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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 554
2019 526
2020 614
2021 620
2022 723
2023 585
2024 524
2025 296

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11,557 results

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Page 1
Genetics of craniofacial malformations.
Schmetz A, Amiel J, Wieczorek D. Schmetz A, et al. Semin Fetal Neonatal Med. 2021 Dec;26(6):101290. doi: 10.1016/j.siny.2021.101290. Epub 2021 Sep 17. Semin Fetal Neonatal Med. 2021. PMID: 34561177 Review.
Clinical overview on RASopathies.
Zenker M. Zenker M. Am J Med Genet C Semin Med Genet. 2022 Dec;190(4):414-424. doi: 10.1002/ajmg.c.32015. Epub 2022 Nov 25. Am J Med Genet C Semin Med Genet. 2022. PMID: 36428239 Review.
POLR1A variants underlie phenotypic heterogeneity in craniofacial, neural, and cardiac anomalies.
Smallwood K, Watt KEN, Ide S, Baltrunaite K, Brunswick C, Inskeep K, Capannari C, Adam MP, Begtrup A, Bertola DR, Demmer L, Demo E, Devinsky O, Gallagher ER, Guillen Sacoto MJ, Jech R, Keren B, Kussmann J, Ladda R, Lansdon LA, Lunke S, Mardy A, McWalters K, Person R, Raiti L, Saitoh N, Saunders CJ, Schnur R, Skorvanek M, Sell SL, Slavotinek A, Sullivan BR, Stark Z, Symonds JD, Wenger T, Weber S, Whalen S, White SM, Winkelmann J, Zech M, Zeidler S, Maeshima K, Stottmann RW, Trainor PA, Weaver KN. Smallwood K, et al. Am J Hum Genet. 2023 May 4;110(5):809-825. doi: 10.1016/j.ajhg.2023.03.014. Epub 2023 Apr 18. Am J Hum Genet. 2023. PMID: 37075751 Free PMC article.
Craniofacial developmental abnormalities.
Elmslie FV, Reardon W. Elmslie FV, et al. Curr Opin Neurol. 1998 Apr;11(2):103-8. doi: 10.1097/00019052-199804000-00004. Curr Opin Neurol. 1998. PMID: 9551288 Review.
Diversity and dysmorphology.
Kruszka P, Tekendo-Ngongang C, Muenke M. Kruszka P, et al. Curr Opin Pediatr. 2019 Dec;31(6):702-707. doi: 10.1097/MOP.0000000000000816. Curr Opin Pediatr. 2019. PMID: 31693576 Review.
A multi-stem cell basis for craniosynostosis and calvarial mineralization.
Bok S, Yallowitz AR, Sun J, McCormick J, Cung M, Hu L, Lalani S, Li Z, Sosa BR, Baumgartner T, Byrne P, Zhang T, Morse KW, Mohamed FF, Ge C, Franceschi RT, Cowling RT, Greenberg BH, Pisapia DJ, Imahiyerobo TA, Lakhani S, Ross ME, Hoffman CE, Debnath S, Greenblatt MB. Bok S, et al. Nature. 2023 Sep;621(7980):804-812. doi: 10.1038/s41586-023-06526-2. Epub 2023 Sep 20. Nature. 2023. PMID: 37730988 Free PMC article.
Congenital microcephaly.
Alcantara D, O'Driscoll M. Alcantara D, et al. Am J Med Genet C Semin Med Genet. 2014 Jun;166C(2):124-39. doi: 10.1002/ajmg.c.31397. Epub 2014 May 9. Am J Med Genet C Semin Med Genet. 2014. PMID: 24816482 Review.
Jackson-Weiss syndrome.
Cohen MM Jr. Cohen MM Jr. Am J Med Genet. 2001 May 15;100(4):325-9. doi: 10.1002/ajmg.1271. Am J Med Genet. 2001. PMID: 11343324 No abstract available.
Molecular genetics and craniofacial surgery.
Mulliken JB, Warman ML. Mulliken JB, et al. Plast Reconstr Surg. 1996 Mar;97(3):666-75. doi: 10.1097/00006534-199603000-00030. Plast Reconstr Surg. 1996. PMID: 8596804 Review. No abstract available.
11,557 results
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