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1. Monogenic conditions and central nervous system anomalies: A prospective study, systematic review and meta-analysis.

2. Cytogenetic analysis and visualization of genetic relationships in wild lilies.

3. Exploring the link between chromosomal polymorphisms and reproductive abnormalities.

4. 染色体微阵列技术在孕期羊水过多遗传病因诊断中的应用.

5. 一例胎儿淋巴水肿的家系基因遗传学分析.

6. Generation of a rhesus macaque induced pluripotent stem cell line (riPSC05) under feeder-free conditions.

7. Swyer Syndrome: Clinical Case of Gonadal Dysgenesis in a 15-year-old Girl

8. Exploring the link between chromosomal polymorphisms and reproductive abnormalities

9. Primary amenorrhoea - cytogenetic study in 40 Indian women.

10. Optimal prenatal genetic diagnostic approach for posterior fossa malformation: karyotyping, copy number variant testing, or whole-exome sequencing?

11. Chronic Myeloid Leukemia with a Rare Philadelphia Chromosome Variant Involving Chromosome 16.

12. 骨髓增生异常综合征相关的血脂异常分析.

13. Optimal prenatal genetic diagnostic approach for posterior fossa malformation: karyotyping, copy number variant testing, or whole-exome sequencing?

14. Role of Stem Cells in Sertoli Cell Only Syndrome.

15. 表型正常母亲二次孕育21-三体综合征患儿的遗传学分析.

16. Real-World Clinical Utility of Targeted RNA Sequencing in Leukemia Diagnosis and Management.

17. 6q14.1q16.3 缺失致胎儿多发畸形一例.

18. Single nucleotide polymorphism array (SNP-array) analysis for fetuses with abnormal nasal bone.

19. 45,X[2]/46,X,der(Y).ish Psu idic(Y)(q11.2)[38] mosaic karyotype in mixed gonadal dysgenesis: a case report and literature review

22. Transient Abnormal Myelopoiesis in a Down Syndrome Baby: A Case Report

24. Prenatal diagnosis of a trisomy 7 mosaic case: CMA, CNV-seq, karyotyping, interphase FISH, and MS-MLPA, which technique to choose?

25. Etiologic evaluation and pregnancy outcomes of fetal growth restriction (FGR) associated with structural malformations

26. Seeing Clowns with a Ring 20 Chromosome

27. Primary amenorrhoea - cytogenetic study in 40 Indian women

28. A novel two-staged deep learning based workflow for analyzable metaphase detection.

29. Prenatal diagnosis of a trisomy 7 mosaic case: CMA, CNV-seq, karyotyping, interphase FISH, and MS-MLPA, which technique to choose?

30. FISH联合染色体核型分析明确复发性流产家系遗传病因-例.

31. 相邻分离-2方式生成精子致胎儿染色体异常-例的遗传学分析.

32. 低深度全基因组测序技术在复发性流产遗传学 病因诊断中的应用.

33. Etiologic evaluation and pregnancy outcomes of fetal growth restriction (FGR) associated with structural malformations.

34. Smart Karyotyping Image Selection Based on Commonsense Knowledge Reasoning.

35. Cytogenetic evaluation of 661 prenatal samples.

36. Role of Interphase FISH Assay on Air-Dried Smears in Identifying Specific Structural Chromosomal Abnormalities among Pediatric Patients with Acute Leukemias.

37. Karyotyping of human chromosomes in metaphase images using faster R‐CNN and inception models.

38. 染色体微阵列分析在胎儿颅面畸形遗传病因诊断中的应用.

39. A cell line derived from heart of rainbow trout is refractory to Tilapia lake virus.

40. Hyperdiploid chromosomes in patients with B cell Acute lymphoblastic leukemia

41. Transient Abnormal Myelopoiesis in a Down Syndrome Baby: A Case Report.

42. Characteristics and clinical evaluation of X chromosome translocations

43. Cytogenetic profile and risk of transformation to acute myeloid leukemia (AML) in Indonesian patients with myelodysplastic syndrome (MDS): a pilot study [version 1; peer review: awaiting peer review]

44. Role of Genetics in Human Infertility.

45. Seeing Clowns with a Ring 20 Chromosome.

46. Mixed Gonadal Dysgenesis with 45,X/46,X,idic(Y)/46,XY Karyotype: A Case Report.

47. Characteristics and clinical evaluation of X chromosome translocations.

48. Congenital anomalies in fetal autopsy: An institutional experience.

49. The Urgency of Karyotyping Examination in Male Infertility Patients with Primary Hypogonadism.

50. The Discordance between G-Banding Karyotyping and Microarray in Structural Abnormality.

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