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	1.	Extended clinical phenotype, endocrine investigations and functional studies of a loss-of-function mutation A150V in the thyroid hormone specific transporter MCT8. [electronic resource] by Biebermann, Heike Ambrugger, Petra Tarnow, Patrick von Moers, Arpad Schweizer, Ulrich Grueters, Annette Producer: 20051104 In: European journal of endocrinology vol. 153 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	2.	Low prevalence of Gs alpha mutations in śomatotroph adenomas of children and adolescents. [electronic resource] by Metzler, Markus Luedecke, Dieter K Saeger, Wolfgang Grueters, Annette Haberl, Hannes Kiess, Wieland Repp, Reinald Rascher, Wolfgang Doetsch, Joerg Producer: 20060525 In: Cancer genetics and cytogenetics vol. 166 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	3.	An Alu element-associated hypermethylation variant of the POMC gene is associated with childhood obesity. [electronic resource] by Kuehnen, Peter Mischke, Mona Wiegand, Susanna Sers, Christine Horsthemke, Bernhard Lau, Susanne Keil, Thomas Lee, Young-Ae Grueters, Annette Krude, Heiko Producer: 20120904 In: PLoS genetics vol. 8 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	4.	Increased transactivation associated with SOX3 polyalanine tract deletion in a patient with hypopituitarism. [electronic resource] by Alatzoglou, Kyriaki S Kelberman, Daniel Cowell, Christopher T Palmer, Rodger Arnhold, Ivo J P Melo, Maria E Schnabel, Dirk Grueters, Annette Dattani, Mehul T Producer: 20110614 In: The Journal of clinical endocrinology and metabolism vol. 96 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	5.	Novel mutations in LHX3 are associated with hypopituitarism and sensorineural hearing loss. [electronic resource] by Rajab, Anna Kelberman, Daniel de Castro, Sandra C P Biebermann, Heike Shaikh, Hala Pearce, Kerra Hall, Catherine M Shaikh, Guftar Gerrelli, Dianne Grueters, Annette Krude, Heiko Dattani, Mehul T Producer: 20080807 In: Human molecular genetics vol. 17 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	6.	Association between mutations in a thyroid hormone transporter and severe X-linked psychomotor retardation. [electronic resource] by Friesema, Edith C H Grueters, Annette Biebermann, Heike Krude, Heiko von Moers, Arpad Reeser, Maarten Barrett, Timothy G Mancilla, Edna E Svensson, Johan Kester, Monique H A Kuiper, George G J M Balkassmi, Sahila Uitterlinden, André G Koehrle, Josef Rodien, Patrice Halestrap, Andrew P Visser, Theo J Producer: 20041122 In: Lancet (London, England) vol. 364 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)