Prader-Willi syndrome genetic subtypes and clinical neuropsychiatric diagnoses in residential care adults.

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Prader-Willi syndrome genetic subtypes and clinical neuropsychiatric diagnoses in residential care adults.

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2017 nî lūn-bûn

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2017年の論文

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2017年学术文章

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2017年学术文章

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2017年学术文章

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2017年学术文章

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2017年学术文章

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2017年学术文章

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2017年學術文章

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2017年學術文章

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Prader-Willi syndrome genetic ...... es in residential care adults.

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Prader-Willi syndrome genetic ...... es in residential care adults.

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Item

label

Prader-Willi syndrome genetic ...... es in residential care adults.

@en

Prader-Willi syndrome genetic ...... es in residential care adults.

@nl

prefLabel

Prader-Willi syndrome genetic ...... es in residential care adults.

@en

Prader-Willi syndrome genetic ...... es in residential care adults.

@nl

P1476

Prader-Willi syndrome genetic ...... ses in residential care adults

@en

P2093

N Weisensel

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S Ayala

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W Hossain

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P2860

Identification of four highly conserved genes between breakpoint hotspots BP1 and BP2 of the Prader-Willi/Angelman syndromes deletion region that have undergone evolutionary transposition mediated by flanking duplicons

The 15q11.2 BP1-BP2 microdeletion syndrome: a review

Molecular diagnosis of Prader-Willi and Angelman syndromes by methylation-specific melting analysis and methylation-specific multiplex ligation-dependent probe amplification

Behavioral differences among subjects with Prader-Willi syndrome and type I or type II deletion and maternal disomy

Prader-Willi syndrome: clinical genetics, cytogenetics and molecular biology

Large genomic duplicons map to sites of instability in the Prader-Willi/Angelman syndrome chromosome region (15q11-q13).

Molecular dissection of the Prader-Willi/Angelman syndrome region (15q11-13) by YAC cloning and FISH analysis.

Expression of 4 genes between chromosome 15 breakpoints 1 and 2 and behavioral outcomes in Prader-Willi syndrome

Prader-Willi syndrome: current understanding of cause and diagnosis.

Methylation-specific multiplex ligation-dependent probe amplification analysis of subjects with chromosome 15 abnormalities

P304

622-631

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scholarly article

P356

10.1111/CGE.13142

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P433

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P478

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Ann M Manzardo

Merlin Butler

P577

2018-02-05T00:00:00Z

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P698

28984907

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P932

5828945

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