Clinical and molecular consequences of disease-associated de novo mutations in SATB2

Bengani, H (author)

Handley, M (author)

Alvi, M (author)

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Ibitoye, R (author)

Lees, M (author)

Lynch, SA (author)

Lam, W (author)

Fannemel, M (author)

Nordgren, A (author)

Karolinska Institutet

Malmgren, H (author)

Karolinska Institutet

Kvarnung, M (author)

Karolinska Institutet

Mehta, S (author)

McKee, S (author)

Whiteford, M (author)

Stewart, F (author)

Connell, F (author)

Clayton-Smith, J (author)

Mansour, S (author)

Mohammed, S (author)

Fryer, A (author)

Morton, J (author)

Grozeva, D (author)

Asam, T (author)

Moore, D (author)

Sifrim, A (author)

McRae, J (author)

Hurles, ME (author)

Firth, HV (author)

Raymond, FL (author)

Kini, U (author)

Nellaker, C (author)

FitzPatrick, DR (author)

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 (creator_code:org_t)

Elsevier BV, 2017

2017

English.

In: Genetics in medicine : official journal of the American College of Medical Genetics. - : Elsevier BV. - 1530-0366. ; 19:8, s. 900-908

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• Journal article (peer-reviewed)