Search details
1.
Inflammatory facioscapulohumeral muscular dystrophy type 2 in 18p deletion syndrome.
Am J Med Genet A
; 176(8): 1760-1763, 2018 08.
Article
in English
| MEDLINE | ID: mdl-30055030
2.
FSHD1 and FSHD2 form a disease continuum.
Neurology
; 92(19): e2273-e2285, 2019 05 07.
Article
in English
| MEDLINE | ID: mdl-30979860
Results
1 -
2
de 2
1
Next >
>>