Pages that link to "Q52121182"

The following pages link to X-linked mental retardation and-or hydrocephalus (Q52121182):

Displaying 20 items.

• Possible linkage between Xg and the locus for a gene causing mental retardation with or without hydrocephalus (Q33585520) (← links)
• X-linked mental retardation. (Q33585997) (← links)
• X-Y translocation in a retarded phenotypic male. Clinical, cytogenetic, biochemical, and serogenetic studies (Q33588425) (← links)
• MASA syndrome (a form of complicated spastic paraplegia) and X linked hydrocephalus: variable expression of the same mutation at Xq28? Call for families (Q33593878) (← links)
• Non-specific X linked mental retardation (Q33597050) (← links)
• A family study of hydrocephalus resulting from aqueduct stenosis (Q33668771) (← links)
• X linked hydrocephalus: a survey of a 20 year period in Victoria, Australia (Q33672323) (← links)
• Fried syndrome is a distinct X linked mental retardation syndrome mapping to Xp22. (Q33679076) (← links)
• X linked hydrocephalus and MASA syndrome (Q33683093) (← links)
• A modifier locus on chromosome 5 contributes to L1 cell adhesion molecule X-linked hydrocephalus in mice (Q33824335) (← links)
• A new form of X-linked mental retardation with growth retardation, deafness, and microgenitalism. (Q34246089) (← links)
• Infantile hydrocephalus: a review of epidemiology, classification and causes (Q35101052) (← links)
• Further localization of X-linked hydrocephalus in the chromosomal region Xq28 (Q35195648) (← links)
• AP1S2 is mutated in X-linked Dandy-Walker malformation with intellectual disability, basal ganglia disease and seizures (Pettigrew syndrome). (Q37585836) (← links)
• Nonspecific X-linked mental retardation--a review (Q40252273) (← links)
• The site of a missense mutation in the extracellular Ig or FN domains of L1CAM influences infant mortality and the severity of X linked hydrocephalus (Q42056967) (← links)
• Mutations in the AP1S2 gene encoding the sigma 2 subunit of the adaptor protein 1 complex are associated with syndromic X-linked mental retardation with hydrocephalus and calcifications in basal ganglia (Q42566633) (← links)
• X-linked mental retardation: in pursuit of a gene map. (Q43147044) (← links)
• Adult fragile X syndrome. Clinico-neuropathologic findings (Q48545759) (← links)
• Malformations among the X-linked intellectual disability syndromes. (Q54684565) (← links)