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

Year Number of Results
1988 1
1989 2
1991 4
1992 3
1993 2
1994 2
1996 1
1997 1
1998 1
1999 2
2000 3
2003 1
2004 2
2005 1
2007 1
2010 2
2011 2
2012 2
2013 3
2015 1
2016 1
2019 1
2022 1
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36 results
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Page 1
Psychiatric genetic counseling: A mapping exercise.
Moldovan R, McGhee KA, Coviello D, Hamang A, Inglis A, Ingvoldstad Malmgren C, Johansson-Soller M, Laurino M, Meiser B, Murphy L, Paneque M, Papsuev O, Pawlak J, Rovira Moreno E, Serra-Juhe C, Shkedi-Rafid S, Laing N, Voelckel MA, Watson M, Austin JC. Moldovan R, et al. Among authors: voelckel ma. Am J Med Genet B Neuropsychiatr Genet. 2019 Dec;180(8):523-532. doi: 10.1002/ajmg.b.32735. Epub 2019 Jun 20. Am J Med Genet B Neuropsychiatr Genet. 2019. PMID: 31222934 Review.
[Angelman syndrome].
Moncla A, Livet MO, Malzac P, Voelckel MA, Mattei MG, Mattei JF, Giraud F. Moncla A, et al. Among authors: voelckel ma. Arch Pediatr. 1994 Dec;1(12):1118-26. Arch Pediatr. 1994. PMID: 7849899 Review. French.
French professionals in genetic counselor careers.
Cordier C, Taris N, De Pauw A, Sobol H, Philip N, Voelckel MA. Cordier C, et al. Among authors: voelckel ma. J Genet Couns. 2013 Dec;22(6):844-8. doi: 10.1007/s10897-013-9599-x. Epub 2013 May 21. J Genet Couns. 2013. PMID: 23689926
Genetic professionals' views on genetic counsellors: a French survey.
Cordier C, Taris N, Moldovan R, Sobol H, Voelckel MA. Cordier C, et al. Among authors: voelckel ma. J Community Genet. 2016 Jan;7(1):51-5. doi: 10.1007/s12687-015-0250-4. Epub 2015 Aug 18. J Community Genet. 2016. PMID: 26280995 Free PMC article.
Is the locus for Costello syndrome on 11p?
Kerr B, Mucchielli ML, Sigaudy S, Fabre M, Saunier P, Voelckel MA, Howard E, Elles R, Eden TO, Black GC, Philip N. Kerr B, et al. Among authors: voelckel ma. J Med Genet. 2003 Jun;40(6):469-71. doi: 10.1136/jmg.40.6.469. J Med Genet. 2003. PMID: 12807971 Free PMC article. No abstract available.
[Fragile X syndrome: current knowledge].
Pellissier MC, Voelckel MA, Mattei JF. Pellissier MC, et al. Among authors: voelckel ma. Pediatrie. 1992;47(11):743-50. Pediatrie. 1992. PMID: 1364151 Review. French.
Loss-of-function mutations in HPSE2 cause the autosomal recessive urofacial syndrome.
Pang J, Zhang S, Yang P, Hawkins-Lee B, Zhong J, Zhang Y, Ochoa B, Agundez JA, Voelckel MA, Fisher RB, Gu W, Xiong WC, Mei L, She JX, Wang CY. Pang J, et al. Among authors: voelckel ma. Am J Hum Genet. 2010 Jun 11;86(6):957-62. doi: 10.1016/j.ajhg.2010.04.016. Am J Hum Genet. 2010. PMID: 20560209 Free PMC article.
36 results