Search Results - Hallermeier, K M

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  1. 1
    Inactivation of the luteinizing hormone/chorionic gonadotropin receptor by an insertional mutation in Leydig cell hypoplasia

    Inactivation of the luteinizing hormone/chorionic gonadotropin receptor by an insertional mutation in Leydig cell hypoplasia by Wu, S M, Hallermeier, K M, Laue, L, Brain, C, Berry, A C, Grant, D B, Griffin, J E, Wilson, J D, Cutler, Jr, G B, Chan, W Y

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    Genetic Heterogeneity of Adrenocorticotropin (ACTH) Resistance Syndromes: Identification of a Novel Mutation of the ACTH Receptor Gene in Hereditary Glucocorticoid Deficiency

    Genetic Heterogeneity of Adrenocorticotropin (ACTH) Resistance Syndromes: Identification of a Novel Mutation of the ACTH Receptor Gene in Hereditary Glucocorticoid Deficiency by Wu, Shao-Ming, Stratakis, Constantine A., Chan, Connie H.Y., Hallermeier, Karen M., Bourdony, Carlos J., Rennert, Owen M., Chan, Wai-Yee

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    Polymorphisms in the coding exons of the human luteinizing hormone receptor gene. Mutations in brief no. 124. Online

    Polymorphisms in the coding exons of the human luteinizing hormone receptor gene. Mutations in brief no. 124. Online by Wu, S M, Jose, M, Hallermeier, K, Rennert, O M, Chan, W Y

    Published in Human mutation
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