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Identification of a novel microdeletion causative of Nance-Horan syndrome.
Lopez Martinolich, Mariana; Northrup, Hope; Mancias, Pedro; Hillman, Paul; Rao, Kavya; Mowrey, Kate.
Affiliation
  • Lopez Martinolich M; Department of Pediatrics, Division of Medical Genetics, McGovern Medical School at the University of Texas Health Science Center at Houston (UTHealth Houston) and Children's Memorial Hermann Hospital, Houston, Texas, USA.
  • Northrup H; Department of Pediatrics, Division of Medical Genetics, McGovern Medical School at the University of Texas Health Science Center at Houston (UTHealth Houston) and Children's Memorial Hermann Hospital, Houston, Texas, USA.
  • Mancias P; Department of Pediatrics, Division of Child and Adolescent Neurology, McGovern Medical, School at the University of Texas Health Science Center at Houston (UTHealth Houston) and Children's Memorial Hermann Hospital, Houston, Texas, USA.
  • Hillman P; Department of Pediatrics, Division of Medical Genetics, McGovern Medical School at the University of Texas Health Science Center at Houston (UTHealth Houston) and Children's Memorial Hermann Hospital, Houston, Texas, USA.
  • Rao K; Department of Pediatrics, Division of Medical Genetics, McGovern Medical School at the University of Texas Health Science Center at Houston (UTHealth Houston) and Children's Memorial Hermann Hospital, Houston, Texas, USA.
  • Mowrey K; Department of Pediatrics, Division of Medical Genetics, McGovern Medical School at the University of Texas Health Science Center at Houston (UTHealth Houston) and Children's Memorial Hermann Hospital, Houston, Texas, USA.
Mol Genet Genomic Med ; 10(3): e1879, 2022 03.
Article in En | MEDLINE | ID: mdl-35122698
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Cataract / Glaucoma / Intellectual Disability Type of study: Diagnostic_studies / Prognostic_studies Limits: Humans / Male Language: En Journal: Mol Genet Genomic Med Year: 2022 Document type: Article Affiliation country: Estados Unidos Country of publication: Estados Unidos
Fulltext
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Cataract / Glaucoma / Intellectual Disability Type of study: Diagnostic_studies / Prognostic_studies Limits: Humans / Male Language: En Journal: Mol Genet Genomic Med Year: 2022 Document type: Article Affiliation country: Estados Unidos Country of publication: Estados Unidos