## Abstract ## BACKGROUND JohnsonβMcMillin syndrome (JMS) is a rare neuroectodermal disorder characterized by alopecia, ear malformations, conductive hearing loss, anosmia/hyposmia, and hypogonadotropic hypogonadism. It is inherited in an autosomal dominant manner; however, the causative gene has
Juberg-Hayward syndrome: Report of a new patient with severe phenotype and novel clinical features
β Scribed by Hedera, Peter ;Innis, Jeffrey W.
- Publisher
- John Wiley and Sons
- Year
- 2003
- Tongue
- English
- Weight
- 106 KB
- Volume
- 122A
- Category
- Article
- ISSN
- 0148-7299
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The centronuclear myopathies are a clinically and genetically heterogeneous group of disorders which share similar histological features on muscle biopsy. The familial cases have been classified genetically as X-linked or autosomal in inheritance. The autosomal forms usually have a later onset and m
## Background: During embryonal development primitive hematopoiesis can be observed first in the yolk sac, in which both hematopoietic and endothelial cells are derived from a common precursor, the hemangioblast. whether cells with this dual differentiation potential persist during postnatal life i