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C Turleau

Showing results (151-160 of 155) with videos related to

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Prenatal Diagnosis|June 22, 2000
Subtle familial unbalanced translocation t(8;11)(p23.2;p15.5) in two fetuses with Beckwith-Wiedemann featuresS Fert-Ferrer, A Guichet, J Tantau, et al.
European Journal of Medical Genetics|July 9, 2013
Monozygotic twins discordant for 18q21.2qter deletion detected by array CGH in amniotic fluidM Essaoui, M Nizon, M P Beaujard, et al.
Journal of Medical Genetics|April 16, 2002
Automated fluorescent genotyping detects 10% of cryptic subtelomeric rearrangements in idiopathic syndromic mental retardationM Rio, F Molinari, S Heuertz, et al.
European Journal of Human Genetics : EJHG|May 30, 2001
A novel automated strategy for screening cryptic telomeric rearrangements in children with idiopathic mental retardationL Colleaux, M Rio, S Heuertz, et al.
Annales De Genetique|January 1, 1997
Collaborative study of mosaic tetrasomy 12p or Pallister-Killian syndrome (nineteen fetuses or children)M Mathieu, C Piussan, F Thepot, et al.
Pageof 16

Showing results (151-160 of 155) with videos related to

Sort By:
Pageof 16
You have reached the last page of results.This site can display upto 155 results.
Prenatal Diagnosis|June 22, 2000
Subtle familial unbalanced translocation t(8;11)(p23.2;p15.5) in two fetuses with Beckwith-Wiedemann featuresS Fert-Ferrer, A Guichet, J Tantau, et al.
European Journal of Medical Genetics|July 9, 2013
Monozygotic twins discordant for 18q21.2qter deletion detected by array CGH in amniotic fluidM Essaoui, M Nizon, M P Beaujard, et al.
Journal of Medical Genetics|April 16, 2002
Automated fluorescent genotyping detects 10% of cryptic subtelomeric rearrangements in idiopathic syndromic mental retardationM Rio, F Molinari, S Heuertz, et al.
European Journal of Human Genetics : EJHG|May 30, 2001
A novel automated strategy for screening cryptic telomeric rearrangements in children with idiopathic mental retardationL Colleaux, M Rio, S Heuertz, et al.
Annales De Genetique|January 1, 1997
Collaborative study of mosaic tetrasomy 12p or Pallister-Killian syndrome (nineteen fetuses or children)M Mathieu, C Piussan, F Thepot, et al.
Pageof 16