about
Mutation analysis of the RSK2 gene in Coffin-Lowry patients: extensive allelic heterogeneity and a high rate of de novo mutationsThe Coffin-Lowry syndrome."Cataplexy" and muscle ultrasound abnormalities in Coffin-Lowry syndromeMitochondrial DNA mutations and pathogenicityCoffin-Lowry syndrome: clinical and molecular features.Coffin-Lowry syndrome: a 20-year follow-up and review of long-term outcomes.Rapid immunoblot and kinase assay tests for a syndromal form of X linked mental retardation: Coffin-Lowry syndrome"Cataplexy" in Coffin-Lowry syndromePostmortem findings in the Coffin-Lowry Syndrome.Coffin-Lowry syndrome: findings and dental treatment.
P2860
Q24539742-7001D388-E887-4D86-8157-3AB17843DFC0Q33676721-85541E43-A09A-4914-B3FD-F829B7F78981Q33680152-1CC72F27-8323-412D-9A54-B7DB7E29904AQ33681202-01373F27-7A44-4545-B8D9-8DA52E941EEBQ34152932-0B31C950-272E-43F6-8606-F44E6584D13DQ34811039-02916FFF-7113-4D7A-9DEE-B853AEE3BBDCQ41818950-CEA6B88D-CA4D-4133-B538-42096FCDCD07Q42666495-9769A185-409C-4469-B80F-156A1235E8E0Q45961186-3076AA25-58C2-4315-897D-37E86EB0D926Q51907719-F352DECC-9077-45F4-9873-CA579030E34B
P2860
description
1977 nî lūn-bûn
@nan
1977年の論文
@ja
1977年学术文章
@wuu
1977年学术文章
@zh
1977年学术文章
@zh-cn
1977年学术文章
@zh-hans
1977年学术文章
@zh-my
1977年学术文章
@zh-sg
1977年學術文章
@yue
1977年學術文章
@zh-hant
name
The Coffin syndrome.
@en
type
label
The Coffin syndrome.
@en
prefLabel
The Coffin syndrome.
@en
P2093
P356
P1433
P1476
The Coffin syndrome.
@en
P2093
H Van den Berghe
P2888
P304
P356
10.1007/BF00446276
P577
1977-05-01T00:00:00Z