Skip to main page content
Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation

Search Page

MyNCBI Filters
Results by year

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

Year Number of Results
1945 10
1946 48
1947 78
1948 56
1949 46
1950 101
1951 158
1952 148
1953 131
1954 145
1955 164
1956 153
1957 199
1958 177
1959 184
1960 205
1961 270
1962 291
1963 462
1964 635
1965 470
1966 393
1967 626
1968 886
1969 1006
1970 1028
1971 1277
1972 1209
1973 1207
1974 1323
1975 1206
1976 1203
1977 1226
1978 1224
1979 1215
1980 1191
1981 1308
1982 1274
1983 1404
1984 1490
1985 1508
1986 1420
1987 1652
1988 1583
1989 1660
1990 1871
1991 1828
1992 1951
1993 2254
1994 2113
1995 2160
1996 2314
1997 2362
1998 2327
1999 2389
2000 2577
2001 2648
2002 2459
2003 2614
2004 2740
2005 3018
2006 3145
2007 3242
2008 3399
2009 3443
2010 3940
2011 4020
2012 4015
2013 4258
2014 4214
2015 4025
2016 3844
2017 3589
2018 3503
2019 1727
2020 28
Text availability
Article attribute
Article type
Publication date

Search Results

114,869 results
Results by year
Filters applied: . Clear all
Page 1
Consequences of chromsome18q deletions
Cody JD, et al. Am J Med Genet C Semin Med Genet 2015 - Review. PMID 26235940
[Kabuki syndrome: Update and review]
Arnaud M, et al. Arch Pediatr 2015 - Review. PMID 25934606 French.
Syndromes associated with holoprosencephaly
Kruszka P and Muenke M. Am J Med Genet C Semin Med Genet 2018. PMID 29770994 Free PMC article.
Neuroimaging findings in Pallister-Killian syndrome
Barkovich EJ, et al. Neuroradiol J 2018 - Review. PMID 29260614 Free PMC article.
We present detailed neuroimaging findings from a child with PKS and thoroughly review previously reported structural brain abnormalities in this patient population. MRI abnormalities common to PKS include cerebral volume loss, malformations of cortical development, corpus callosum dysgenesis, white matter disease, and craniofacial malformations. ...
We present detailed neuroimaging findings from a child with PKS and thoroughly review previously reported structural brain abnormalities
Associated anomalies in cases with anorectal anomalies
Stoll C, et al. Am J Med Genet A 2018. PMID 30548801
There were 7 (3.3%) cases with chromosomal abnormalities, and 31 (15.3%) nonchromosomal recognized dysmorphic conditions, including 17 cases with Vertebral defects, Anal atresia, Cardiac septal defects, esophageal atresia or TracheoEsophageal fistula, Renal anomalies and radial Limb defects association. ...
There were 7 (3.3%) cases with chromosomal abnormalities, and 31 (15.3%) nonchromosomal recognized dysmorphic conditions, including 1 …
Extracephalic manifestations of nonchromosomal, nonsyndromic holoprosencephaly
Martinez AF, et al. Am J Med Genet C Semin Med Genet 2018 - Review. PMID 29761634 Free PMC article.
Likely, a complex network of interacting genetic variants and environmental factors is responsible for these systemic abnormalities that deviate from the usual brain and craniofacial findings in NCNS-HPE. ...
Likely, a complex network of interacting genetic variants and environmental factors is responsible for these systemic abnormalities t …
A review of 18p deletions
Hasi-Zogaj M, et al. Am J Med Genet C Semin Med Genet 2015. PMID 26250845
Proboscis lateralis
Martin S, et al. Childs Nerv Syst 2013 - Review. PMID 23354442
INTRODUCTION: Proboscis lateralis is a rare congenitally acquired facial abnormality characterized by a soft-tissue tube- or trunk-like appendage projecting from the surface of the face, most frequently rooted in the medial canthal region. ...
INTRODUCTION: Proboscis lateralis is a rare congenitally acquired facial abnormality characterized by a soft-tissue tube- or trunk-li …
114,869 results
Jump to page
Feedback