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Congenital Anomalies
United Kingdom · Wiley-Blackwell Publishing L...
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Congenital Anomalies

Congenital Anomalies is a journal indexed in SJR in Medicine (miscellaneous) and Developmental Biology with an H index of 32. It has a best quartile of -. It is published in English.

ISSN: 0914-3505
Publisher: Wiley-Blackwell Publishing Ltd
Category: Medicine (miscellaneous)
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schedule CountryOfPapers database fields
SJR Impact Factor trending_up
0 -
H-index 32
Acceptance rate pie_chart
35%
Source Acceptance_Rate
Time to publication hourglass_top
NPD
Field NPD
Publication cost (APC) payments
NPD Subscription
Non-OA path NPD

Metrics

Scimago and CountryOfPapers database fields

SJR Impact

0

H-index

32

Docs (year)

16

Docs 3y

39

Total refs

255

Cites 3y

50

Citable 3y

37

Cites/Doc 2y

0.92

Ref/Doc

15.94

Immediate OA

—

Embargoed OA

NPD

Non OA / Submission

—

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Best articles by citations

Morphological and immunohistochemical studies on cleft palates induced by 2,3,7,8-tetrachlorodibenzo-p-dioxin in mice

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Sex ratio of congenital abnormalities in the function of maternal age: A population-based study

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Vesicular swelling in the cervical region with lymph sac formation in human embryos

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Value of the small cohort study including a physical examination for minor structural defects in identifying new human teratogens

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Toward a new stage of Congenital Anomalies

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Studies on preliminary concentration methods for recovery of fetal nucleated red blood cells in maternal blood

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Sonic hedgehog expression in Gli3 depressed mouse embryo, Pdn/Pdn

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Urorectal septum malformation sequence: A report of seven cases

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No increases in the rate of undescended testis in Hungary during the last 50 years: A population-based study

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Necessity to establish new risk assessment and risk communication for human fetal exposure to multiple endocrine disruptors in Japan

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Myocardial infarction in a neonate with left-sided congenital diaphragmatic hernia

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Mouseexo uterodevelopment system: Protocol and troubleshooting

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Late-presenting congenital diaphragmatic hernia in a child with TMEM70 deficiency

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Large fontanelles are a shared feature of haploinsufficiency of RUNX2 and its co-activator CBFB

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