A syndrome of congenital aplasia of the alae nasi, deafness, hypothyroidism, dwarfism, absent permanent teeth, and malabsorption
- 1 December 1971
- journal article
- Published by Elsevier in The Journal of Pediatrics
- Vol. 79 (6) , 982-987
- https://doi.org/10.1016/s0022-3476(71)80194-4
Abstract
No abstract availableThis publication has 6 references indexed in Scilit:
- Focal Dermal Hypoplasia SyndromeArchives of Dermatology, 1970
- Absorption of Oral Thyroxine in ManJournal of Clinical Endocrinology & Metabolism, 1968
- Otic Lesions and Congenital Hypothyroidism in the Developing Chick*Journal of Clinical Investigation, 1967
- Familial Syndrome Combining Deaf-Mutism, Stippled Epiphyses, Goiter and Abnormally High PBI: Possible Target Organ Refractoriness to Thyroid Hormone12Journal of Clinical Endocrinology & Metabolism, 1967
- Unusual case of XXY Klinefelter's syndrome with pancreatic insufficiency, hypothyroidism, deafness, chronic lung disease, dwarfism and microcephalyThe American Journal of Medicine, 1966
- Oculodentodigital dysplasiaThe Journal of Pediatrics, 1963