Chromosomes in Ewing's sarcoma. II. Nonrandom additional changes, trisomy 8 and der(16)t(1;16)

Xq28 duplication including MECP2 in six unreported affected females: what can we learn for diagnosis and genetic counselling?

Clinical genetics·2016

NUP98 is rearranged in 3.8% of pediatric AML forming a clinical and molecular homogenous group with a poor prognosis.

Leukemia·2016

Homozygous Truncating Intragenic Duplication in TUSC3 Responsible for Rare Autosomal Recessive Nonsyndromic Intellectual Disability with No Clinical or Biochemical Metabolic Markers.

JIMD reports·2015

Pregnancy outcomes of prenatally diagnosed Turner syndrome: a French multicenter retrospective study including a series of 975 cases.

Prenatal diagnosis·2014

A French collaborative survey of 272 fetuses with 22q11.2 deletion: ultrasound findings, fetal autopsies and pregnancy outcomes.

Prenatal diagnosis·2014

Rare EGFR exon 18 and exon 20 mutations in non-small-cell lung cancer on 10 117 patients: a multicentre observational study by the French ERMETIC-IFCT network.

Annals of oncology : official journal of the European Society for Medical Oncology·2013

A pericentric inv(9)(p22q34) of the der(9)t(9;22)(q34;q11.2) is a recurrent secondary anomaly in Ph-positive leukemia.

Cancer genetics and cytogenetics·2010

Translocation (3;8)(q27;q24) in two cases of triple hit lymphoma.

Cancer genetics and cytogenetics·2010

Screening for DNA copy number aberrations in mucinous adenocarcinoma arising from the minor salivary gland: two case reports.

Cancer genetics and cytogenetics·2010

Screening for common copy-number variants in cancer genes.

Cancer genetics and cytogenetics·2010

Trisomy 17 in congenital plexiform (multinodular) cellular schwannoma.

Cancer genetics and cytogenetics·2010

Chromosomal alterations in Malaysian patients with nasopharyngeal carcinoma analyzed by comparative genomic hybridization.

Cancer genetics and cytogenetics·2010

FBXO6 ubiquitinates MAOA to promote monoamine neurotransmitter accumulation and tumor growth in HCC.

Journal of molecular cell biology·2026

Choreiform Movements and Pachymeningeal Enhancement in an Elderly Patient With Abnormal Blood Counts: A Case Report and Review of Literature.

Journal of investigative medicine high impact case reports·2026

Baseline circulating and tumor γδ T cells and early circulating CD8⁺PD1⁺ expansion predict response to Atezolizumab-bevacizumab in HCC.

Clinical cancer research : an official journal of the American Association for Cancer Research·2026

Endoscopic resection of benign airway tumors: A 21-year comparative study focusing on endobronchial hamartoma and leiomyoma.

Therapeutic advances in respiratory disease·2026

Complications after anterior closing-wedge high tibial osteotomy in anterior cruciate ligament reconstruction: A state-of-the-art technical review.

Knee surgery, sports traumatology, arthroscopy : official journal of the ESSKA·2026

Amino acid functionalization of Au-Ag@PDA with transferrin coupling for neuroprotection in mice with intracerebral hemorrhage.

Nanoscale·2026

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Chromosomes in Ewing's sarcoma. II. Nonrandom additional changes, trisomy 8 and der(16)t(1;16)

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Xq28 duplication including MECP2 in six unreported affected females: what can we learn for diagnosis and genetic counselling?

NUP98 is rearranged in 3.8% of pediatric AML forming a clinical and molecular homogenous group with a poor prognosis.

Homozygous Truncating Intragenic Duplication in TUSC3 Responsible for Rare Autosomal Recessive Nonsyndromic Intellectual Disability with No Clinical or Biochemical Metabolic Markers.

Pregnancy outcomes of prenatally diagnosed Turner syndrome: a French multicenter retrospective study including a series of 975 cases.

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Choreiform Movements and Pachymeningeal Enhancement in an Elderly Patient With Abnormal Blood Counts: A Case Report and Review of Literature.

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Endoscopic resection of benign airway tumors: A 21-year comparative study focusing on endobronchial hamartoma and leiomyoma.

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Chromosomes in Ewing's sarcoma. II. Nonrandom additional changes, trisomy 8 and der(16)t(1;16)

Abstract:

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