Related Experiment Videos

Idiopathic hypoparathyroidism presenting with seizures during infancy: X-linked recessive inheritance in a large

M P Whyte, V V Weldon

The Journal of Pediatrics

|October 1, 1981

Abstract

No abstract available in PubMed .

Related Concept Videos

Articles linked to this work by shared authors, journal, and citation graph.

Periodontal Defects in the A116T Knock-in Murine Model of Odontohypophosphatasia.

Journal of dental research·2015

Enzyme replacement therapy prevents dental defects in a model of hypophosphatasia.

Journal of dental research·2011

Alendronate for the treatment of pediatric osteogenesis imperfecta: a randomized placebo-controlled study.

The Journal of clinical endocrinology and metabolism·2010

Cementum and dentin in hypophosphatasia.

Journal of dental research·2005

Preonset studies of spondyloepiphyseal dysplasia tarda caused by a novel 2-base pair deletion in SEDL encoding sedlin.

Journal of bone and mineral research : the official journal of the American Society for Bone and Mineral Research·2002

Clinical delineation and localization to chromosome 9p13.3-p12 of a unique dominant disorder in four families: hereditary inclusion body myopathy, Paget disease of bone, and frontotemporal dementia.

Molecular genetics and metabolism·2001

See all related articles