Progressive facial hematiatrophy (Romberg syndrome) and uveal coloboma.
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Atrophy↗
Biomedical subjects
M JEQUIER
Publications and source records attributed to M JEQUIER.
[Differential diagnosis of arm pains].
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Arm↗
[Dominant heredity of progressive muscular dystrophy in family in Vaud].
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Heredity↗
[Pseudotumoral encephalitides; an anatomopathological study of five cases].
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Brain↗
[Therapeutic effects of cytochrome C in myopathies].
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Cytochromes↗
[Oto-neuro-ophthalmological complications in myeloid leukemia in subjects with latent familial cranial abnormalities].
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Craniofacial Abnormalities↗
[Developmental disorders in the nervous system and sensory organs].
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Child↗
[Myotonic dystrophy and diabetes mellitus].
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Diabetes Mellitus↗
[Natiform skull].
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Craniofacial Abnormalities↗
[Myotonic dystrophy and cranial hyperostosis].
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Bone and Bones↗
[Familial paralytic keratitis and hereditary multiple nerve degeneration in the same population].
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Humans↗