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Table representation of search results timeline featuring number of search results per year.

Year Number of Results
1951 1
1953 1
1954 2
1955 2
1957 3
1958 1
1959 3
1960 6
1961 2
1962 6
1965 14
1966 39
1967 43
1968 32
1969 35
1970 57
1971 49
1972 47
1973 37
1974 68
1975 55
1976 53
1977 49
1978 54
1979 57
1980 59
1981 46
1982 66
1983 67
1984 55
1985 61
1986 74
1987 91
1988 81
1989 73
1990 58
1991 94
1992 96
1993 143
1994 91
1995 133
1996 149
1997 182
1998 179
1999 183
2000 188
2001 171
2002 164
2003 186
2004 198
2005 220
2006 255
2007 267
2008 273
2009 288
2010 333
2011 346
2012 414
2013 446
2014 515
2015 533
2016 485
2017 516
2018 526
2019 243
2020 5
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8,480 results
Results by year
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Page 1
Clinical genetics of craniosynostosis
Wilkie AOM, et al. Curr Opin Pediatr 2017 - Review. PMID 28914635 Free PMC article.
RECENT FINDINGS: Survey of a 13-year birth cohort of patients treated at a single craniofacial unit demonstrates that a genetic cause of craniosynostosis can be identified in one quarter of cases. ...
RECENT FINDINGS: Survey of a 13-year birth cohort of patients treated at a single craniofacial unit demonstrates that a genetic cause …
Craniofacial developmental abnormalities.
Elmslie FV and Reardon W. Curr Opin Neurol 1998 - Review. PMID 9551288
Major advances have been made in the elucidation of the molecular basis of a number of human dysmorphic syndromes involving abnormalities of craniofacial development. This will lead, in turn, to a greater understanding of the mechanisms that underlie normal craniofacial development....
Major advances have been made in the elucidation of the molecular basis of a number of human dysmorphic syndromes involving abnormalities of …
Summarizing craniofacial genetics and developmental biology (SCGDB).
Hall BK. Am J Med Genet A 2014 - Review. PMID 24482307
This overview article highlights active areas of research in craniofacial genetics and developmental biology as reflected in presentations given at the 34th annual meeting of the Society of Craniofacial Genetics and Developmental Biology (SCGDB) in Montreal, Quebec on October 11, 2011. ...After discussing the basis on which craniofacial defects/syndromes are classified and investigated, I address the multi-gene basis of craniofacial syndromes with an examination of the roles of Sox9 and FGF receptors in normal and abnormal craniofacial development. ...
This overview article highlights active areas of research in craniofacial genetics and developmental biology as reflected in presenta …
The society for craniofacial genetics and developmental biology 39th annual meeting.
Fish JL, et al. Am J Med Genet A 2017. PMID 28168819
The Society for Craniofacial Genetics and Developmental Biology (SCGDB) aims to promote education, research, and communication, about normal and abnormal development of the tissues and organs of the head. Membership of the SCGDB is broad and diverse-including clinicians, orthodontists, scientists, and academics-but with all members sharing an interest in craniofacial biology. ...
The Society for Craniofacial Genetics and Developmental Biology (SCGDB) aims to promote education, research, and communication, about …
Introduction
Kruszka P, et al. Am J Med Genet C Semin Med Genet 2018. PMID 30182443
The Genetics of Primary Microcephaly
Jayaraman D, et al. Annu Rev Genomics Hum Genet 2018 - Review. PMID 29799801
Bone mineralization-dependent craniosynostosis and craniofacial shape abnormalities in the mouse model of infantile hypophosphatasia.
Durussel J, et al. Dev Dyn 2016. PMID 26605996 Free article.
Infants and mice with HPP can also develop craniosynostosis and craniofacial shape abnormalities, although the mechanism by which TNAP deficiency causes these craniofacial defects is not yet known. ...Here, we performed a comprehensive analysis of craniosynostosis and craniofacial shape variation in the Alpl(-/-) mouse model of murine HPP as an initial step toward better understanding penetrance of the HPP craniofacial phenotype. ...
Infants and mice with HPP can also develop craniosynostosis and craniofacial shape abnormalities, although the mechanism by which TNA …
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