The syndrome of retinal pigmentary degeneration, microcephaly, and severe mental retardation (Mirhosseini-Holmes-Walton syndrome): report of two patients.
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Cohen syndrome: essential features, natural history, and heterogeneityAllelic heterogeneity in the COH1 gene explains clinical variability in Cohen syndrome.A syndrome of severe mental retardation, spasticity, and tapetoretinal degeneration linked to chromosome 15q24Microcephaly with chorioretinopathy. A report of two dominant families and three sporadic cases.Lissencephaly and mild cerebellar vermis hypoplasia in a case of microcephaly and chorioretinal dysplasia.Feedback regulation of RTK signaling in development.
P2860
The syndrome of retinal pigmentary degeneration, microcephaly, and severe mental retardation (Mirhosseini-Holmes-Walton syndrome): report of two patients.
description
1985 nî lūn-bûn
@nan
1985年の論文
@ja
1985年論文
@yue
1985年論文
@zh-hant
1985年論文
@zh-hk
1985年論文
@zh-mo
1985年論文
@zh-tw
1985年论文
@wuu
1985年论文
@zh
1985年论文
@zh-cn
name
The syndrome of retinal pigmen ...... rome): report of two patients.
@en
type
label
The syndrome of retinal pigmen ...... rome): report of two patients.
@en
prefLabel
The syndrome of retinal pigmen ...... rome): report of two patients.
@en
P2093
P356
P1476
The syndrome of retinal pigmen ...... rome): report of two patients.
@en
P2093
Paskulin GA
Vallandro C
P304
P356
10.1002/AJMG.1320220202
P577
1985-10-01T00:00:00Z