Kamran Moradkhani
Affiliations: | Université de Montpellier I. Faculté de médecine |
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Parents
Sign in to add mentor| Franck Pellestor | grad student | 2006 | Université de Montpellier I. Faculté de médecine | |
| (Étude cytogénétique de la ségrégation méiotique chez les hommes infertiles porteurs d'une translocation chromosomique) | ||||
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| Huynh MT, Riteau AS, Moradkhani K, et al. (2020) Structural abnormalities of chromosome 8 and Fetoplacental Discrepancy: A second case report and review of fetal phenotype of 8p inverted duplication deletion syndrome. European Journal of Medical Genetics. 104118 |
| Myers L, Blyth M, Moradkhani K, et al. (2019) Variable neurodevelopmental and morphological phenotypes of carriers with 12q12 duplications. Molecular Genetics & Genomic Medicine. e1013 |
| Moradkhani K, Cuisset L, Boisseau P, et al. (2019) Risk Estimation of Uniparental Disomy of Chromosome 14 or 15 in a Fetus with a Parent Carrying a Non-Homologous Robertsonian Translocation. Should We Still Perform Prenatal Diagnosis? Prenatal Diagnosis |
| Guterman S, Beneteau C, Redon S, et al. (2019) Prenatal findings in 1p36 deletion syndrome: new cases and a literature review. Prenatal Diagnosis |
| Conrad S, Demurger F, Moradkhani K, et al. (2019) 11q24.2q24.3 microdeletion in two families presenting features of Jacobsen syndrome, without intellectual disability: Role of FLI1, ETS1, and SENCR long noncoding RNA. American Journal of Medical Genetics. Part A |
| Lammers J, Reignier A, Splingart C, et al. (2018) Morphokinetic parameters in chromosomal translocation carriers undergoing preimplantation genetic testing. Reproductive Biomedicine Online |
| Bhatt SS, Manvelyan M, Moradkhani K, et al. (2014) Inverted segment size and the presence of recombination hot spot clusters matter in sperm segregation analysis. Cytogenetic and Genome Research. 142: 145-9 |
| Bhatt S, Moradkhani K, Mrasek K, et al. (2009) Breakpoint mapping and complete analysis of meiotic segregation patterns in three men heterozygous for paracentric inversions. European Journal of Human Genetics : Ejhg. 17: 44-50 |
| Bhatt S, Moradkhani K, Mrasek K, et al. (2007) Breakpoint characterization: a new approach for segregation analysis of paracentric inversion in human sperm. Molecular Human Reproduction. 13: 751-756 |
| Reboul MP, Tandonnet O, Biteau N, et al. (2006) Mosaic maternal uniparental isodisomy for chromosome 7q21-qter. Clinical Genetics. 70: 207-13 |