Apparent association of mental retardation and specific patterns of deletions screened with probes cf56a and cf23a in Duchenne muscular dystrophy.

No abstract is available for this paper.

• Publication year

  1991

• Venue

  American journal of medical genetics

• Publication date

  1991-06-15

• Fields of study

  Biology, Medicine

• Identifiers
  DOI 10.1002/AJMG.1320390414PMID 1877622
• External record

  Open on Semantic Scholar

• Source metadata

  Semantic Scholar, PubMed

• No claims are published for this paper.

• No concepts are published for this paper.

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  1990cited by this paper
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  1990cited by this paper
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  1989cited by this paper
• Correlation of clinical and deletion data in Duchenne and Becker muscular dystrophy.

  1989cited by this paper
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  1989cited by this paper
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  1989cited by this paper
• Alternative splicing of human dystrophin mRNA generates isoforms at the carboxy terminus

  1989cited by this paper
• Duchenne muscular dystrophy: the gene and the protein.

  1989cited by this paper
• Similarity of IQs of siblings with Duchenne progressive muscular dystrophy.

  1989cited by this paper
• Gene deletions in X-linked muscular dystrophy.

  1989cited by this paper
• Clinical concepts of Duchenne muscular dystrophy. The impact of molecular genetics.

  1988cited by this paper
• Expression of the putative Duchenne muscular dystrophy gene in differentiated myogenic cell cultures and in the brain

  1988cited by this paper
• Further studies of gene deletions that cause Duchenne and Becker muscular dystrophies.

  1988cited by this paper
• Cell and fiber-type distribution of dystrophin.

  1988cited by this paper
• Deletions of fetal and adult muscle cDNA in Duchenne and Becker muscular dystrophy patients.

  1987cited by this paper
• Preferential deletion of exons in Duchenne and Becker muscular dystrophies

  1987cited by this paper
• Phenotypic features of patients with congenital adrenal hypoplasia and glycerol kinase deficiency.

  1987cited by this paper
• Duchenne muscular dystrophy due to familial Xp21 deletion detectable by DNA analysis and flow cytometry

  1986cited by this paper
• Investigation on genetic heterogeneity in Duchenne muscular dystrophy.

  1986cited by this paper
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  1985cited by this paper
• A technique for radiolabeling DNA restriction endonuclease fragments to high specific activity.

  1983cited by this paper
• Analysis of human Y-chromosome-specific reiterated DNA in chromosome variants.

  1977cited by this paper
• Detection of specific sequences among DNA fragments separated by gel electrophoresis.

  1975cited by this paper
• Mental retardation in patients with Duchenne progressive muscular dystrophy.

  1971cited by this paper
• The Genetic Relationship of Progressive Muscular Dystrophy (Duchenne Type) and Mental Retardation

  1968cited by this paper
• Intellectual Impairment in Muscular Dystrophy

  1965cited by this paper
• Mental retardation in association with progressive dystrophy.

  1960cited by this paper
• Mental Retardation in Association with Progressive Muscular Dystrophy

  1960cited by this paper

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  2026cites this paper
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  2023cites this paper
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  2018cites this paper
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  2017cites this paper
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  2009cites this paper
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  2009cites this paper
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  2007cites this paper
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  2005cites this paper
• Mental Retardation

  2005cites this paper
• Brain function in Duchenne muscular dystrophy.

  2002cites this paper
• [Duchenne's and Becker's muscular dystrophy: analysis of phenotype-genotype correlation in 28 patients] ].

  2002cites this paper
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• Duchenne's/Becker's muscular dystrophy: Analysis of genotype-feno-type correlation in 28 patients

  2002cites this paper
• Detección de Portadoras de Distrofia Muscular Duchenne/Becker a través del Análisis de Loci STRs Ligados al Gen de la Distrofina en Familias Venezolanas

  2002cites this paper
• A biologia molecular contribuindo para a compreensão e a prevenção das doenças hereditárias

  2002cites this paper
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  2001cites this paper
• Severe cognitive impairment in DMD: obvious clinical evidence for Dp71 isoform point mutations screening

  2000cites this paper
• Brain dystrophin, neurogenetics and mental retardation.

  2000cites this paper
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  2000cites this paper
• Severe cognitive impairment in DMD: obvious clinical indication for Dp71 isoform point mutation screening.

  2000cites this paper
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  2000cites this paper
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  2000cites this paper
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  1999cites this paper
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  1999cites this paper
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  1998cites this paper
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  1998cites this paper
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  1998cites this paper
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  1998cites this paper
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  1998cites this paper
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  1998cites this paper
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  1998cites this paper
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  1998cites this paper
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  1996cites this paper
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  1996cites this paper
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  1995cites this paper
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  1995cites this paper
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  1995cites this paper
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  1995cites this paper
• 6 Dystrophin, Its Gene, and the Dystrophinopathies

  1995cites this paper
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  1994cites this paper
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  1993cites this paper
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  1993cites this paper
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  1993cites this paper
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  1993cites this paper
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  1993cites this paper
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  1993cites this paper
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  1993cites this paper
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  1993cites this paper
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  1993cites this paper
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  1993cites this paper
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  1993cites this paper
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  1993cites this paper
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  1993cites this paper
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  1992cites this paper
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  1992cites this paper
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  1992cites this paper
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  1992cites this paper
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  1992cites this paper
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  1992cites this paper
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  1991cites this paper
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  1991cites this paper