Matches in Nanopublications for { ?s ?p "[Hypoparathyroidism-retardation-dysmorphism (HRD) or Sanjad-Sakati syndrome (SSS) (OMIM 241410) is a rare autosomal recessive (AR) inherited condition, characterized by congenital hypoparathyroidism (hypoPTH), retardation, seizures, and a typical facial dysmorphism, consisting of prominent forehead, deep-set eyes, and abnormal external ears.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }
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- NP630826.RAC_xYFnFyDikFIfB0FuoeRdoUdVhq2Dw48GGkamlPVzE130_assertion description "[Hypoparathyroidism-retardation-dysmorphism (HRD) or Sanjad-Sakati syndrome (SSS) (OMIM 241410) is a rare autosomal recessive (AR) inherited condition, characterized by congenital hypoparathyroidism (hypoPTH), retardation, seizures, and a typical facial dysmorphism, consisting of prominent forehead, deep-set eyes, and abnormal external ears.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP630826.RAC_xYFnFyDikFIfB0FuoeRdoUdVhq2Dw48GGkamlPVzE130_provenance.
- NP615340.RAegpoh9u2AMaaHYFYADM_8bqtly3sUHXRiFaO8W1ljvk130_assertion description "[Hypoparathyroidism-retardation-dysmorphism (HRD) or Sanjad-Sakati syndrome (SSS) (OMIM 241410) is a rare autosomal recessive (AR) inherited condition, characterized by congenital hypoparathyroidism (hypoPTH), retardation, seizures, and a typical facial dysmorphism, consisting of prominent forehead, deep-set eyes, and abnormal external ears.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP615340.RAegpoh9u2AMaaHYFYADM_8bqtly3sUHXRiFaO8W1ljvk130_provenance.
- NP221244.RAh5-RF6eyh4kL8H33YA6dYebVih0U8piqR89gP6DoWzk130_assertion description "[Hypoparathyroidism-retardation-dysmorphism (HRD) or Sanjad-Sakati syndrome (SSS) (OMIM 241410) is a rare autosomal recessive (AR) inherited condition, characterized by congenital hypoparathyroidism (hypoPTH), retardation, seizures, and a typical facial dysmorphism, consisting of prominent forehead, deep-set eyes, and abnormal external ears.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP221244.RAh5-RF6eyh4kL8H33YA6dYebVih0U8piqR89gP6DoWzk130_provenance.
- NP794508.RArTdMcE6bqLnP1HvYLXNet_hhyjVaeqAWxEAA5QsDgGU130_assertion description "[Hypoparathyroidism-retardation-dysmorphism (HRD) or Sanjad-Sakati syndrome (SSS) (OMIM 241410) is a rare autosomal recessive (AR) inherited condition, characterized by congenital hypoparathyroidism (hypoPTH), retardation, seizures, and a typical facial dysmorphism, consisting of prominent forehead, deep-set eyes, and abnormal external ears.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP794508.RArTdMcE6bqLnP1HvYLXNet_hhyjVaeqAWxEAA5QsDgGU130_provenance.
- NP682861.RA32hBKlCQwwNsV47Hxj8N4eJQJBDIuTv6zDXrd0UeEro130_assertion description "[Hypoparathyroidism-retardation-dysmorphism (HRD) or Sanjad-Sakati syndrome (SSS) (OMIM 241410) is a rare autosomal recessive (AR) inherited condition, characterized by congenital hypoparathyroidism (hypoPTH), retardation, seizures, and a typical facial dysmorphism, consisting of prominent forehead, deep-set eyes, and abnormal external ears.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP682861.RA32hBKlCQwwNsV47Hxj8N4eJQJBDIuTv6zDXrd0UeEro130_provenance.