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Archives of Otolaryngology - Head and Neck Surgery, 1970
An unusual case of long-standing pseudomembranous inflammation resulted in complete palatalpharyngeal fusion. Extensive studies for diphtheria, fungi, tuberculosis, carcinoma, pemphigus, and upper respiratory scleroma failed to identify the cause.
A S, Miller, R D, Harwick, P A, Pullon
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An unusual case of long-standing pseudomembranous inflammation resulted in complete palatalpharyngeal fusion. Extensive studies for diphtheria, fungi, tuberculosis, carcinoma, pemphigus, and upper respiratory scleroma failed to identify the cause.
A S, Miller, R D, Harwick, P A, Pullon
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The Indian Journal of Pediatrics, 1970
A female child showed features of deafness, characteristic facies and a generalized bone dysplasia, and was diagnosed to have the “oto-palatal-digital syndrome”. The literature is briefly reviewed.
S D, Singh, M S, Diwedi, M, Irani
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A female child showed features of deafness, characteristic facies and a generalized bone dysplasia, and was diagnosed to have the “oto-palatal-digital syndrome”. The literature is briefly reviewed.
S D, Singh, M S, Diwedi, M, Irani
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The oto-palato-digital syndrome
The Journal of Laryngology & Otology, 1976A boy aged ten years with oto-palato-digital syndrome is discussed. Because of severe conductive hearing loss tympanotomy was performed and abnormal poorly mobile ossicles were found. Stapedectomy was performed without improvement of hearing.
L, Podoshin, H S, Heymans, M, Fradis
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Archives of Pediatrics & Adolescent Medicine, 1967
To the Editor .—With regard to our paper (Amer J Dis Child113:214-221, 1967), entitled "Oto-Palato-Digital Syndrome" we have seen another case in a boy who also had identical facies and in the Journal of Medical Genetics 3:17-22, 1966, there appeared to be four other cases reported in boys. This would clearly indicate that this syndrome is inherited as
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To the Editor .—With regard to our paper (Amer J Dis Child113:214-221, 1967), entitled "Oto-Palato-Digital Syndrome" we have seen another case in a boy who also had identical facies and in the Journal of Medical Genetics 3:17-22, 1966, there appeared to be four other cases reported in boys. This would clearly indicate that this syndrome is inherited as
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INHERITANCE OF THE OTO-PALATO-DIGITAL SYNDROME
Archives of Pediatrics & Adolescent Medicine, 1970To the Editor .—Dudding et al 1 in 1967 reported a family with multiple defects and suggested it be called the oto-palato-digital syndrome. In the sibship described there were three affected male subjects. It was suggested that the entity was probably autosomal recessive but could be X-linked.
G, Turner, R J, Gorlin
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