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- 2010051327 contributor B11798268.
- 2010051327 created "2011.".
- 2010051327 date "2011".
- 2010051327 date "2011.".
- 2010051327 dateCopyrighted "2011.".
- 2010051327 description "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) --".
- 2010051327 description "Includes bibliographical references and indexes.".
- 2010051327 description "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).".
- 2010051327 extent "x, 249 pages :".
- 2010051327 identifier "3805595948 (hard cover : alk. paper)".
- 2010051327 identifier "3805595956 (e-ISBN)".
- 2010051327 identifier "9783805595940 (hard cover : alk. paper)".
- 2010051327 identifier "9783805595957 (e-ISBN)".
- 2010051327 isPartOf "Monographs in human genetics ; v. 19. 0077-0876".
- 2010051327 isPartOf "Monographs in human genetics, 0077-0876 ; vol. 19".
- 2010051327 issued "2011".
- 2010051327 issued "2011.".
- 2010051327 language "eng".
- 2010051327 publisher "Basel : Karger,".
- 2010051327 subject "Craniosynostoses diagnosis.".
- 2010051327 subject "Craniosynostoses genetics.".
- 2010051327 subject "Craniosynostoses therapy.".
- 2010051327 subject "Craniosynostoses.".
- 2010051327 subject "RJ482.C73 C69 2011".
- 2010051327 tableOfContents "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) --".
- 2010051327 tableOfContents "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).".
- 2010051327 title "Craniosynostoses : molecular genetics, principles of diagnosis and treatment / Volume Editors, Maximilian Muenke, Bethesda, Md, Wolfram Kress, Würzburg, Hartmut Collmann, Würzburg, Benjamin Solomon, Bethesda, Md.".
- 2010051327 type "text".