Default: Clinical Genetics

ISSN: 0009-9163

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Clinical Genetics Q1 Unclaimed

Wiley-Blackwell Publishing Ltd United Kingdom
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Clinical Genetics is a journal indexed in SJR in Genetics and Genetics (clinical) with an H index of 115. It has a price of 3650 €. It has an SJR impact factor of 1,236 and it has a best quartile of Q1. It is published in English. It has an SJR impact factor of 1,236.

Clinical Genetics focuses its scope in these topics and keywords: genetic, syndrome, overgrowth, mutation, ring, syndromic, patients, brca, x, molecular, ...

Type: Journal

Type of Copyright:

Languages: English

Open Access Policy: Open Choice

Type of publications:

Publication frecuency: -

Price

3650 €

Inmediate OA

NPD

Embargoed OA

0 €

Non OA

Metrics

Clinical Genetics

1,236

SJR Impact factor

115

H Index

188

Total Docs (Last Year)

548

Total Docs (3 years)

4900

Total Refs

1587

Total Cites (3 years)

445

Citable Docs (3 years)

2.67

Cites/Doc (2 years)

26.06

Ref/Doc

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Aims and Scope


genetic, syndrome, overgrowth, mutation, ring, syndromic, patients, brca, x, molecular, clustering, coloboma, dilemmafamilial, deletion, delineation, diagnosis, chromosomean, chromosomealumediated, children, alzheimer, ambras, aspects, bandlike, biobank, calcification, cases, causative, cdsn, channelopathyfunding, child,



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Estrogen receptor mutation in a girl with primary amenorrhea

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Bilateral complete radioulnar synostosis associated with ectrodactyly and sensorineural hearing loss: a variant of SHFM1

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The locus responsible for horizontal gaze palsy/progressive scoliosis and brainstem hypoplasia is refined to a 9-cM region on chromosome 11q23

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A systematic search for single nucleotide polymorphisms (SNPs) in the insulin receptor gene: association of an SNP with hyperlipidemia in Japanese type 2 diabetic subjects

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An interaction between the TaqIB polymorphism of cholesterol ester transfer protein and smoking is associated with changes in plasma high-density lipoprotein cholesterol levels in Turks

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A locus for autosomal recessive achromatopsia on human chromosome 8q

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MEFVmutations in Iranian Azeri Turkish patients with familial Mediterranean fever

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Genetic susceptibility to neural tube defect pregnancy varies with offspring phenotype

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Novel mutations in the CHST6 gene causing macular corneal dystrophy

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Association of a single nucleotide polymorphism in CPB2 encoding the thrombin-activable fibrinolysis inhibitor (TAFI) with blood pressure

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