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
1952 3
1953 1
1954 4
1956 2
1957 10
1958 4
1959 4
1960 10
1961 11
1962 5
1964 1
1965 13
1966 57
1967 64
1968 81
1969 83
1970 102
1971 110
1972 106
1973 106
1974 144
1975 108
1976 108
1977 95
1978 101
1979 84
1980 80
1981 72
1982 81
1983 96
1984 99
1985 111
1986 116
1987 103
1988 118
1989 133
1990 168
1991 220
1992 263
1993 258
1994 258
1995 261
1996 285
1997 295
1998 313
1999 348
2000 301
2001 330
2002 380
2003 367
2004 368
2005 422
2006 434
2007 487
2008 472
2009 491
2010 489
2011 582
2012 666
2013 749
2014 726
2015 697
2016 679
2017 653
2018 594
2019 267
2020 2
Text availability
Article attribute
Article type
Publication date

Search Results

14,238 results
Results by year
Filters applied: . Clear all
Page 1
Non-invasive prenatal testing
Harraway J. Aust Fam Physician 2017. PMID 29036772 Free article.
Wolf-Hirschhorn syndrome: A review and update
Battaglia A, et al. Am J Med Genet C Semin Med Genet 2015 - Review. PMID 26239400
Our aim is to provide genotype-specific anticipatory guidance and recommendations to families of individuals with a diagnosis of WHS. ...
Our aim is to provide genotype-specific anticipatory guidance and recommendations to families of individuals with a diagnosis of WHS. …
Update in non-invasive prenatal testing
D'ambrosio V, et al. Minerva Ginecol 2019 - Review. PMID 30318870
Non-invasive prenatal testing (NIPT) has revolutionized the approach to prenatal diagnosis and, to date, it is the most superior screening method for the common autosomal aneuploidies, mostly trisomy 21. ...
Non-invasive prenatal testing (NIPT) has revolutionized the approach to prenatal diagnosis and, to date, it is the most superior scre …
Common genetic and epigenetic syndromes
Adams DJ and Clark DA. Pediatr Clin North Am 2015 - Review. PMID 25836705
Rapid and simple prenatal diagnosis of common chromosome disorders: advantages and disadvantages of the molecular methods FISH and QF-PCR.
Hultén MA, et al. Reproduction 2003 - Review. PMID 12968936
Molecular techniques have been developed for prenatal diagnosis of the most common chromosome disorders (trisomies 21, 13, 18 and sex chromosome aneuploidies) where results are available within a day or two. ...These women comprise the majority of those currently offered prenatal diagnosis with respect to fetal chromosome disorders and if introduced on a larger scale, the use of FISH and QF-PCR would lead to substantial economical savings. ...
Molecular techniques have been developed for prenatal diagnosis of the most common chromosome disorders (trisomies 21, …
Prospective chromosome analysis of 3429 amniocentesis samples in China using copy number variation sequencing.
Wang J, et al. Am J Obstet Gynecol 2018. PMID 29852155
BACKGROUND: Next-generation sequencing is emerging as a viable alternative to chromosome microarray analysis for the diagnosis of chromosome disease syndromes. ...Based on key performance criteria, copy number variation sequencing appears to be a well-suited methodology for first-tier diagnosis of pregnant women in the general population at risk of having a suspected fetal chromosome abnormality....
BACKGROUND: Next-generation sequencing is emerging as a viable alternative to chromosome microarray analysis for the diagnosis
Cri du chat syndrome: a critical review
Rodríguez-Caballero A, et al. Med Oral Patol Oral Cir Bucal 2010 - Review. PMID 20038906 Free article.
A new syndrome was identified in 1963, when Lejeune et al. reported a genetic disease resulting from a partial or total deletion on the short arm of chromosome 5 (5p-) and named it the cri du chat syndrome (CdCS). ...
A new syndrome was identified in 1963, when Lejeune et al. reported a genetic disease resulting from a partial or total deletion on the shor …
Congenital heart disease and cardiac procedural outcomes in patients with trisomy 21 and Turner syndrome
Morales-Demori R. Congenit Heart Dis 2017 - Review. PMID 28736822
According to the American Academy of Pediatrics, every patient with these genetic disorders should have a postnatal echocardiogram. ...However, the spectrum of CHD in these genetic disorders is wider than those mentioned lesions. More cardiac surgical procedures are offered to these patients and that has influenced positively their life expectancy for some CHD conditions. ...
According to the American Academy of Pediatrics, every patient with these genetic disorders should have a postnatal echocardiogram. . …
14,238 results
Jump to page
Feedback