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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
2024 0

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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.
[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.
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
[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.
Expanding the HPSE2 Genotypic Spectrum in Urofacial Syndrome, A Disease Featuring a Peripheral Neuropathy of the Urinary Bladder.
Beaman GM, Lopes FM, Hofmann A, Roesch W, Promm M, Bijlsma EK, Patel C, Akinci A, Burgu B, Knijnenburg J, Ho G, Aufschlaeger C, Dathe S, Voelckel MA, Cohen M, Yue WW, Stuart HM, Mckenzie EA, Elvin M, Roberts NA, Woolf AS, Newman WG. Beaman GM, et al. Among authors: voelckel ma. Front Genet. 2022 Jun 23;13:896125. doi: 10.3389/fgene.2022.896125. eCollection 2022. Front Genet. 2022. PMID: 35812751 Free PMC article.
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.
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.
36 results