Keyword Connections

prenatal diagnosis

Journals

12

1 BMJ open

2 Bioinformatics

3 Health technology assessment (Winchester, England)

4 irish medical journal

5 Journal of clinical immunology

6 Optics express

7 surgery

8 american journal of obstetrics and gynecology

9 expert review of gastroenterology & hepatology

10 Hepatology

11 expert review of molecular diagnostics

12 Taiwanese journal of obstetrics & gynecology

Research Groups

0

No Research Group Connected

Bibliographies

61

1 Assessment of uteroplacental vascularisation in early first-trimester pregnancy with contrast-enhanced ultrasound and 3D power Doppler angiography: protocol for a prospective, cross-sectional, multicentre and non-randomised open study ("HOPE Study").

2 FunDMDeep-m6A: identification and prioritization of functional differential m6A methylation genes.

3 Dual-frequency CMOS terahertz detector with silicon-based plasmonic antenna.

4 MRI in the diagnosis of fetal developmental brain abnormalities: the MERIDIAN diagnostic accuracy study.

5 Impact of Introduction of a Clinical Pathway for the Management of Pyelonephritis on Obstetric Patients: a Quality Improvement Project

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

7 How does carrier status for recessive disorders influence reproductive decisions? A systematic review of the literature.

8 Zika Virus Detection in Amniotic Fluid and Zika-Associated Birth Defects.

9 A Patient-Held Smartcard With a Unique Identifier and an mHealth Platform to Improve the Availability of Prenatal Test Results in Rural Nigeria: Demonstration Study

10 ‘essential but not always available when needed’ – an interview study of physicians’ experiences and views regarding use of obstetric ultrasound in tanzania

11 conhecimento dos obstetras sobre a transmissão vertical da hepatite b knowledge of obstetricians about the vertical transmission of hepatitis b virus

12 legal ableism, interrupted: developing tort law & policy alternatives to wrongful birth & wrongful life claims

13 prenatal diagnosis of mos45,x/46,x,+mar in a fetus with normal male external genitalia and a literature review

14 prenatal diagnosis of congenitally corrected transposition of the great arteries

15 prenatal diagnosis of mosaic small supernumerary marker chromosome 17 associated with ventricular septal defect, developmental delay, and speech delay

16 molecular genetic characterization of a prenatally detected 1.484-mb xq13.3-q21.1 duplication encompassing atrx and a literature review of syndromic intellectual disability and congenital abnormalities in males with a duplication at xq13.3-q21.1

17 prenatal diagnosis and molecular cytogenetic characterization of a small supernumerary marker chromosome derived from chromosome 18 and associated with a reciprocal translocation involving chromosomes 17 and 18

18 detection of recurrent 4p16.3 microdeletion with 2p25.3 microduplication by multiplex ligation-dependent probe amplification and array comparative genomic hybridization in a fetus from a family with wolf–hirschhorn syndrome

19 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

20 prenatal hydrocolpos in a male

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

22 complete involution of prenatally-diagnosed fetal scalp hemangioma

23 prenatal diagnosis of hypomethylation at kvdmr1 and beckwith–wiedemann syndrome in a pregnancy conceived by intracytoplasmic sperm injection and in vitro fertilization and embryo transfer

24 prenatal diagnosis and molecular cytogenetic characterization of mosaicism for a small supernumerary marker chromosome derived from chromosome 21

25 mosaicismo inusual en un caso de diagnóstico prenatal citogenético

26 pcr in the first oropharynx aspirate of the newborn: a possible source for identification of congenital infection agents

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

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

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

30 Prenatal diagnosis of Duchenne and Becker muscular dystrophies: Underestimated problem of the secondary prevention of monogenetic disorders

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

32 Prenatal diagnosis of chromosomal aberrations by chromosomal microarray analysis in fetuses with ultrasound anomalies in the urinary system.

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

34 Prenatal diagnosis of birth defects and termination of pregnancy in Hunan Province, China.

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

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

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

38 prenatal diagnosis of iniencephaly: clues and pitfalls

39 prenatal diagnosis of low-level mosaicism for trisomy 2 associated with a favorable pregnancy outcome

40 prenatal diagnosis of cystic hygroma related to a deletion of 16q24.1 with haploinsufficiency of foxf1 and foxc2 genes

41 prenatal diagnosis of fetal peters’ plus syndrome: a case report

42 prenatal diagnosis of congenital paraesophageal hiatal hernia

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

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

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

46 prenatal diagnosis of cantrell’s pentalogy associated with agenesis of left limb in a twin pregnancy

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

48 prenatal diagnosis using fetal genetic material in maternal circulation

49 prenatal diagnosis of isolated hypospadias by using “tulip sign” with two and three-dimensional ultrasonography

50 prenatal diagnosis of wagr syndrome

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

52 prenatal diagnosis of fetal omphalocele by ultrasound: a comparison of two centuries

53 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

54 prenatal diagnosis and genetic analysis of a fetus with 47,xx, +21/46,xx mosaicism and xx/xy chimerism

55 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

56 prenatal diagnosis of a fetus with congenital heart defect and ring chromosome 14

57 prenatal diagnosis of low-level mosaicism for trisomy 21 with rare karyotype detected by noninvasive prenatal testing

58 prenatal diagnosis of zellweger syndrome: case report

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

60 prenatal diagnosis of concurrent achondroplasia and klinefelter syndrome

61 DNA prenatal diagnosis.