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51. Telomere status in chronic lymphocytic leukemia with TP53 disruption

52. ERCC1 and telomere status in breast tumours treated with neoadjuvant chemotherapy and their association with patient prognosis

53. A novel 2q14.1q14.3 deletion involvingGLI2andRNU4ATACgenes associated with partial corpus callosum agenesis and severe intrauterine growth retardation

54. Pregnancy outcomes in prenatally diagnosed 47, XXX and 47, XYY syndromes: a 30‐year French, retrospective, multicentre study

55. Mécanismes moléculaires de la surexpression de hTERT dans le cancer du sein

56. Microdélétion 17q12 et hernie diaphragmatique

63. Prenatal Screening of 21 Microdeletion/Microduplication Syndromes and Subtelomeric Imbalances by MLPA in Fetuses with Increased Nuchal Translucency and Normal Karyotype

64. Fetal skin fibroblasts: A cell model for studying the retinoid pathway in congenital diaphragmatic hernia

66. Abstract 550: Genomic instability and telomere characteristics as predictive biomarkers of therapeutic response in triple-negative breast cancer

67. De novo 2q36.1q36.3 interstitial deletion involving thePAX3andEPHA4genes in a fetus with spina bifida and cleft palate

68. TP53 Disruption and Telomere Instability In Chronic Lymphocytic Leukemia

69. An unusual clinical severity of 16p11.2 deletion syndrome caused by unmasked recessive mutation of CLN3

71. A novel 2q14.1q14.3 deletion involving GLI2 and RNU4ATAC genes associated with partial corpus callosum agenesis and severe intrauterine growth retardation.

82. De novo 2q36.1q36.3 interstitial deletion involving the PAX3 and EPHA4 genes in a fetus with spina bifida and cleft palate.

83. An unusual clinical severity of 16p11.2 deletion syndrome caused by unmasked recessive mutation of CLN3.

90. Cloning of the Genes Encoding Two Murine and Human Cochlear Unconventional Type I Myosins

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