|
Copper deficiency, familial benign
|
C535468 |
|
|
UL135 protein, human herpesvirus 5
|
C000600444 |
|
|
Coproporphyria
|
C535469 |
|
|
UL136 protein, human herpesvirus 5
|
C000600445 |
|
|
WTX protein, mouse
|
C000600446 |
|
|
SNX20 protein, mouse
|
C000600447 |
|
|
SNX21 protein, mouse
|
C000600448 |
|
|
Corneal dystrophy, gelatinous drop-like
|
C535480 |
|
|
Fraser Jequier Chen syndrome
|
C535481 |
|
|
Freeman-Sheldon syndrome
|
C535483 |
|
|
13q deletion syndrome
|
C535484 |
|
|
Chromosome 13q trisomy
|
C535485 |
|
|
Chromosome 13q-mosaicism
|
C535486 |
|
|
Ring Chromosome 14 Syndrome
|
C535487 |
|
|
1,3,5,7-tetramethyl-8-(N-hydroxysuccinimidylbutyric ester)difluoroboradiaza-s-indacene
|
C560400 |
|
|
nitrocefin
|
C021720 |
|
|
21-nor-18,27-dimethyl-1,2,3-trihydroxy-25-spirost-4-en-19-oic acid
|
C560401 |
|
|
A 967079
|
C560402 |
|
|
oligo(dT)-cellulose
|
C021722 |
|
|
2,7-bis(1-hydroxyethyl-4-vinylpyridinium iodine)-N-ethylcarbazole
|
C560403 |
|
