Default: Prenatal Diagnosis

ISSN: 0197-3851

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Prenatal Diagnosis Q2 Unclaimed

John Wiley and Sons Ltd United Kingdom
Unfortunately this journal has not been claimed yet. For this reason, some information may be unavailable.

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: -


2395 €

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Prenatal Diagnosis


SJR Impact factor


H Index


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Total Docs (3 years)


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Total Cites (3 years)


Citable Docs (3 years)


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Aims and Scope

fetal, maternal, prenatal, counseling, blood, heart, detection, pregnancies, congenital, levels, genetic, determination, franceexperiences, fetuses, dysplasia, abnormalitieschromosomal, academic, determining, defectscreening, defects, defect, chromosome, chorionic, challenges, analysisabnormal, cellfree, cell, body, birth,

Best articles by citations

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

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

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

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

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

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Prenatal diagnosis of premature centromere division-related mosaic variegated aneuploidy

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

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

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

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Trisomy 13 manifested as hypoplastic left heart and other structural abnormalities

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

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

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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

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

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

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

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

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Charts of fetal size: kidney and renal pelvis measurements

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Sonographic findings in Beckwith-Wiedemann syndrome related toH19 hypermethylation

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

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

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

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

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

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