Keyword Connections

prenatal diagnosis

Journals

0

No Journal Connected

Research Groups

0

No Research Group Connected

Bibliographies

21

1 Intrapartum antibiotic prophylaxis for the prevention of perinatal group B streptococcal disease: experience in the United States and implications for a potential group B streptococcal vaccine

2 A method for non-invasive prenatal diagnosis of monogenic autosomal recessive disorders.

3 Validation of Extensive Next-Generation Sequencing Method for Monogenic Disorder Analysis on Cell-Free Fetal DNA: Noninvasive Prenatal Diagnosis

4 A Cell-free DNA Barcode-Enabled Single-Molecule Test for Noninvasive Prenatal Diagnosis of Monogenic Disorders: Application to β-Thalassemia

5 Clinical and Molecular Features of Chronic Granulomatous Disease in Mainland China and a XL-CGD Female Infant Patient After Prenatal Diagnosis.

6 Assessment of 6 STR loci for prenatal diagnosis of Duchenne Muscular Dystrophy.

7 Rapid prenatal diagnosis of Facioscapulohumeral Muscular Dystrophy 1 by combined Bionano optical mapping and karyomapping.

8 Gynecology and Oncology Fetal Myofibromatosis: A Challenge for Prenatal Diagnosis Mini Review of the English Literature

9 partial trisomy 10q (10q25.1 →qter) and partial monosomy 13q (13q34→qter) presenting with fetal pyelectasis: prenatal diagnosis and array comparative genomic hybridization characterization

10 diagnóstico prenatal no invasivo: Ácidos nucleicos de origen fetal en sangre materna non invasive prenatal diagnosis: fetal nucleic acid analysis in maternal blood

11 the role of rnas and micrornas in non-invasive prenatal diagnosis

12 non-invasive prenatal diagnosis in the management of preimplantation genetic diagnosis pregnancies

13 first-trimester prenatal diagnosis of ellis–van creveld syndrome

14 first trimester ultrasound in prenatal diagnosis—part of the turning pyramid of prenatal care

15 mutation analysis of gjb2 gene and prenatal diagnosis in a non-syndromic deafness family

16 cmv by rt-pcr in prenatal diagnosis the detection of cmv in amniotic fluid and cervicovaginal smear samples by real-time pcr assay in prenatal diagnosis

17 mosaic ring chromosome 21, monosomy 21, and isodicentric ring chromosome 21: prenatal diagnosis, molecular cytogenetic characterization, and association with 2-mb deletion of 21q21.1–q21.2 and 5-mb deletion of 21q22.3

18 de novo unbalanced translocation resulting in monosomy for distal 5p (5p14.1 → pter) and 14q (14q32.31 → qter) associated with fetal nuchal edema, microcephaly, intrauterine growth restriction, and single umbilical artery: prenatal diagnosis and molecular cytogenetic characterization

19 mosaic trisomy 7 at amniocentesis: prenatal diagnosis and molecular genetic analyses

20 three-dimensional ultrasound in the prenatal diagnosis of osteogenesis imperfecta

21 DNA prenatal diagnosis.