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Defining the clinical phenotype of Saul-Wilson syndrome

Ferreira, CR (author)
Zein, WM (author)
Huryn, LA (author)
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Merker, A (author)
Karolinska Institutet
Berger, SI (author)
Wilson, WG (author)
Tiller, GE (author)
Wolfe, LA (author)
Merideth, M (author)
Carvalho, DR (author)
Duker, AL (author)
Bratke, H (author)
Haug, MG (author)
Rohena, L (author)
Hove, HB (author)
Xia, ZJ (author)
Ng, BG (author)
Freeze, HH (author)
Gabriel, M (author)
Russi, AHS (author)
Brick, L (author)
Kozenko, M (author)
Earl, DL (author)
Tham, E (author)
Karolinska Institutet
Nishimura, G (author)
Phillips, JA (author)
Gahl, WA (author)
Hamid, R (author)
Jackson, AP (author)
Grigelioniene, G (author)
Karolinska Institutet
Bober, MB (author)
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Elsevier BV, 2020
2020
English.
In: Genetics in medicine : official journal of the American College of Medical Genetics. - : Elsevier BV. - 1530-0366. ; 22:5, s. 857-866
  • Journal article (peer-reviewed)
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