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Development and the evolvability of human limbs
Young, Nathan M, Wagner, Günter P, Hallgrímsson, Benedikt
Published in Proceedings of the National Academy of Sciences - PNAS (23.02.2010)
Published in Proceedings of the National Academy of Sciences - PNAS (23.02.2010)
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Autosomal Dominant Hypoparathyroidism Caused by Germline Mutation in GNA11: Phenotypic and Molecular Characterization
Li, Dong, Opas, Evan E., Tuluc, Florin, Metzger, Daniel L., Hou, Cuiping, Hakonarson, Hakon, Levine, Michael A.
Published in The journal of clinical endocrinology and metabolism (01.09.2014)
Published in The journal of clinical endocrinology and metabolism (01.09.2014)
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Mechanisms of action of thyroid hormones in the skeleton
Wojcicka, Anna, Bassett, J.H. Duncan, Williams, Graham R.
Published in Biochimica et biophysica acta (01.07.2013)
Published in Biochimica et biophysica acta (01.07.2013)
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Transgene‐mediated skeletal phenotypic variation in zebrafish
Kimmel, Charles B., Wind, Alexander L., Oliva, Whitney, Ahlquist, Samuel D., Walker, Charline, Dowd, John, Blanco‐Sánchez, Bernardo, Titus, Tom A., Batzel, Peter, Talbot, Jared C., Postlethwait, John H., Nichols, James T.
Published in Journal of fish biology (01.04.2021)
Published in Journal of fish biology (01.04.2021)
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Mutations in FAM20C Are Associated with Lethal Osteosclerotic Bone Dysplasia (Raine Syndrome), Highlighting a Crucial Molecule in Bone Development
Simpson, M.A., Hsu, R., Keir, L.S., Hao, J., Sivapalan, G., Ernst, L.M., Zackai, E.H., Al-Gazali, L.I., Hulskamp, G., Kingston, H.M., Prescott, T.E., Ion, A., Patton, M.A., Murday, V., George, A., Crosby, A.H.
Published in American journal of human genetics (01.11.2007)
Published in American journal of human genetics (01.11.2007)
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Tall Stature without Growth Hormone: Four Male Patients with Aromatase Deficiency
Rochira, Vincenzo, Zirilli, Lucia, Maffei, Laura, Premrou, Valeria, Aranda, Claudio, Baldi, Matteo, Ghigo, Ezio, Aimaretti, Gianluca, Carani, Cesare, Lanfranco, Fabio
Published in The journal of clinical endocrinology and metabolism (01.04.2010)
Published in The journal of clinical endocrinology and metabolism (01.04.2010)
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The Phenotype of Short Stature Homeobox Gene (SHOX) Deficiency in Childhood: Contrasting Children with Leri-Weill Dyschondrosteosis and Turner Syndrome
Ross, Judith L., Kowal, Karen, Quigley, Charmian A., Blum, Werner F., Cutler, Gordon B., Crowe, Brenda, Hovanes, Karine, Elder, Frederick F., Zinn, Andrew R.
Published in The Journal of pediatrics (01.10.2005)
Published in The Journal of pediatrics (01.10.2005)
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A Genome‐Wide Linkage Scan for Quantitative Trait Loci Influencing the Craniofacial Complex in Humans (Homo sapiens sapiens)
Sherwood, Richard J., Duren, Dana L., Mahaney, Michael C., Blangero, John, Dyer, Thomas D., Cole, Shelley A., Czerwinski, Stefan A., Chumlea, WM. Cameron, Siervogel, Roger M., Choh, Audrey C., Nahhas, Ramzi W., Lee, Miryoung, Towne, Bradford
Published in Anatomical record (Hoboken, N.J. : 2007) (01.04.2011)
Published in Anatomical record (Hoboken, N.J. : 2007) (01.04.2011)
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A follow-up linkage study for bone size variation in an extended sample
Xu, Fu-Hua, Liu, Yong-Jun, Deng, Hongyi, Huang, Qing-Yang, Zhao, Lan-Juan, Shen, Hui, Liu, Yao-Zhong, Dvornyk, Volodymyr, Conway, Theresa, Li, Jin-Long, Davies, K.Michael, Recker, Robert R., Deng, Hong-Wen
Published in Bone (New York, N.Y.) (01.09.2004)
Published in Bone (New York, N.Y.) (01.09.2004)
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Immortalization and Characterization of Bone Marrow Stromal Fibroblasts from a Patient with a Loss of Function Mutation in the Estrogen Receptor‐α Gene
Dieudonné, S. C., Xu, T., Chou, J. Y., Kuznetsov, S. A., Satomura, K., Mankani, M., Fedarko, N. S., Smith, E. P., Robey, P. Gehron, Young, M. F.
Published in Journal of bone and mineral research (01.04.1998)
Published in Journal of bone and mineral research (01.04.1998)
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