Homozygous
WASHC4
variant in two sisters causes a syndromic phenotype defined by dysmorphisms, intellectual disability, profound developmental disorder, and skeletal muscle involvement
Keyword(s):
2001 ◽
Vol 11
(3)
◽
pp. 217-221
◽
Keyword(s):
2003 ◽
Vol 7
(6)
◽
pp. 401-406
◽
2017 ◽
1985 ◽
Vol 7
(6)
◽
pp. 585-589
◽