31 results on '"Alfonsi, Melissa"'
Search Results
2. Mayer-Rokitansky-Küster-Hauser syndrome with 22q11.21 microduplication: a case report
3. Non-invasive prenatal screening: A 20-year experience in Italy
4. Case report of newborn with de novo partial trisomy 2q31.2–37.3 and monosomy 9p24.3
5. Prolonged in vitro expansion partially affects phenotypic features and osteogenic potential of ovine amniotic fluid-derived mesenchymal stromal cells
6. Isolation and Enrichment of Circulating Fetal Cells for NIPD: An Overview
7. Discovering a familial Xp11.4 microduplication: Does the mother matter?
8. Optimal cut-offs for down syndrome contingent screening in a population of 10 156 pregnant women
9. Optimal cut-offs for Down syndrome contingent screening in a population of 10,156 pregnant women: P2-70
10. Testing single/combined clinical categories on 5110 Italian patients with developmental phenotypes to improve array‐based detection rate
11. Yq Microdeletion in a Patient with VACTERL Association and Shawl Scrotum with Bifid Scrotum: A Real Pathogenetic Association or a Coincidence?
12. Discovering a familial Xp11.4 microduplication: Does the mother matter?
13. Sequential combined test, second trimester maternal serum markers, and circulating fetal cells to select women for invasive prenatal diagnosis
14. An 11.4-Mb Interstitial Deletion in a Fetus with No Apparent Phenotypic Alterations
15. Aneuploidy screening using circulating fetal cells in maternal blood by dual‐probe FISH protocol: a prospective feasibility study on a series of 172 pregnant women
16. 16p13.3 microduplication syndrome: A new characteristic case without intellectual disability
17. Case report of newborn with <bold><italic>de novo</italic></bold> partial trisomy 2q31.2-37.3 and monosomy 9p24.3.
18. Deletion 18p11.32p11.31 in a Child with Global Developmental Delay and Atypical, Drug-Resistant Absence Seizures
19. Human Second Trimester Amniotic Fluid Cells are Able to Create Embryoid Body-Like Structures in Vitro and to Show Typical Expression Profiles of Embryonic and Primordial Germ Cells
20. Array-CGH characterization of a prenatally detected de novo 46,X,der(Y)t(X;Y)(p22.3;q11.2) in a male fetus
21. De novo 9q33 microdeletion identified by array-comparative genomic hybridization in a foetus with sex reversal and congenital heart defects
22. Array-CGH characterization of a de novo t(X;Y)(p22;q11) in a female with short stature and mental retardation
23. Prenatal diagnosis of a family affected by brachydactyly type A1 with a mutation in IHH
24. 16q22.1 microdeletion detected by array-CGH in a family with mental retardation and lobular breast cancer
25. Indirect Co-Culture with Tendons or Tenocytes Can Program Amniotic Epithelial Cells towards Stepwise Tenogenic Differentiation
26. Mosaic 7q31 Deletion Involving FOXP2 Gene Associated With Language Impairment
27. P65: Complete imatinib-induced CML remission as evidenced by FISH predicts good outcome but it is not achieved in patients with der(9) deletion within 18-month follow up
28. An 11.4-Mb Interstitial Deletion in a Fetus with No Apparent Phenotypic Alterations.
29. Mayer-Rokitansky-Küster-Hauser syndrome with 22q11.21 microduplication: a case report.
30. Testing single/combined clinical categories on 5110 Italian patients with developmental phenotypes to improve array‐based detection rate.
31. De novo9q33 microdeletion identified by array-comparative genomic hybridization in a foetus with sex reversal and congenital heart defects
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