35 results on '"Chen, Wen-lin"'
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2. Effect of Long‐Term Supplementation Lactobacillus paracasei on Body Composition in senescence‐accelerated mouse P8 (SAMP8)
3. Age‐Related Decrease of Neurotransmitters in Senescence‐Accelerated‐8 Mice
4. ChemInform Abstract: Synthesis of Multisubstituted Imidazoles via Copper-Catalyzed [3 + 2] Cycloadditions.
5. ChemInform Abstract: A Facile Protocol for N-Alkylation of Azoles Using KOtBu as Base under NBS-Promoted Conditions.
6. Prenatal diagnosis of the hypoplastic right heart syndrome with sex chromosome pentasomy (49,XXXXY)
7. Prenatal diagnosis of mosaic ring chromosome 4
8. Molecular cytogenetic analysis ofde novo dup(5)(q33.1q31.1) associated with abnormal perinatal findings
9. Prenatal diagnosis of pure distal 18q deletion
10. Prenatal diagnosis ofde novo t(2;18;14)(q33.1;q12.2;q31.2), dup(5)(q34q34), del(7)(p21.1p21.1), and del(10)(q25.3q25.3) and a review of the prenatally ascertainedde novo apparently balanced complex and multiple chromosomal rearrangements
11. Prenatal diagnosis of partial trisomy 10q (10q25.3→qter) and partial monosomy 18q (18q23→qter)
12. Perinatal findings of partial trisomy 13q (13q14.1→qter) resulting from paternal pericentric inversion of chromosome 13
13. Prenatal diagnosis of low-level mosaic trisomy 7 by amniocentesis
14. Prenatal diagnosis of partial trisomy 16q and distal 22q13 deletion associated with dolichocephaly and frontal bossing on second-trimester ultrasound
15. Prenatal diagnosis ofde novo proximal interstitial deletion of 9q and review of the literature of uncommon aneuploidies associated with increased nuchal translucency
16. Clinical, cytogenetic, and molecular analyses of prenatally diagnosed mosaic tetrasomy for distal chromosome 15q and review of the literature
17. Prenatal diagnosis of interstitially satellited 6p
18. Prenatal diagnosis of the distal 11q deletion and review of the literature
19. Prenatal diagnosis of premature centromere division–related mosaic variegated aneuploidy
20. Prenatal diagnosis ofde novo pure partial monosomy 4p (4p15.1 ? pter) in a growth-restricted fetus with a Greek warrior helmet face and unilateral facial cleft on three-dimensional ultrasound
21. Prenatal diagnosis ofde novo terminal deletion of chromosome 7q
22. Prenatal diagnosis of partial monosomy 18p(18p11.2?pter) and trisomy 21q(21q22.3?qter) with alobar holoprosencephaly and premaxillary agenesis
23. Prenatal diagnosis of mosaic ring chromosome 13 with anencephaly
24. Prenatal diagnosis and genetic analysis of X chromosome polysomy 49,XXXXY
25. Prenatal diagnosis and genetic analysis of double trisomy 48,XXX,+18
26. Prenatal diagnosis of partial trisomy 3p(3p23→pter) and monosomy 7q(7q36→qter) in a fetus with microcephaly alobar holoprosencephaly and cyclopia
27. Bilateral renal agenesis and fetal ascites in association with partial trisomy 13 and partial trisomy 16 due to a 3:1 segregation of maternal reciprocal translocation t(13;16)(q12.3; p13.2)
28. Prenatal diagnosis of partial trisomy 12 and partial trisomy 21 due to a 3:1 segregation of maternal reciprocal translocation t(12;21) (p13.3;q21)
29. Prenatal diagnosis of de novo t(2;18;14)(q33.1;q12.2;q31.2), dup(5)(q34q34), del(7)(p21.1p21.1), and del(10)(q25.3q25.3) and a review of the prenatally ascertained de novo apparently balanced complex and multiple chromosomal rearrangements.
30. Molecular cytogenetic analysis of de novo dup(5)(q33.1q31.1) associated with abnormal perinatal findings.
31. Prenatal diagnosis of partial trisomy 10q (10q25.3-->qter) and partial monosomy 18q (18q23-->qter).
32. Perinatal findings of partial trisomy 13q (13q14.1-->qter) resulting from paternal pericentric inversion of chromosome 13.
33. Prenatal diagnosis of de novo proximal interstitial deletion of 9q and review of the literature of uncommon aneuploidies associated with increased nuchal translucency.
34. Prenatal diagnosis of de novo pure partial monosomy 4p (4p15.1-->pter) in a growth-restricted fetus with a Greek warrior helmet face and unilateral facial cleft on three-dimensional ultrasound.
35. Prenatal diagnosis of de novo terminal deletion of chromosome 7q.
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