Results 171 to 180 of about 34,300 (180)
[46,XY disorder of sex development caused by <i>PPP1R12A</i> gene variants: a case report]. [PDF]
Su W +6 more
europepmc +1 more source
[Research progresses in gene therapy for hepatolenticular degeneration]. [PDF]
Chen G +5 more
europepmc +1 more source
[Type II Leydig cell hypoplasia caused by LHCGR gene mutation: a case report]. [PDF]
Jin KX +6 more
europepmc +1 more source
[Clinical and genetic features of 5 neonates with centronuclear myopathy caused by MTM1 gene variation]. [PDF]
Xie T +7 more
europepmc +1 more source
[Cohen syndrome in a child caused by compound heterozygous variants in VPS13B gene]. [PDF]
Mei X +6 more
europepmc +1 more source
[The role and molecular mechanism of transcription factor EB and its target genes in multiple myeloma treatment with bortezomib]. [PDF]
Zhang RJ +8 more
europepmc +1 more source

