ISSN: 1552-4868

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American Journal of Medical Genetics - Seminars in Medical Genetics Q2 Unclaimed

Wiley-Liss Inc. United States

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American Journal of Medical Genetics - Seminars in Medical Genetics is a journal indexed in SJR in Genetics and Genetics (clinical) with an H index of 111. It has a price of 3000 €. It has an SJR impact factor of 0,814 and it has a best quartile of Q2. It is published in English. It has an SJR impact factor of 0,814.

Type: Journal

Type of Copyright:

Languages: English

Open Access Policy: Open Choice

Type of publications:

Publication frecuency: -

Categories: Genetics (Q2) Genetics (clinical) (Q2) Genetics (clinical) (Q2)

Price

3000 €

Inmediate OA

NPD

Embargoed OA

0 €

Non OA

Metrics

American Journal of Medical Genetics - Seminars in Medical Genetics

0,814

SJR Impact factor

111

H Index

55

Total Docs (Last Year)

248

Total Docs (3 years)

3233

Total Refs

761

Total Cites (3 years)

221

Citable Docs (3 years)

2.84

Cites/Doc (2 years)

58.78

Ref/Doc

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Genetic Epidemiology Q2
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Aims and Scope

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Renal manifestation of tuberous sclerosis complex

Serendipity or prepared mind? Recollections of the KOP translocation (1967) and of one form of Perrault syndrome

Suicidal behavior: Relationship between phenotype and serotonergic genotype

Etiologic yield of autistic spectrum disorders: A prospective study

Parental hopes, interventions, and survival of neonates with trisomy 13 and trisomy 18

Peering into the chasm: Improving the quality of clinical genetic services

A genetic approach to fracture epidemiology in childhood

Suicidal disorders: A nosological entity per se?

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The yield of subtelomeric FISH analysis in the evaluation of autistic spectrum disorders

History and geography of suicide: Could genetic risk factors account for the variation in suicide rates?

Cryptic telomere imbalance: A 15-year update

Improving genetic health care: A Northern New England pilot project addressing the genetic evaluation of the child with developmental delays or intellectual disability

Evidence-based medicine and practice guidelines: Application to genetics

Early pathogenesis of holoprosencephaly

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