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Henri Copin

Showing results (41-50 of 44) with videos related to

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American Journal of Medical Genetics. Part A|January 10, 2015
Clinical and molecular characterization of the 20q11.2 microdeletion syndrome: six new patientsGuillaume Jedraszak, Bénédicte Demeer, Michèle Mathieu-Dramard, et al.
European Journal of Medical Genetics|January 3, 2013
A novel microdeletion syndrome at 9q21.13 characterised by mental retardation, speech delay, epilepsy and characteristic facial featuresElise Boudry-Labis, Bénédicte Demeer, Cédric Le Caignec, et al.
European Journal of Medical Genetics|June 10, 2009
Cryptic genomic imbalances in de novo and inherited apparently balanced chromosomal rearrangements: array CGH study of 47 unrelated casesCaroline Schluth-Bolard, Bruno Delobel, Damien Sanlaville, et al.
American Journal of Medical Genetics. Part A|November 17, 2023
Cat eye syndrome: Clinical, cytogenetics and familial findings in a large cohort of 43 patients highlighting the importance of congenital heart disease and inherited casesGuillaume Jedraszak, Florence Jobic, Aline Receveur, et al.
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Showing results (41-50 of 44) with videos related to

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Pageof 5
You have reached the last page of results.This site can display upto 44 results.
American Journal of Medical Genetics. Part A|January 10, 2015
Clinical and molecular characterization of the 20q11.2 microdeletion syndrome: six new patientsGuillaume Jedraszak, Bénédicte Demeer, Michèle Mathieu-Dramard, et al.
European Journal of Medical Genetics|January 3, 2013
A novel microdeletion syndrome at 9q21.13 characterised by mental retardation, speech delay, epilepsy and characteristic facial featuresElise Boudry-Labis, Bénédicte Demeer, Cédric Le Caignec, et al.
European Journal of Medical Genetics|June 10, 2009
Cryptic genomic imbalances in de novo and inherited apparently balanced chromosomal rearrangements: array CGH study of 47 unrelated casesCaroline Schluth-Bolard, Bruno Delobel, Damien Sanlaville, et al.
American Journal of Medical Genetics. Part A|November 17, 2023
Cat eye syndrome: Clinical, cytogenetics and familial findings in a large cohort of 43 patients highlighting the importance of congenital heart disease and inherited casesGuillaume Jedraszak, Florence Jobic, Aline Receveur, et al.
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