLI2 in a patient with combined pituitary hormone deficiency and post-axial polydactyly. [electronic resource] by Elizabeth, Melitza S M Verkerk, Annemieke J M H Hokken-Koelega, Anita C S Verlouw, Joost A M Argente, Jesús Pfaeffle, Roland Visser, Theo J Peeters, Robin P De Graaff, Laura C G Producer: 20210316 In: Growth hormone & IGF research : official journal of the Growth Hormone Research Society and the International IGF Research Society vol. 50 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	2.	Whole-Exome Sequencing in Age-Related Macular Degeneration Identifies Rare Variants in COL8A1, a Component of Bruch's Membrane. [electronic resource] by Corominas, Jordi Colijn, Johanna M Geerlings, Maartje J Pauper, Marc Bakker, Bjorn Amin, Najaf Lores Motta, Laura Kersten, Eveline Garanto, Alejandro Verlouw, Joost A M van Rooij, Jeroen G J Kraaij, Robert de Jong, Paulus T V M Hofman, Albert Vingerling, Johannes R Schick, Tina Fauser, Sascha de Jong, Eiko K van Duijn, Cornelia M Hoyng, Carel B Klaver, Caroline C W den Hollander, Anneke I Producer: 20190905 In: Ophthalmology vol. 125 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)

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