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AC Tabet

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Francesca R Grati; Fabien Guimiot; Laurence Loeuillet; Federico Maggi; Francesca Malvestiti; Livia Marcato; Anna Maria Ruggeri; Giuseppe Simoni; Howard R Slater; AC Tabet; Azzedine Aboura; Eleonore Blondeel; Simona De Toffol; Celine Dupont; Devika Ganesamoorthy; Denise Molina Gomes; Robert Wainer; François Vialard
Application of a new molecular technique for the genetic evaluation of products of conception.
Jérôme Rambaud; AC Tabet; Alain Verloes; Isabelle Marey; Laurence Perrin-Sabourin; Azzedine Aboura; Brigitte Benzacken; Yline Capri; Céline Dupont; Marion Gérard
Nail and phalangeal agenesis in a patient with 4pter and 9pter duplication.
Céline Dupont; Azzedine Aboura; C Baumann; Brigitte Benzacken; P Bourdoncle; Fabien Guimiot; Dominique Le Tessier; C Lebugle; I Marey; L Perrin; D Smiljkovski; AC Tabet; Jean-Michel Dupont
3D position of pericentromeric heterochromatin within the nucleus of a patient with ICF syndrome.

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All Publications

2013: Francesca R Grati; Fabien Guimiot; Laurence Loeuillet; Federico Maggi; Francesca Malvestiti; Livia Marcato; Anna Maria Ruggeri; Giuseppe Simoni; Howard R Slater; AC Tabet; Azzedine Aboura; Eleonore Blondeel; Simona De Toffol; Celine Dupont; Devika Ganesamoorthy; Denise Molina Gomes; Robert Wainer; François Vialard
Application of a new molecular technique for the genetic evaluation of products of conception.
Prenatal diagnosis 2013;33(1):32-41.
2012: Jérôme Rambaud; AC Tabet; Alain Verloes; Isabelle Marey; Laurence Perrin-Sabourin; Azzedine Aboura; Brigitte Benzacken; Yline Capri; Céline Dupont; Marion Gérard
Nail and phalangeal agenesis in a patient with 4pter and 9pter duplication.
American journal of medical genetics. Part A 2012;158A(9):2277-82.
2012: Céline Dupont; Azzedine Aboura; C Baumann; Brigitte Benzacken; P Bourdoncle; Fabien Guimiot; Dominique Le Tessier; C Lebugle; I Marey; L Perrin; D Smiljkovski; AC Tabet; Jean-Michel Dupont
3D position of pericentromeric heterochromatin within the nucleus of a patient with ICF syndrome.
Clinical genetics 2012;82(2):187-92.
2012: Marie Devernay; Emmanuel Ecosse; Bénédicte Gérard; Lamia Kerdjana; AC Tabet; Azzedine Aboura; Brigitte Benzacken; Diana Bolca; Joël Coste; Jean-Claude Carel
Parental origin of the X-chromosome does not influence growth hormone treatment effect in Turner syndrome.
The Journal of clinical endocrinology and metabolism 2012;97(7):E1241-8.
2012: Andrée Delahaye; Séverine Drunat; Céline Dupont; Jacques Elion; Laurence Faivre; Frédérique Gatelais; Marion Gérard-Blanluet; Pierre Gressens; Sophie Kaltenbach; Marie Legendre; Sandrine Passemard; Eva Pipiras; Samuel Quentin; AC Tabet; Annick Toutain; Alain Verloes; Azzedine Aboura; Serge Amselem; Pierre Bitoun; Nicolas Chassaing; Brigitte Benzacken
Genomic imbalances detected by array-CGH in patients with syndromal ocular developmental anomalies.
European journal of human genetics : EJHG 2012;20(5):527-33.
2012: AC Tabet; Alain Verloes; Frédérique Amsellem; Brigitte Benzacken; Richard Delorme; Marion Leboyer; Marion Pilorge; Jean-Marc Pinard; Catalina Betancur
Autism multiplex family with 16p11.2p12.2 microduplication syndrome in monozygotic twins and distal 16p11.2 deletion in their brother.
European journal of human genetics : EJHG 2012;20(5):540-6.
2007: S Kanafani; Azzedine Aboura; Eva Pipiras; Lionel Carbillon; AC Tabet; C Largillière; C Garel; P Gressens; Martine Bucourt; Isabelle Cedrin-Durnerin; Eric Lachassinne; C Roumegoux; Michèle Uzan; Jean-Noel Hugues; Jean-Philippe Wolf; Brigitte Benzacken
Semilobar holoprosencephaly prenatal diagnosis: an unexpected complex rearrangement in a de novo apparently balanced reciprocal translocation on karyotype.
Prenatal diagnosis 2007;27(3):279-84.
2001: AC Tabet; Azzedine Aboura; M C Dauge; François Audibert; Aurore Coulomb; A Batallan; M H Couturier-Turpin; G Feldmann; Gérard Tachdjian
Cytogenetic analysis of trophoblasts by comparative genomic hybridization in embryo-fetal development anomalies.
Prenatal diagnosis 2001;21(8):613-8.
2001: AC Tabet; Jean-Michel Dupont; Aziza Lebbar; M H Couturier-Turpin; G Feldmann; Didier Rabineau
Heteromorphism 18ph+ : with or without reproductive consequences?
Annales de génétique 2001;44(3):139-42.