about
Splitting and lumping in the nosology of XLMR.Coffin-Lowry syndrome.Deletion of the Coffin-Lowry syndrome gene Rsk2 in mice is associated with impaired spatial learning and reduced control of exploratory behavior.Coffin-Lowry syndrome: a 20-year follow-up and review of long-term outcomes.Syndromes of disordered chromatin remodeling.Unique X-linked mental retardation syndrome with fingertip arches and contractures linked to Xq21.31.Brief clinical report: early recognition of the Coffin-Lowry syndrome.Erk is essential for growth, differentiation, integrin expression, and cell function in human osteoblastic cells.Postmortem findings in the Coffin-Lowry Syndrome.Dopaminergic system dysregulation in the mrsk2_KO mouse, an animal model of the Coffin-Lowry syndrome.Mitral and tricuspid valve surgery for Coffin-Lowry syndrome.MRI and MRS of Coffin-Lowry syndrome: a case report.A new X-linked mental retardation syndrome.Pleiotropy in Coffin-Lowry syndrome: sensorineural hearing deficit and premature tooth loss as early manifestations.A Brazilian family with quadrupedal gait, severe mental retardation, coarse facial characteristics, and hirsutism.Coffin-Lowry syndrome: findings and dental treatment.A case of Coffin-Lowry syndrome with premature exfoliation of primary teeth.Crossover analysis in a British family suggests that Coffin-Lowry syndrome maps to a 3.4-cM interval in Xp22.Probable localisation of the Coffin-Lowry locus in Xp22.2-p22.1 by multipoint linkage analysis.The Coffin-Lowry syndrome. A study of two new index patients and their families.A family with the Coffin Lowry syndrome revisited: localization of CLS to Xp21-pter.Foramen magnum compression in Coffin-Lowry syndrome: A case report.The historical Coffin-Lowry syndrome family revisited: identification of two novel mutations of RPS6KA3 in three male patients.A rational approach to the child with mental retardation for the paediatrician
P2860
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P2860
description
article
@en
wetenschappelijk artikel
@nl
наукова стаття, опублікована в червні 1971
@uk
ലേഖനം
@ml
name
A New Dominant Gene Mental Retardation Syndrome
@en
A New Dominant Gene Mental Retardation Syndrome
@nl
type
label
A New Dominant Gene Mental Retardation Syndrome
@en
A New Dominant Gene Mental Retardation Syndrome
@nl
prefLabel
A New Dominant Gene Mental Retardation Syndrome
@en
A New Dominant Gene Mental Retardation Syndrome
@nl
P1476
A New Dominant Gene Mental Retardation Syndrome
@en
P2093
Brian Lowry
P356
10.1001/ARCHPEDI.1971.02100170078009
P577
1971-06-01T00:00:00Z