A large interstitial 11q deletion with isolated mild intellectual disability: review of the literature for genotype-phenotype correlation.

Lallar, Meenakshi; Srivastava, Priyanka; Phadke, Shubha R

Lallar, Meenakshi; Srivastava, Priyanka; Phadke, Shubha R.

Affiliation

Lallar M; Department of Medical Genetics, Sanjay Gandhi Post Graduate Institute of Medical Sciences, Lucknow, India.

Clin Dysmorphol ; 27(4): 142-144, 2018 Oct.

Article in En | MEDLINE | ID: mdl-29847353

Subject(s)

Intellectual Disability/genetics; Smith-Magenis Syndrome/genetics; Smith-Magenis Syndrome/metabolism; Child; Chromosome Deletion; Chromosomes, Human, Pair 11/genetics; Chromosomes, Human, Pair 17/genetics; Chromosomes, Human, Pair 17/metabolism; Genetic Association Studies; Humans; Male; Phenotype

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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Smith-Magenis Syndrome / Intellectual Disability Type of study: Prognostic_studies Limits: Child / Humans / Male Language: En Journal: Clin Dysmorphol Journal subject: TERATOLOGIA Year: 2018 Document type: Article Affiliation country: India Country of publication: United kingdom

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