A SHORTENED AUTOMATED PROCEDURE FOR THE DETERMINATION OF ALKALINE PHOSPHATASE.
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Alkaline Phosphatase↗
Biomedical subjects
M COLLIER
Publications and source records attributed to M COLLIER.
[HEREDO-FAMILIAL NATURE OF PREDESCEMETIC PUNCTIFORM DYSTROPHY].
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Child↗
[Corneal dystrophies, nevi and pigmentation disorders in genodermatoses. (Keratosis pilaris rubra and pityriasis rubra pilaris].
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Abnormalities, Multiple↗
[THE NEVUS OF THE TAIL OF THE EYEBROW AND ITS PATHOLOGICAL ASSOCIATIONS].
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Adolescent↗
[THE WHITE FORELOCK AND MYOPIA AS "INDICATOR" FACTORS OF THE WAARDENBURG-KLEIN SYNDROME].
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Child↗
[CORNEAL DYSTROPHIES, NEVI, AND PIGMENTATION DISORDERS IN GENODERMATOSES (KERATOSIS PILARIS RUBRA AND PITYRIASIS RUBRA PILARIS)].
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Abnormalities, Multiple↗
[UVEITIS AND MULTIPLE SCLEROSIS].
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Adolescent↗
[Corneal dystrophy of the Reis-Bucklers type and congenital anomalies of the anterior segment].
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Cornea↗
[Posterior marginal dysplasia of the cornea in the framework of skeletal and ectodermal anomalies].
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Bone Diseases↗
[Presenile macular degeneration, partial albinism and pachydermoperiostosis].
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Albinism↗
[A rare sequel of ophthalmic zona: fatty dystrophy of the cornea].
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Cornea↗
[Annular dystrophy of the corneal endothelium, posterior keratoconus and cylindrical protrusion of the cornea].
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Cornea↗
[Atrophia gyrata choroideae et retinae and its syndromic relations].
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Choroid↗
[Bowman's white ring (Coats' ring)].
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Corneal Dystrophies, Hereditary↗
[Changes in the crystalline lens of patients with psoriasis].
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Cataract↗
[Congenital and degenerative anomalies of the fundus oculi in patients with certain spinal malformations and deteriorations].
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Connective Tissue Diseases↗
[Modifications of the crystalline in psoriasis patients].
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Cataract↗