MARC Record from Library of Congress

LEADER: 03778cam a22004217a 4500
001 2010051327
003 DLC
005 20111026082902.0
008 101203s2011 sz b 001 0 eng c
010 $a 2010051327
016 7 $a101548942$2DNLM
020 $a9783805595940 (hard cover : alk. paper)
020 $a3805595948 (hard cover : alk. paper)
020 $a9783805595957 (e-ISBN)
020 $a3805595956 (e-ISBN)
035 $a(OCoLC)ocn692015445
040 $aDNLM/DLC$erda$cDLC$dNLM$dYDXCP$dOHX$dCDX$dCUS$dDLC
042 $apcc
050 00 $aRJ482.C73$bC69 2011
245 00 $aCraniosynostoses :$bmolecular genetics, principles of diagnosis and treatment /$cVolume Editors, Maximilian Muenke, Bethesda, Md, Wolfram Kress, Würzburg, Hartmut Collmann, Würzburg, Benjamin Solomon, Bethesda, Md.
260 $aBasel :$bKarger,$c2011.
300 $ax, 249 pages :$billustrations (some color) ;$c26 cm.
336 $atext$2rdacontent
337 $aunmediated$2rdamedia
338 $avolume$2rdacarrier
490 1 $aMonographs in human genetics,$x0077-0876 ;$vvol. 19
504 $aIncludes bibliographical references and indexes.
505 0 $aCraniosynostosis : 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) --
505 0 $aUncommon 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).
650 0 $aCraniosynostoses.
650 12 $aCraniosynostoses$xgenetics.
650 22 $aCraniosynostoses$xdiagnosis.
650 22 $aCraniosynostoses$xtherapy.
700 1 $aMuenke, Maximilian,$eeditor.
700 1 $aKress, Wolfram,$eeditor.
700 1 $aCollmann, Hartmut,$eeditor.
700 1 $aSolomon, Benjamin,$eeditor.
830 0 $aMonographs in human genetics ;$vv. 19.$x0077-0876