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

Year Number of Results
1922 1
1928 1
1931 1
1932 2
1933 4
1935 4
1936 3
1937 1
1939 1
1941 1
1943 1
1948 1
1949 1
1956 2
1963 1
1970 1
1987 1
1988 1
1989 2
1990 1
1991 1
1992 1
1993 3
1994 3
1995 2
1996 5
1997 5
1998 5
1999 6
2000 8
2001 8
2002 13
2003 12
2004 3
2005 2
2006 9
2007 9
2008 7
2009 5
2010 12
2011 8
2012 7
2013 7
2014 5
2015 6
2016 7
2017 7
2018 8
2019 9
2020 4
Text availability
Article attribute
Article type
Publication date

Similar Articles for PMID: 12372734

210 results
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Page 1
Novel HESX1 mutations associated with a life-threatening neonatal phenotype, pituitary aplasia, but normally located posterior pituitary and no optic nerve abnormalities.
Sobrier ML, Maghnie M, Vié-Luton MP, Secco A, di Iorgi N, Lorini R, Amselem S. Sobrier ML, et al. J Clin Endocrinol Metab. 2006 Nov;91(11):4528-36. doi: 10.1210/jc.2006-0426. Epub 2006 Aug 29. J Clin Endocrinol Metab. 2006. PMID: 16940453
Septo-optic dysplasia complex: a heterogeneous malformation syndrome.
Polizzi A, Pavone P, Iannetti P, Manfré L, Ruggieri M. Polizzi A, et al. Pediatr Neurol. 2006 Jan;34(1):66-71. doi: 10.1016/j.pediatrneurol.2005.07.004. Pediatr Neurol. 2006. PMID: 16376284
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