An edition of Craniosynostoses
(2011)
Craniosynostoses
molecular genetics, principles of diagnosis and treatment
by Maximilian Muenke, Wolfram Kress, Hartmut Collmann, and Benjamin Solomon
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Subjects
Craniosynostoses, Genetics, Therapy, Diagnosis, Skull, abnormalities| Edition | Availability |
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Craniosynostoses: molecular genetics, principles of diagnosis and treatment
2011, Karger
in English
3805595948 9783805595940
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Book Details
Table of Contents
Craniosynostosis : a historical overview / Solomon, B.D. (Bethesda, Md.); Collmann, H.; Kress, W. (Würzburg); Muenke, M. (Bethesda, Md.)
Discovery of MSX2 mutation in craniosynostosis : a retrospective view / Müller, U. (Giessen)
Regulation of calvarial bone growth by molecules involved in the craniosynostoses / Benson, M.D.; Opperman, L.A. (Dallas Tex.)
Signal transduction pathways and their impairment in syndromic craniosynostosis / Connerney, J.J. (Boston, Mass.); Spicer, D.B. (Scarborough, Me.)
The molecular bases for FGF receptor activation in craniosynostosis and dwarfism syndromes / Beenken, A.; Mohammadi, M. (New York, N.Y.)
Recurrent germline mutations in the FGFR2/3 genes, high mutation frequency, paternal skewing and age-dependence / Arnheim, N.; Calabrese, P. (Los Angeles, Calif.)
Apert, Crouzon, and Pfeiffer syndromes / Cohen Jr., M.M. (Halifax, N.S.)
Muenke syndrome / Solomon, B.D.; Muenke, M. (Bethesda, Md.)
Saethre-Chotzen syndrome : clinical and molecular genetic aspects / Kress, W.; Collmann, H. (Würzburg)
Craniofrontonasal syndrome : molecular genetics, EFNB1 mutations and the concept of cellular interference / Wieland, I. (Magdeburg)
Uncommon craniosynostosis syndromes : a review of thirteen conditions / Raam, M.S. (Bethesda, Md./Chevy Chase, Md.); Muenke, M. (Bethesda, Md.)
Metopic craniosynostosis syndrome due to mutations in GLI3 / McDonald-McGinn, D.M.; Feret, H.; Nah, H.-D.; Zackai, E.H. (Philadelphia, Pa.)
Craniosynostosis and chromosomal alterations / Passos-Bueno, M.R.; Fanganiello, R.D.; Jehee, F.S. (Sao Paulo)
Nonsyndromic craniosynostoses / Collmann, H. (Würzburg); Solomon, B.D. (Bethesda, Md.); Schweitzer, T.; Kress, W. (Würzburg); Muenke, M. (Bethesda, Md.)
Molecular genetic testing of patients with craniosynostosis / Hehr, U. (Regensburg)
Prenatal sonographic diagnosis of craniosynostosis / Schramm, T. (Munich)
Clinical approach to craniosynostosis / Gripp, K.W. (Wilmington, Del.)
Imaging studies and neurosurgical treatment / Collmann, H.; Schweitzer, T.; Bohm, H. (Würzburg)
Maxillofacial examination and treatment / Bohm, H.; Schweitzer, T.; Kübler, A. (Würzburg).
Edition Notes
Includes bibliographical references and indexes.
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| July 17, 2024 | Edited by ImportBot | import existing book |
| November 14, 2020 | Edited by MARC Bot | import existing book |
| October 27, 2011 | Edited by LC Bot | import new book |
| October 27, 2011 | Created by LC Bot | import new book |