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 Custom Filters

Results by year

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

Year Number of Results
1976 1
1978 2
1979 1
1981 2
1982 3
1985 2
1986 1
1987 1
1988 4
1989 3
1990 3
1991 4
1992 1
1993 4
1994 3
1995 1
1996 2
1997 2
1998 3
1999 3
2000 2
2001 5
2002 1
2003 2
2004 1
2005 3
2006 1
2007 4
2008 6
2009 3
2010 1
2011 1
2013 1
2014 4
2015 4
2024 0

Publication date

Text availability

Article attribute

Article type

Additional filters

Article Language

Species

Sex

Age

Other

Search Results

79 results

Results by year

Filters applied: . Clear all
Page 1
[The prenatal diagnosis is not the eugenics].
Simon-Bouy B, Serre JL. Simon-Bouy B, et al. Among authors: serre jl. Gynecol Obstet Fertil. 2015 Apr;43(4):263-5. doi: 10.1016/j.gyobfe.2015.02.013. Epub 2015 Mar 26. Gynecol Obstet Fertil. 2015. PMID: 25819389 French. No abstract available.
Hypophosphatasia: molecular testing of 19 prenatal cases and discussion about genetic counseling.
Simon-Bouy B, Taillandier A, Fauvert D, Brun-Heath I, Serre JL, Armengod CG, Bialer MG, Mathieu M, Cousin J, Chitayat D, Liebelt J, Feldman B, Gérard-Blanluet M, Körtge-Jung S, King C, Laivuori H, Le Merrer M, Mehta S, Jern C, Sharif S, Prieur F, Gillessen-Kaesbach G, Zankl A, Mornet E. Simon-Bouy B, et al. Among authors: serre jl. Prenat Diagn. 2008 Nov;28(11):993-8. doi: 10.1002/pd.2088. Prenat Diagn. 2008. PMID: 18925618
FRAXAC2 instability.
Mornet E, Chateau C, Taillandier A, Montagnon M, Simon-Bouy B, Serre JL, Boué A. Mornet E, et al. Among authors: serre jl. Nat Genet. 1994 Jun;7(2):122-3. doi: 10.1038/ng0694-122b. Nat Genet. 1994. PMID: 7920626 No abstract available.
Existence of a genetic risk factor on chromosome 5q in Italian coeliac disease families.
Greco L, Babron MC, Corazza GR, Percopo S, Sica R, Clot F, Fulchignoni-Lataud MC, Zavattari P, Momigliano-Richiardi P, Casari G, Gasparini P, Tosi R, Mantovani V, De Virgiliis S, Iacono G, D'Alfonso A, Selinger-Leneman H, Lemainque A, Serre JL, Clerget-Darpoux F. Greco L, et al. Among authors: serre jl. Ann Hum Genet. 2001 Jan;65(Pt 1):35-41. doi: 10.1046/j.1469-1809.2001.6510035.x. Ann Hum Genet. 2001. PMID: 11415521
DNA polymorphism analysis in families with recurrence of free trisomy 21.
Pangalos CG, Talbot CC Jr, Lewis JG, Adelsberger PA, Petersen MB, Serre JL, Rethoré MO, de Blois MC, Parent P, Schinzel AA, et al. Pangalos CG, et al. Among authors: serre jl. Am J Hum Genet. 1992 Nov;51(5):1015-27. Am J Hum Genet. 1992. PMID: 1415248 Free PMC article.
Correlations of genotype and phenotype in hypophosphatasia.
Zurutuza L, Muller F, Gibrat JF, Taillandier A, Simon-Bouy B, Serre JL, Mornet E. Zurutuza L, et al. Among authors: serre jl. Hum Mol Genet. 1999 Jun;8(6):1039-46. doi: 10.1093/hmg/8.6.1039. Hum Mol Genet. 1999. PMID: 10332035
A molecular approach to dominance in hypophosphatasia.
Lia-Baldini AS, Muller F, Taillandier A, Gibrat JF, Mouchard M, Robin B, Simon-Bouy B, Serre JL, Aylsworth AS, Bieth E, Delanote S, Freisinger P, Hu JC, Krohn HP, Nunes ME, Mornet E. Lia-Baldini AS, et al. Among authors: serre jl. Hum Genet. 2001 Jul;109(1):99-108. doi: 10.1007/s004390100546. Hum Genet. 2001. PMID: 11479741
79 results