Clinical anophthalmia, dextrocardia, and skeletal anomalies in an infant born to consanguineous parents
Clinical anophthalmia; unusual facies (sloping forehead, prominent nasal root and bridge, large pinnae, mild micrognathia); dextrocardia; vertebral fusion defects; supernumerary ribs; and normal growth and development in infancy.
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Veröffentlicht in: | American journal of medical genetics 1990-10, Vol.37 (2), p.178-181 |
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container_title | American journal of medical genetics |
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creator | Aughton, David J. |
description | Clinical anophthalmia; unusual facies (sloping forehead, prominent nasal root and bridge, large pinnae, mild micrognathia); dextrocardia; vertebral fusion defects; supernumerary ribs; and normal growth and development in infancy. |
doi_str_mv | 10.1002/ajmg.1320370204 |
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source | MEDLINE; Alma/SFX Local Collection |
subjects | Abnormalities, Multiple - genetics Anophthalmos - genetics Biological and medical sciences Bone and Bones - abnormalities Complex syndromes Consanguinity Dextrocardia - genetics Face - abnormalities Humans Infant, Newborn Male Medical genetics Medical sciences multiple congenital anomalies Ribs - abnormalities Spine - abnormalities Syndrome vertebral/ rib anomalies |
title | Clinical anophthalmia, dextrocardia, and skeletal anomalies in an infant born to consanguineous parents |
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