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WPRIM Management System>
DCMS
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Journal of Zhejiang University. Medical sciences
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2019
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48
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4
Volume:
48
Issue:
4
1. Single nucleotide polymorphism microarray in prenatal diagnosis of fetuses with absent nasal bone.
Page:414—419
2. Association of maternal age with fetal sex chromosome aneuploidies.
Page:409—413
3. Noninvasive prenatal screening for twin pregnancy: an analysis of 2057 cases.
Page:403—408
4. Genetic analysis of a fetus with multiple malformations caused by complex translocations of four chromosomes.
Page:397—402
5. Genetic analysis of newborns with abnormal metabolism of 3-hydroxyisovalerylcarnitine.
Page:390—396
6. Analysis of Alport syndrome induced by type IV collagen alpha 5 gene mutation in two families.
Page:384—389
7. Genetic analysis of a family of Van der Woude syndrome.
Page:378—383
8. Genetic study of a family of neuronal ceroid lipofuscinosis caused by a heterozygous mutation of gene.
Page:373—377
9. Genetic analysis and prenatal diagnosis of a sporadic family with neurofibromatosis type 1.
Page:367—372
10. Progress on evaluation, diagnosis and management of disorders of sex development.
Page:358—366
11. Advances in newborn screening and immune system reconstitution of severe combined immunodeficiency.
Page:351—357
12. Screening for hereditary tyrosinemia and genotype analysis in newborns.
Page:459—464
13. Assessment of fetal superior mesenteric artery and vein by three-dimensional power Doppler sonography.
Page:453—458
14. Ultrasound diagnosis of left inferior vena cava and double inferior vena cava in fetus.
Page:446—452
15. Prenatal diagnosis and management of fetal hepatic hemangioma.
Page:439—445
16. Prognosis of fetuses with cystichygroma and nuchal translucency/nuchal fold thickening on prenatal echography.
Page:434—438
17. Prenatal diagnosis and pregnancy outcomes of 22q11.2 duplication syndrome: analysis of 8 cases.
Page:429—433
18. Application of single nucleotide polymorphism microarray in clinical diagnosis of intellectual disability or retardation.
Page:420—428