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	1.	Not all amino acid substitutions of the common cluster E6 mutation in CYP21 cause congenital adrenal hyperplasia. [electronic resource] by Robins, Tiina Barbaro, Michela Lajic, Svetlana Wedell, Anna Producer: 20050531 In: The Journal of clinical endocrinology and metabolism vol. 90 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	2.	Molecular model of human CYP21 based on mammalian CYP2C5: structural features correlate with clinical severity of mutations causing congenital adrenal hyperplasia. [electronic resource] by Robins, Tiina Carlsson, Jonas Sunnerhagen, Maria Wedell, Anna Persson, Bengt Producer: 20070212 In: Molecular endocrinology (Baltimore, Md.) vol. 20 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	3.	Characterization of novel missense mutations in CYP21 causing congenital adrenal hyperplasia. [electronic resource] by Robins, Tiina Bellanne-Chantelot, Christine Barbaro, Michela Cabrol, Sylvie Wedell, Anna Lajic, Svetlana Producer: 20080124 In: Journal of molecular medicine (Berlin, Germany) vol. 85 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	4.	Novel mutations in CYP21 detected in individuals with hyperandrogenism. [electronic resource] by Lajić, Svetlana Clauin, Séverine Robins, Tiina Vexiau, Patrick Blanché, Hélène Bellanne-Chantelot, Christine Wedell, Anna Producer: 20020703 In: The Journal of clinical endocrinology and metabolism vol. 87 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	5.	Three novel CYP21A2 mutations and their protein modelling in patients with classical 21-hydroxylase deficiency from northeastern Iran. [electronic resource] by Baradaran-Heravi, Alireza Vakili, Rahim Robins, Tiina Carlsson, Jonas Ghaemi, Nosrat A'rabi, Azadeh Abbaszadegan, Mohammad Reza Producer: 20111027 In: Clinical endocrinology vol. 67 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	6.	Progranulin mutation causes frontotemporal dementia in the Swedish Karolinska family. [electronic resource] by Chiang, Huei-Hsin Rosvall, Lina Brohede, Jesper Axelman, Karin Björk, Behnosh F Nennesmo, Inger Robins, Tiina Graff, Caroline Producer: 20081210 In: Alzheimer's & dementia : the journal of the Alzheimer's Association vol. 4 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)