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

Filters

My NCBI Filters

Results by year

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

Year Number of Results
1973 1
1975 1
1978 3
1979 1
1982 1
1983 2
1984 4
1985 1
1986 1
1987 2
1988 2
1989 2
1991 3
1992 1
1993 5
1994 4
1996 1
1997 7
1998 4
1999 3
2000 5
2001 2
2002 5
2003 2
2004 6
2005 3
2006 3
2007 4
2008 8
2009 6
2010 3
2011 7
2012 5
2013 5
2014 9
2015 7
2016 8
2017 5
2018 6
2019 4
2020 7
2021 4
2022 3
2023 4
2024 3

Text availability

Article attribute

Article type

Publication date

PubMed for id: 871393

154 results

Results by year

Filters applied: . Clear all
Page 1
The utility of gene sequencing in identifying an underlying genetic disorder in prenatally suspected lower urinary tract obstruction.
Brar BK, Blakemore K, Hertenstein C, Miller JL, Miller KA, Shamseldin H, Maddirevula S, Hays T, Lianoglou B, Dukhovny S, Baker LA, Sparks TN, Wapner R, Alkuraya FS, Norton ME, Jelin AC; Fetal Sequencing Consortium. Brar BK, et al. Prenat Diagn. 2024 Feb;44(2):196-204. doi: 10.1002/pd.6425. Epub 2023 Aug 18. Prenat Diagn. 2024. PMID: 37594370
Atypical phenotype of a patient with Bardet-Biedl syndrome type 4.
Sloboda N, Lambert L, Ciorna V, Bruel AL, Tran Mau-Them F, Gomola V, Lemelle JL, Klein O, Camoin-Schweitzer MC, Magnavacca M, Legagneur C, Ezsto ML, Bonnet C, Philippe C, Leheup B. Sloboda N, et al. Mol Genet Genomic Med. 2022 May;10(5):e1869. doi: 10.1002/mgg3.1869. Epub 2022 Mar 23. Mol Genet Genomic Med. 2022. PMID: 35318824 Free PMC article.
Biallelic pathogenic variants in roundabout guidance receptor 1 associate with syndromic congenital anomalies of the kidney and urinary tract.
Münch J, Engesser M, Schönauer R, Hamm JA, Hartig C, Hantmann E, Akay G, Pehlivan D, Mitani T, Coban Akdemir Z, Tüysüz B, Shirakawa T, Dateki S, Claus LR, van Eerde AM; Genomics England Research Consortium; Smol T, Devisme L, Franquet H, Attié-Bitach T, Wagner T, Bergmann C, Höhn AK, Shril S, Pollack A, Wenger T, Scott AA, Paolucci S, Buchan J, Gabriel GC, Posey JE, Lupski JR, Petit F, McCarthy AA, Pazour GJ, Lo CW, Popp B, Halbritter J. Münch J, et al. Kidney Int. 2022 May;101(5):1039-1053. doi: 10.1016/j.kint.2022.01.028. Epub 2022 Feb 26. Kidney Int. 2022. PMID: 35227688 Free PMC article.
Chromosome abnormalities in dogs with disorders of sex development (DSD).
Szczerbal I, Nizanski W, Dzimira S, Nowacka-Woszuk J, Stachecka J, Biezynski J, Ligocka Z, Jagodka D, Fabian-Kurzok H, Switonski M. Szczerbal I, et al. Anim Reprod Sci. 2021 Jul;230:106771. doi: 10.1016/j.anireprosci.2021.106771. Epub 2021 May 19. Anim Reprod Sci. 2021. PMID: 34034132 Free article.
154 results