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

Year Number of Results
1968 1
1969 1
1970 1
1976 1
1993 2
1994 3
1996 4
1997 3
1998 2
1999 3
2000 5
2002 3
2003 1
2005 1
2006 1
2010 2
2011 1
2012 2
2014 1
2015 1
2017 1
2019 1
2020 1
2022 0
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40 results
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Page 1
[Next-generation DNA sequencing in clinical diagnostics].
Lacoste C, Fabre A, Pécheux C, Lévy N, Krahn M, Malzac P, Bonello-Palot N, Badens C, Bourgeois P. Lacoste C, et al. Among authors: malzac p. Arch Pediatr. 2017 Apr;24(4):373-383. doi: 10.1016/j.arcped.2017.01.008. Epub 2017 Feb 24. Arch Pediatr. 2017. PMID: 28242148 Review. French.
[What support for vulnerable people during confinement?].
Malzac P, Mathieu M, Einaudi MA. Malzac P, et al. Ethique Sante. 2020 Dec;17(4):220-225. doi: 10.1016/j.etiqe.2020.08.002. Epub 2020 Aug 16. Ethique Sante. 2020. PMID: 32837547 Free PMC article. French.
[Smith-Magenis syndrome].
Lacombe D, Moncla A, Malzac P, Mattei MG, Battin J. Lacombe D, et al. Among authors: malzac p. Arch Pediatr. 1997 May;4(5):438-42. doi: 10.1016/s0929-693x(97)86671-7. Arch Pediatr. 1997. PMID: 9230994 French.
[Genetic testing in the context of the revision of the French law on bioethics].
Bonneau D, Marlin S, Sanlaville D, Dupont JM, Sobol H, Gonzales M, Le Merrer M, Malzac P, Razavi F, Manouvrier S, Odent S, Stoppa-Lyonnet D. Bonneau D, et al. Among authors: malzac p. Pathol Biol (Paris). 2010 Oct;58(5):396-401. doi: 10.1016/j.patbio.2009.12.002. Epub 2010 Feb 8. Pathol Biol (Paris). 2010. PMID: 20116936 Review. French.
[Angelman syndrome].
Moncla A, Livet MO, Malzac P, Voelckel MA, Mattei MG, Mattei JF, Giraud F. Moncla A, et al. Among authors: malzac p. Arch Pediatr. 1994 Dec;1(12):1118-26. Arch Pediatr. 1994. PMID: 7849899 Review. French.
Risk estimation of uniparental disomy of chromosome 14 or 15 in a fetus with a parent carrying a non-homologous Robertsonian translocation. Should we still perform prenatal diagnosis?
Moradkhani K, Cuisset L, Boisseau P, Pichon O, Lebrun M, Hamdi-Rozé H, Maurin ML, Gruchy N, Manca-Pellissier MC, Malzac P, Bilan F, Audrezet MP, Saugier-Veber P, Fauret-Amsellem AL, Missirian C, Kuentz P, Egea G, Guichet A, Creveaux I, Janel C, Harzallah I, Touraine R, Goumy C, Joyé N, Puechberty J, Haquet E, Chantot-Bastaraud S, Schmitt S, Gosset P, Duban-Bedu B, Delobel B, Vago P, Vialard F, Gomes DM, Siffroi JP, Bonnefont JP, Dupont JM, Jonveaux P, Doco-Fenzy M, Sanlaville D, Le Caignec C. Moradkhani K, et al. Among authors: malzac p. Prenat Diagn. 2019 Oct;39(11):986-992. doi: 10.1002/pd.5518. Epub 2019 Aug 19. Prenat Diagn. 2019. PMID: 31273809 Free article.
[Decision-making in termination of pregnancy: a French perspective].
Gorincour G, Tassy S, Payot A, Philip N, Malzac P, Harlé JR, Mattei JF, Le Coz P. Gorincour G, et al. Among authors: malzac p. Gynecol Obstet Fertil. 2011 Apr;39(4):198-204. doi: 10.1016/j.gyobfe.2011.02.002. Epub 2011 Mar 23. Gynecol Obstet Fertil. 2011. PMID: 21435934 French.
Cortical myoclonus in Angelman syndrome.
Guerrini R, De Lorey TM, Bonanni P, Moncla A, Dravet C, Suisse G, Livet MO, Bureau M, Malzac P, Genton P, Thomas P, Sartucci F, Simi P, Serratosa JM. Guerrini R, et al. Among authors: malzac p. Ann Neurol. 1996 Jul;40(1):39-48. doi: 10.1002/ana.410400109. Ann Neurol. 1996. PMID: 8687190
The DYRK1A gene is a cause of syndromic intellectual disability with severe microcephaly and epilepsy.
Courcet JB, Faivre L, Malzac P, Masurel-Paulet A, Lopez E, Callier P, Lambert L, Lemesle M, Thevenon J, Gigot N, Duplomb L, Ragon C, Marle N, Mosca-Boidron AL, Huet F, Philippe C, Moncla A, Thauvin-Robinet C. Courcet JB, et al. Among authors: malzac p. J Med Genet. 2012 Dec;49(12):731-6. doi: 10.1136/jmedgenet-2012-101251. Epub 2012 Oct 25. J Med Genet. 2012. PMID: 23099646
40 results