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Autosomal dominant transmission of isolated growth hormone deficiency in iris-dental dysplasia (Rieger's syndrome)

  • Published:1974-11 Issue:5 Volume:85 Page:644-648
  • ISSN:0022-3476
  • Container-title:The Journal of Pediatrics
  • language:en
  • Short-container-title:The Journal of Pediatrics

Author:

Sadeghi-Nejad Abdollah,Senior Boris

Publisher

Elsevier BV

Subject

Pediatrics, Perinatology and Child Health

Reference35 articles.

1. Congenitale Anomalien der Iris;Vossius;Klin. Monatsbl. Augenheilkd.,1883

2. Beiträge zur Kenntnis seltener Missbildungen der Iris;Rieger;Albrecht von Graefes Arch. Klin. Opthalmol.,1935

3. Rieger's syndrome;Feingold;Pediatrics,1969

4. Dysgenesis mesodermalis of the iris and the cornea. A study of Rieger's syndrome and Peter's anomaly;Alkemade,1969

5. Mendelian inheritance in man. Catalogs of autosomal dominant, autosomal recessive and X-linked phenotypes;McKusick,1971

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2. Pituitary Development and Organogenesis: Transcription Factors in Development and Disease;Masterclass in Neuroendocrinology;2020

3. Molecular Mechanisms Governing Embryonic Differentiation of Pituitary Somatotropes;Trends in Endocrinology & Metabolism;2018-07

4. The Rieger Syndrome: a Case Report with Unusual Dental Findings;Balkan Journal of Dental Medicine;2018-03-01

5. Anterior Segment Dysgenesis Syndromes;Practical Management of Pediatric Ocular Disorders and Strabismus;2016
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