340 results on '"Tachdjian, G."'
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2. La perte de la lysine demethylase KDM1A est la cause de l’hyperplasie macronodulaire bilatérale des surrénales GIP-dépendante
3. La perte de la lysine demethylase KDM1A est la cause de l’hyperplasie macronodulaire bilatérale des surrénales GIP-dépendante
4. Array comparative genomic hybridization analysis of small supernumerary marker chromosomes in human infertility
5. Oocyte in-vitro maturation: BCL2 mRNA content in cumulus cells reflects oocyte competency
6. Characterization of human PGD blastocysts with unbalanced chromosomal translocations and human embryonic stem cell line derivation
7. Évaluation de l’amniocentèse au troisième trimestre pour le dépistage des anomalies chromosomiques chez les patientes n’acceptant pas le risque de perte fœtale
8. Retrospective comparison of two media for in-vitro maturation of oocytes
9. Preimplantation genetic diagnosis for autosomal recessive polycystic kidney disease
10. Persistent Müllerian duct syndrome due to anti-Müllerian hormone receptor 2 microdeletions: a diagnostic challenge
11. Common 4q24 deletion in four cases of hematopoietic malignancy: early stem cell involvement?
12. Cellules souches embryonnaires et cellules pluripotentes induites, aspects biologiques et applications
13. Persistent Müllerian duct syndrome due to anti-Müllerian hormone receptor 2 microdeletions: a diagnostic challenge
14. Chromosomal breakpoints characterization of two supernumerary ring chromosomes 20
15. Interstitial deletion 6p22.3-p24.3 characterized by CGH array in a foetus with multiple malformations
16. Le diagnostic préimplantatoire couplé au typage HLA : l'expérience parisienne
17. Correlation between ultrasound and pathological examination in a prenatal diagnosis of Cri du Chat syndrome associated with partial trisomy 17q
18. Ultrastructural nuclear defects and increased chromosome aneuploidies in spermatozoa with elongated heads
19. Pure and complete trisomy 18p due to a supernumerary marker chromosome associated with moderate mental retardation
20. Analysis of laser effects on chromosomal structure by fluorescence in situ hybridization and image cytometry: Methodological approach for precise microdissection
21. Terminal 14q32.33 deletion: Genotype–phenotype correlation
22. Multiple displacement amplification improves PGD for fragile X syndrome
23. Molecular cytogenetic studies of Xq critical regions in premature ovarian failure patients
24. Prenatal diagnosis of a possible new middle interhemispheric variant of holoprosencephaly using sonographic and magnetic resonance imaging
25. A randomized double-blind controlled study on the efficacy of laser zona pellucida thinning on live birth rates in cases of advanced female age
26. Analysis of mtDNA variant segregation during early human embryonic development: a tool for successful NARP preimplantation diagnosis
27. Array comparative genomic hybridization profiling of first-trimester spontaneous abortions that fail to grow in vitro
28. Cytogenetic, molecular and testicular tissue studies in an infertile 45,X male carrying an unbalanced (Y;22) translocation: Case report
29. In vitro oocyte maturation for the treatment of infertility associated with polycystic ovarian syndrome: the French experience
30. Analysis of the 5′ flanking sequence of the Gγ globin gene by denaturing gradient gel electrophoresis confirms the heterogeneity of the Bantu βs haplotype
31. Deletion in the ABL gene resulting from a meiotic recombination of a maternal (3;22;9)(q22;q12;q34.1) translocation
32. Molecular cytogenetic analysis of a Xp21.3-pter deletion in a family with normal and short stature
33. Intérêt du génotypage du sexe fœtal dans le sang maternel dans les indications de diagnostic génétique préimplantatoire de sexe
34. PS1498 INCREASED RHOA ACTIVITY DUE TO A DISRUPTED FILAMIN A/ALPHAIIBBETA3 INTERACTION INDUCES MACROTHROMBOCYTOPENIA
35. Identification and characterization of a de novo partial trisomy 10p by comparative genomic hybridization (CGH)
36. Anomalies chromosomiques et architecture sous-clonale des adénomes somatotropes
37. Anomalías de la diferenciación sexual
38. SALL4 and NFATC2: Two major actors of interstitial 20q13.2 duplication
39. Transplantation of Macaca cynomolgus iPS-derived hematopoietic cells in NSG immunodeficient mice
40. Minisymposium with international participation «Epigenetic mechanisms of cancer development and prevention» was held on September 13–14, 2007 at the R.E. Kavetsky Institute of Experimental Pathology, Oncology and Radiobiology, National Academy of Sciences of Ukraine, Kyiv. More than 60 visitors, including young scientists and students, were the listeners of two-day program
41. Comparison of comparative genomic hybridization with conventional karyotype and classical fluorescence in situ hybridization for prenatal and postnatal diagnosis of unbalanced chromosome abnormalities
42. 295 HUMAN INDUCED PLURIPOTENT STEM CELLS (iPSCs) REPROGRAMMED WITH HOME-MADE-mRNAs: A TOOL FOR STEM-CELL DERIVED HEPATOCYTE STUDIES
43. P31 Successful preimplantation genetic diagnosis (PGD) test for Hirschsprung disease
44. Genome-wide association study and premature ovarian failure
45. Molecular cytogenetic characterization of a 4p15.1‐pter duplication and a 4q35.1‐qter deletion in a recombinant of chromosome 4 pericentric inversion
46. Aneuploidy testing by first polar body biopsy of human oocytes matured in vitro from polycystic ovary syndrome patients
47. Évaluation de l’amniocentèse au troisième trimestre pour le dépistage des anomalies chromosomiques chez les patientes n’acceptant pas le risque de perte fœtale
48. Risque d’absence de diagnostic prénatal d’une délétion 22q11.2 associée à une autre anomalie chromosomique dans une malformation cardiaque conotroncale
49. 7.014 PGD is a valuable reproductive option for couples at risk of transmitting autosomal dominant disorders with high clinical variability
50. Preimplantation diagnosis for mitochondrial DNA disorders: contribution to understanding mitochondrial DNA segregation during early human embryonic development
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