Further delineation of the 3-M syndrome with review of the literature.

Further delineation of the 3-M syndrome with review of the literature.

Item
http://www.wikidata.org/entity/Q39677026
Neuroblastoma amplified sequence gene is associated with a novel short stature syndrome characterised by optic nerve atrophy and Pelger-Huët anomalyDwarfism with gloomy face: a new syndrome with features of 3-M syndrome.Identification of mutations in CUL7 in 3-M syndrome.3M syndrome: a report of four cases in two familiesClinical, molecular and histopathological features of short stature syndrome with novel CUL7 mutation in Yakuts: new population isolate in Asia.Exploring the spectrum of 3-M syndrome, a primordial short stature disorder of disrupted ubiquitination.The 3-M syndrome: risk of intracerebral aneurysm?3-M syndrome and intracerebral aneurysms.3-M syndrome in two sisters.A large-scale mutation search reveals genetic heterogeneity in 3M syndrome.Is autosomal recessive Silver-Russel syndrome a separate entity or is it part of the 3-M syndrome spectrum?
P2860

Further delineation of the 3-M syndrome with review of the literature.

Item
http://www.wikidata.org/entity/Q39677026
description
1987 nî lūn-bûn
@nan
1987年の論文
@ja
1987年論文
@yue
1987年論文
@zh-hant
1987年論文
@zh-hk
1987年論文
@zh-mo
1987年論文
@zh-tw
1987年论文
@wuu
1987年论文
@zh
1987年论文
@zh-cn
name
Further delineation of the 3-M syndrome with review of the literature.
@en
Further delineation of the 3-M syndrome with review of the literature.
@nl
type
label
Further delineation of the 3-M syndrome with review of the literature.
@en
Further delineation of the 3-M syndrome with review of the literature.
@nl
prefLabel
Further delineation of the 3-M syndrome with review of the literature.
@en
Further delineation of the 3-M syndrome with review of the literature.
@nl
P1433
P1476
P2093
P2860
P304
P31
P356
P433
P478
P577
P698
P356
P1433
P1476
Further delineation of the 3-M syndrome with review of the literature.
@en
P2093
P2860
P304
P31
P356
P433
P478
P577
P698