American Journal Of Medical Genetics. Part B: Neuropsychiatric Genetics,volume 168,issue 7  (10-2015)

Period of time： 2015年7期

Publisher： John Wiley & Sons Inc

Founded in： 1977

Total resources： 28

E-ISSN： 1552-485x|168|7

ISSN： 1552-4841

Subject： Q3 Genetics

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American Journal Of Medical Genetics. Part B: Neuropsychiatric Genetics,volume 168,issue 7

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Gene set analysis: A step‐by‐step guide

American Journal Of Medical Genetics. Part B: Neuropsychiatric Genetics,volume 168,issue 7 , Vol. 168, Iss. 7, 2015-10 , pp. 517-527

John Wiley & Sons Inc

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Cumulative role of rare and common putative functional genetic variants at NPAS3 in schizophrenia susceptibility

American Journal Of Medical Genetics. Part B: Neuropsychiatric Genetics,volume 168,issue 7 , Vol. 168, Iss. 7, 2015-10 , pp. 528-535

John Wiley & Sons Inc

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The role of candidate‐gene CNTNAP2 in childhood apraxia of speech and specific language impairment

American Journal Of Medical Genetics. Part B: Neuropsychiatric Genetics,volume 168,issue 7 , Vol. 168, Iss. 7, 2015-10 , pp. 536-543

John Wiley & Sons Inc

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Significant association between rare IPO11‐HTR1A variants and attention deficit hyperactivity disorder in Caucasians

American Journal Of Medical Genetics. Part B: Neuropsychiatric Genetics,volume 168,issue 7 , Vol. 168, Iss. 7, 2015-10 , pp. 544-556

John Wiley & Sons Inc

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A genome‐wide association study of suicidal behavior

American Journal Of Medical Genetics. Part B: Neuropsychiatric Genetics,volume 168,issue 7 , Vol. 168, Iss. 7, 2015-10 , pp. 557-563

John Wiley & Sons Inc

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Quantifying naturalistic social gaze in fragile X syndrome using a novel eye tracking paradigm

American Journal Of Medical Genetics. Part B: Neuropsychiatric Genetics,volume 168,issue 7 , Vol. 168, Iss. 7, 2015-10 , pp. 564-572

John Wiley & Sons Inc

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Junctophilin 3 (JPH3) expansion mutations causing Huntington disease like 2 (HDL2) are common in South African patients with African ancestry and a Huntington disease phenotype

American Journal Of Medical Genetics. Part B: Neuropsychiatric Genetics,volume 168,issue 7 , Vol. 168, Iss. 7, 2015-10 , pp. 573-585

John Wiley & Sons Inc

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Brain calcification process and phenotypes according to age and sex: Lessons from SLC20A2, PDGFB, and PDGFRB mutation carriers

American Journal Of Medical Genetics. Part B: Neuropsychiatric Genetics,volume 168,issue 7 , Vol. 168, Iss. 7, 2015-10 , pp. 586-594

John Wiley & Sons Inc

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Fine mapping and whole‐exome sequencing of a familial cortical myoclonic tremor with epilepsy family

American Journal Of Medical Genetics. Part B: Neuropsychiatric Genetics,volume 168,issue 7 , Vol. 168, Iss. 7, 2015-10 , pp. 595-599

John Wiley & Sons Inc

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Comorbidity of intellectual disability confounds ascertainment of autism: implications for genetic diagnosis

American Journal Of Medical Genetics. Part B: Neuropsychiatric Genetics,volume 168,issue 7 , Vol. 168, Iss. 7, 2015-10 , pp. 600-608

John Wiley & Sons Inc

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