Disease: X-linked mental retardation and macro-orchidism
- (Over)correction of FMR1 deficiency with YAC transgenics: behavioral and physical features
- A family with mental retardation, variable macrocephaly and macro-orchidism, and linkage to Xq12-q21
- A mutation hot spot for nonspecific X-linked mental retardation in the MECP2 gene causes the PPM-X syndrome
- Adult fragile X syndrome. Clinico-neuropathologic findings
- Assessment of a clinical checklist in the diagnosis of fragile X syndrome in India
- Benign macro-orchidism in a pubescent boy
- Brief report: linkage between G6PD and fragile-X syndrome
- Central nervous system neoplasm in a young man with Martin-Bell syndrome--fra(X)-XLMR
- Changes in insulin-like growth factor signaling alter phenotypes in Fragile X Mice
- Expanding phenotype of p.Ala140Val mutation in MECP2 in a 4 generation family with X-linked intellectual disability and spasticity
- Familial X-linked mental retardation and fragile X chromosomes in two Swedish families
- Familial X-linked mental retardation syndrome associated with minor congenital anomalies, macro-orchidism, and fragile X-chromosome
- Familial X-linked mental retardation with a marker X chromosome and its relationship to macro-orchidism
- Familial X-linked mental retardation with an X chromosome abnormality and macro-orchidism
- Fragile X (Martin Bell) syndrome
- Fragile X and autistic mental retardation
- Fragile X chromosome and X-linked mental retardation
- Fragile X chromosome and X-linked mental retardation (author's transl)
- Fragile X syndrome: clinical and molecular genetics correlations
- Fragile X syndrome. Clinical and cytogenetic studies
- Fragile X-linked mental retardation of macro-orchidism
- Fragile X-linked mental retardation: the Martin-Bell syndrome
- Fragile X-linked mental retardation. A survey of 65 patients with mental retardation of unknown origin
- Fragile X-syndrome and mental retardation
- Fragile-X syndrome ascertained by the presence of macro-orchidism in a 5-month-old infant
- Genetic removal of p70 S6 kinase 1 corrects molecular, synaptic, and behavioral phenotypes in fragile X syndrome mice
- Gonadal function in men with the Martin-Bell (fragile-X) syndrome
- Heterozygous expression of X-linked mental retardation and X-chromosome marker fra(X)(q27)
- High resolution ultrasound of macro-orchidism in mental retardation
- Incidence of macro-orchidism in patients with mental retardation: according to evaluation criteria
- Knockout mouse model for Fxr2: a model for mental retardation
- Learning disabilities and attentional problems in boys with the fragile X syndrome
- Molecular cytogenetics of fragile X syndrome
- Molecular diagnosis of fragile X syndrome
- Molecular pathology of the fragile X syndrome
- Neuroanatomy of the fragile X knockout mouse brain studied using in vivo high resolution magnetic resonance imaging
- Neurofibromatosis and fragile-X syndrome in the same patient
- Neurological findings in patients with the fragile-X syndrome
- Neuropsychological studies in families with fragile-X negative X-linked mental retardation
- Nonspecific X-linked mental retardation I: a review with information from 24 new families
- Orthopaedic aspects of fragile-X syndrome
- Preimplantation diagnosis for fragile X syndrome based on the detection of the non-expanded paternal and maternal CGG
- Prevalence and clinical characteristics of fragile X syndrome at child development clinic, Ramathibodi Hospital
- Prevalence of the fragile X syndrome in an institution for the mentally handicapped
- Proteomic Profiling of Brain and Testis Reveals the Diverse Changes in Ribosomal Proteins in fmr1 Knockout Mice
- Race distribution in X-linked mental retardation with macro-orchidism and fragile site in Xq
- Role of Taurine in Testicular Function in the Fragile x Mouse
- Screening for fragile X syndrome
- Screening for the fragile X syndrome among the mentally retarded: a clinical study. The Collaborative Fragile X Study Group
- Screening of mentally retarded males for macro-orchidism and the fragile X chromosome
- Significance of phenotypic and chromosomal abnormalities in X-linked mental retardation (Martin-Bell or Renpenning syndrome)
- Spatial learning, contextual fear conditioning and conditioned emotional response in Fmr1 knockout mice
- The clinical phenotype in institutionalised adult males with X-linked mental retardation (XLMR)
- The fragile X syndrome
- The fragile X syndrome (Martin-Bell syndrome). Clinical and cytogenetic findings in 16 prepubertal boys and in 4 of their 5 families
- The fragile X syndrome II: preliminary data on growth and development in males
- True precocious puberty in a girl with the fragile X syndrome
- Variable expression of clinical features of Martin Bell syndrome in younger patients
- X chromosome-linked mental retardation with fragile X chromosome and macro-orchidism
- X-linked mental retardation associated with macro-orchidism
- X-linked mental retardation with macro-orchidism and marker X chromosomes
- X-linked mental retardation with macro-orchidism and marker-X chromosomes
- X-linked mental retardation with macro-orchidism and the fragile site at Xq 27 or 28
- X-linked mental retardation, macro-orchidism, and the Xq27 fragile site
- X-linked mental retardation: a study of 7 families
- X-linked mental retardation: Renpenning revisited