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Format : Academic Journals Format : Academic Journals Subject : adhd Subject : conners teacher rating scale Subject : fragile x syndrome Filter by : Subject
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Academic Journal

The Human Genome Project--threat or promise?

Subjects: Human Genome Project*; Fragile X Syndrome/Fragile X Syndrome/Fragile X Syndrome/*genetics ; Molecular Biology/Molecular Biology/Molecular Biology/*trends

  • Source: Journal of intellectual disability research : JIDR [J Intellect Disabil Res] 2003 Oct; Vol. 47 (Pt 7), pp. 505-8.Publisher: Blackwell Scientific Publications on behalf of the Royal Society for Mentally Handicapped Children and Adults Country of Publication: England NLM ID:

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Editorial & Opinion

Fragile X gene.

Subjects: Genes* ; Human Genome Project*; Fragile X Syndrome/Fragile X Syndrome/Fragile X Syndrome/*genetics

  • Source: Science (New York, N.Y.) [Science] 1991 Sep 27; Vol. 253 (5027), pp. 1467.Publisher: American Association for the Advancement of Science Country of Publication: United States NLM ID: 0404511 Publication Model: Print Cited Medium:

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Academic Journal

The Current State of Charcot–Marie–Tooth Disease Treatment.

Subjects: CHARCOT-Marie-Tooth disease; THERAPEUTICS; GENE therapy

  • Source: Genes; Jul2023, Vol. 14 Issue 7, p1391, 17p

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Academic Journal

3q29 microduplication syndrome: New evidence for the refinement of the critical region.

Subjects: FRAGILE X syndrome; NUCLEOTIDE sequencing; AUTISM spectrum disorders

  • Source: Molecular Genetics & Genomic Medicine; Apr2023, Vol. 11 Issue 4, p1-7, 7p

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Academic Journal

Annual Research Review: The (epi)genetics of neurodevelopmental disorders in the era of whole-genome sequencing - unveiling the dark matter.

Subjects: ATTENTION-deficit hyperactivity disorder; AUTISM; DEVELOPMENTAL disabilities

  • Source: Journal of Child Psychology & Psychiatry. Mar2015, Vol. 56 Issue 3, p278-295. 18p.

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Academic Journal

Comment on Herring et al. The Use of "Retardation" in FRAXA, FMRP, FMR1 and Other Designations. Cells 2022, 11 , 1044.

Subjects: HUMAN genome; ATLANTIC herring; FRAGILE X syndrome

  • Source: Cells (2073-4409); Jun2022, Vol. 11 Issue 12, p1937-N.PAG, 5p

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Academic Journal

The Use of "Retardation" in FRAXA, FMRP, FMR1 and Other Designations.

Subjects: HUMAN genome; FRAGILE X syndrome

  • Source: Cells (2073-4409); Mar2022, Vol. 11 Issue 6, p1044, 7p

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Academic Journal

Common Threads: Aphidicolin-Inducible and Folate-Sensitive Fragile Sites in the Human Genome.

Subjects: HUMAN genome; DNA synthesis; FRAGILE X syndrome

  • Source: Frontiers in Genetics; 9/8/2021, Vol. 12, p1-8, 8p

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Academic Journal

Abundancy of polymorphic CGG repeats in the human genome suggest a broad involvement in neurological disease.

Subjects: NEUROLOGICAL disorders; GENETIC polymorphisms; HUMAN genome

  • Source: Scientific Reports; 1/28/2021, Vol. 11 Issue 1, p1-11, 11p

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Academic Journal

Comprehensive analysis of the transcriptional landscape of the human FMR1 gene reveals two new long noncoding RNAs differentially expressed in Fragile X syndrome and Fragile X-associated tremor/ataxia syndrome.

Subjects: GENETIC transcription; HUMAN genome; FRAGILE X syndrome

  • Source: Human Genetics; Jan2014, Vol. 133 Issue 1, p59-67, 9p

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  • 1-10 of  42 results for ""HUMAN genome""