ISSN: 0197-3851

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Prenatal Diagnosis Q2 Unclaimed

John Wiley and Sons Ltd United Kingdom

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Prenatal Diagnosis is a journal indexed in SJR in Obstetrics and Gynecology and Genetics (clinical) with an H index of 106. It has a price of 2395 €. It has an SJR impact factor of 0,79 and it has a best quartile of Q2. It is published in English. It has an SJR impact factor of 0,79.

Prenatal Diagnosis focuses its scope in these topics and keywords: fetal, maternal, prenatal, counseling, blood, heart, detection, pregnancies, congenital, levels, ...

Type: Journal

Type of Copyright:

Languages: English

Open Access Policy: Open Choice

Type of publications:

Publication frecuency: -

Categories: Obstetrics and Gynecology (Q2) Genetics (clinical) (Q3)

Price

2395 €

Inmediate OA

NPD

Embargoed OA

0 €

Non OA

Metrics

0,79

SJR Impact factor

106

H Index

196

Total Docs (Last Year)

585

Total Docs (3 years)

7048

Total Refs

1628

Total Cites (3 years)

528

Citable Docs (3 years)

2.9

Cites/Doc (2 years)

35.96

Ref/Doc

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Other journals with similar parameters

Journal of Assisted Reproduction and Genetics Q2
Journal of Pregnancy Q2
American Journal of Reproductive Immunology Q2
Journal of Reproductive Immunology Q2
BMC Women's Health Q2

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Aims and Scope

Best articles by citations

Prenatal diagnosis of human cytomegalovirus by culture and polymerase chain reaction: 98 pregnancies leading to congenital infection

Providing letters and audiotapes to supplement a prenatal diagnostic consultation: effects on later distress and recall

Prenatal diagnosis of mos46,X,del(Y)(q11.2)/45,X by cytogenetic and molecular studies with multiplex STR analysis

The influence of needle and syringe size on chorionic villus sampling of term placentae: a randomised trial

Prenatal diagnosis of mosaic trisomy 16 associated with congenital diaphragmatic hernia and elevated maternal serum alpha-fetoprotein and human chorionic gonadotrophin

Prenatal diagnosis of premature centromere division-related mosaic variegated aneuploidy

Ductus venosus assessment at the time of nuchal translucency measurement in the detection of fetal aneuploidy

Medically assisted reproduction and second-trimester maternal serum marker screening for Down syndrome

Prenatal diagnosis of sacrococcygeal teratoma with constitutional partial monosomy 7q/trisomy 2p

Trisomy 13 manifested as hypoplastic left heart and other structural abnormalities

Trisomy 13 mosaicism: study of serial cytogenetic changes in a case from early pregnancy to infancy

Prenatal diagnosis of the distal 11q deletion and review of the literature

SHOW MORE ARTICLES

The impact of correcting for smoking status when screening for chromosomal anomalies using maternal serum biochemistry and fetal nuchal translucency thickness in the first trimester of pregnancy

Multi-channel magnetocardiography for detecting beat morphology variations in fetal arrhythmias

Mosaic trisomy 13 on chorionic villi in a fetus with body wall complex: fortuitous association or pathogenic hypothesis?

Description of misdiagnosis and missed diagnosis of fetal complex heart malformations by prenatal echocardiography combined with postnatal cardiovascular casting

Pallister-Killian syndrome presenting through nuchal oedema: cytogenetic investigation and parental origin by molecular analysis in a new case

Charts of fetal size: kidney and renal pelvis measurements

Sonographic findings in Beckwith-Wiedemann syndrome related toH19 hypermethylation

Familial occurrence of isolated nonseptated nuchal cystic hygromata in midtrimester of pregnancy

Radiographic and genetic diagnosis of sporadic hypochondroplasia early in the neonatal period

Ultrasonography of the fetal brainstem: a biometric and anatomical, multioperator, cross-sectional study of 913 fetuses of 21-36 weeks of gestation

Culture of endothelial cells isolated from maternal blood using anti-CD105 and CD133

Uptake of prenatal screening for chromosomal anomalies: impact of test results in a previous pregnancy