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Range of genetic mutations associated with severe non-syndromic sporadic intellectual disability: an exome sequencing study

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Range of genetic mutations associated with severe non-syndromic sporadic intellectual disability: an exome sequencing study is a paper indexed in PICO Portal from OpenAlex.

How many citations does Range of genetic mutations associated with severe non-syndromic sporadic intellectual disability: an exome sequencing study have?

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Range of genetic mutations associated with severe non-syndromic sporadic intellectual disability: an exome sequencing study has 1,076 citations in the OpenAlex counts PICO Portal stores.

When was Range of genetic mutations associated with severe non-syndromic sporadic intellectual disability: an exome sequencing study published?

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Range of genetic mutations associated with severe non-syndromic sporadic intellectual disability: an exome sequencing study has 2012 year in the PICO Portal index.

What is the open-access status of Range of genetic mutations associated with severe non-syndromic sporadic intellectual disability: an exome sequencing study?

PICO Portaloa status

Range of genetic mutations associated with severe non-syndromic sporadic intellectual disability: an exome sequencing study has green oa status in the PICO Portal index.

What is the DOI of Range of genetic mutations associated with severe non-syndromic sporadic intellectual disability: an exome sequencing study?

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The DOI for Range of genetic mutations associated with severe non-syndromic sporadic intellectual disability: an exome sequencing study is on the source record.

What is the PMID of Range of genetic mutations associated with severe non-syndromic sporadic intellectual disability: an exome sequencing study?

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The PMID for Range of genetic mutations associated with severe non-syndromic sporadic intellectual disability: an exome sequencing study is on the source record.

What is the OpenAlex record for Range of genetic mutations associated with severe non-syndromic sporadic intellectual disability: an exome sequencing study?

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The OpenAlex for Range of genetic mutations associated with severe non-syndromic sporadic intellectual disability: an exome sequencing study is on the source record.

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