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  2. Details for: The male phenotype in osteopathia striata congenita with cranial sclerosis.
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The male phenotype in osteopathia striata congenita with cranial sclerosis. [electronic resource]

By:
  • Holman, Sarah K
Contributor(s):
  • Daniel, Phil
  • Jenkins, Zandra A
  • Herron, Rachel L
  • Morgan, Tim
  • Savarirayan, Ravi
  • Chow, C W
  • Bohring, Axel
  • Mosel, Annette
  • Lacombe, Didier
  • Steiner, Bernhard
  • Schmitt-Mechelke, Thomas
  • Schroter, Barbara
  • Raas-Rothschild, Annick
  • Miñaur, Sixto Garcia
  • Porteous, Mary
  • Parker, Michael
  • Quarrell, Oliver
  • Tapon, Dagmar
  • Cormier-Daire, Valérie
  • Mansour, Sahar
  • Nash, Ruth
  • Bindoff, Laurence A
  • Fiskerstrand, Torunn
  • Robertson, Stephen P
Producer: 20120118Description: 2397-408 p. digitalISSN:
  • 1552-4833
Subject(s):
  • Adaptor Proteins, Signal Transducing -- genetics
  • Bone and Bones -- pathology
  • DNA Mutational Analysis
  • DNA Primers -- genetics
  • Female
  • Genetic Diseases, X-Linked -- genetics
  • Humans
  • Luciferases
  • Male
  • Megalencephaly -- pathology
  • Osteosclerosis -- genetics
  • Phenotype
  • Tumor Suppressor Proteins -- genetics
Online resources:
  • Available from publisher's website
In: American journal of medical genetics. Part A vol. 155A
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Publication Type: Journal Article; Research Support, Non-U.S. Gov't

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The male phenotype in osteopathia striata congenita with cranial sclerosis.

APA

Holman S. K., Daniel P., Jenkins Z. A., Herron R. L., Morgan T., Savarirayan R., Chow C. W., Bohring A., Mosel A., Lacombe D., Steiner B., Schmitt-Mechelke T., Schroter B., Raas-Rothschild A., Miñaur S. G., Porteous M., Parker M., Quarrell O., Tapon D., Cormier-Daire V., Mansour S., Nash R., Bindoff L. A., Fiskerstrand T. & Robertson S. P. (20120118). The male phenotype in osteopathia striata congenita with cranial sclerosis. : American journal of medical genetics. Part A.

Chicago

Holman Sarah K, Daniel Phil, Jenkins Zandra A, Herron Rachel L, Morgan Tim, Savarirayan Ravi, Chow C W, Bohring Axel, Mosel Annette, Lacombe Didier, Steiner Bernhard, Schmitt-Mechelke Thomas, Schroter Barbara, Raas-Rothschild Annick, Miñaur Sixto Garcia, Porteous Mary, Parker Michael, Quarrell Oliver, Tapon Dagmar, Cormier-Daire Valérie, Mansour Sahar, Nash Ruth, Bindoff Laurence A, Fiskerstrand Torunn and Robertson Stephen P. 20120118. The male phenotype in osteopathia striata congenita with cranial sclerosis. : American journal of medical genetics. Part A.

Harvard

Holman S. K., Daniel P., Jenkins Z. A., Herron R. L., Morgan T., Savarirayan R., Chow C. W., Bohring A., Mosel A., Lacombe D., Steiner B., Schmitt-Mechelke T., Schroter B., Raas-Rothschild A., Miñaur S. G., Porteous M., Parker M., Quarrell O., Tapon D., Cormier-Daire V., Mansour S., Nash R., Bindoff L. A., Fiskerstrand T. and Robertson S. P. (20120118). The male phenotype in osteopathia striata congenita with cranial sclerosis. : American journal of medical genetics. Part A.

MLA

Holman Sarah K, Daniel Phil, Jenkins Zandra A, Herron Rachel L, Morgan Tim, Savarirayan Ravi, Chow C W, Bohring Axel, Mosel Annette, Lacombe Didier, Steiner Bernhard, Schmitt-Mechelke Thomas, Schroter Barbara, Raas-Rothschild Annick, Miñaur Sixto Garcia, Porteous Mary, Parker Michael, Quarrell Oliver, Tapon Dagmar, Cormier-Daire Valérie, Mansour Sahar, Nash Ruth, Bindoff Laurence A, Fiskerstrand Torunn and Robertson Stephen P. The male phenotype in osteopathia striata congenita with cranial sclerosis. : American journal of medical genetics. Part A. 20120118.

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