Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation

Search Page

Filters

My NCBI Filters

Results by year

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

Year Number of Results
1958 2
1959 3
1961 5
1962 6
1963 2
1964 2
1965 2
1966 2
1967 2
1968 2
1969 2
1970 5
1972 2
1973 3
1974 4
1975 2
1976 7
1977 3
1978 1
1979 2
1980 10
1981 3
1982 4
1983 6
1984 3
1985 2
1986 6
1987 3
1988 2
1989 2
1993 1
1995 1
1997 2
1998 5
1999 1
2001 1
2002 1
2003 1
2004 1
2005 1
2006 1
2007 1
2013 1
2014 1
2016 1
2017 1
2023 0

Text availability

Article attribute

Article type

Publication date

Search Results

120 results

Results by year

Filters applied: . Clear all
Page 1
[Familial Vaquez' disease].
DINI E, VENTRUTO V, CIMINO R, DE ROSA L. DINI E, et al. Among authors: ventruto v. Minerva Med. 1961 Sep 19;52:3236-8. Minerva Med. 1961. PMID: 13886497 Italian. No abstract available.
A case of polimalformed fetus with a microdeletion of CTNNA3 gene.
Cancemi D, Urciuoli M, Morelli F, Lonardo MC, Lonardo V, Spampanato C, Ventruto M, Ventruto V, Sica C. Cancemi D, et al. Among authors: ventruto v. J Prenat Med. 2016 Jul-Dec;10(3-4):20-22. doi: 10.11138/jpm/2016.10.3.020. J Prenat Med. 2016. PMID: 28725342 Free PMC article.
A case of suspected teratogenic holoprosencephaly.
Stabile M, Bianco A, Iannuzzi S, Buonocore MC, Ventruto V. Stabile M, et al. Among authors: ventruto v. J Med Genet. 1985 Apr;22(2):147-9. doi: 10.1136/jmg.22.2.147. J Med Genet. 1985. PMID: 3989833 Free PMC article.
A malformed girl with a de novo proximal 6q deletion.
Lonardo F, Colantuoni M, Festa B, Gentile G, Guerritore G, Perone L, Santulli B, Ventruto V. Lonardo F, et al. Among authors: ventruto v. Ann Genet. 1988;31(1):57-9. Ann Genet. 1988. PMID: 3281572 Review.
[Karyotypes in paraproteinemias].
Ventruto V. Ventruto V. Haematologica. 1970;55(4):259-94. Haematologica. 1970. PMID: 4993379 Italian. No abstract available.
The gene for mesomelic dysplasia Kantaputra type is mapped to chromosome 2q24-q32.
Fujimoto M, Kantaputra PN, Ikegawa S, Fukushima Y, Sonta S, Matsuo M, Ishida T, Matsumoto T, Kondo S, Tomita H, Deng HX, D'urso M, Rinaldi MM, Ventruto V, Takagi T, Nakamura Y, Niikawa N. Fujimoto M, et al. Among authors: ventruto v. J Hum Genet. 1998;43(1):32-6. doi: 10.1007/s100380050033. J Hum Genet. 1998. PMID: 9609995
Ring (13),t(2;6) associated with familial fragile (16).
Ventruto V, Rinaldi A, Renda S, Stabile M, Rinaldi MM, Cavaliere ML, Conte N, Aveta V. Ventruto V, et al. J Med Genet. 1984 Jun;21(3):233. doi: 10.1136/jmg.21.3.233. J Med Genet. 1984. PMID: 6748026 Free PMC article. No abstract available.
120 results