The philosophy and practice of screening for inherited diseases von Komrower, G M

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Maternal diabetes and congenital malformation von Komrower, G M

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Growth and skeletal maturation in congenital adrenal hyperplasia. Review of 20 cases von Bailey, C C, Komrower, G M

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Phenylketonuria. Some current problems von Komrower, G M

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Membership of the JCC von Komrower, G M

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Detection of heterozygotes for homocystinuria. Study of sulphur-containing amino acids in plasma and urine after L-methionine loading von Sardharwalla, I B, Fowler, B, Robins, A J, Komrower, G M

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Long-term Follow-up of Galactosaemia von Komrower, G. M., Lee, D. H.

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CŒLIAC DISEASE IN A DIABETIC CHILD von Komrower, GeorgeM

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Management of congenital adrenal hyperplasia. Urinary steroid estimations--review of their value von Bailey, C C, Komrower, G M, Palmer, M

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Screening for Phenylketonuria von Komrower, G. M.

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Blood Sugar Levels in Babies Born of Diabetic Mothers von Komrower, George M.

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Management of maternal phenylketonuria: an emerging clinical problem von Komrower, G M, Sardharwalla, I B, Coutts, J M, Ingham, D

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Handicapped children and the attendance allowance von Komrower, G M, Harvey, D R

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Plasma amino acid disturbance in infancy. I: Hypermethioninaemia and transient tyrosinaemia von Komrower, G. M., Robins, A. J.

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Clouds over galactosemia von Komrower, G M

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A Study of the Genetics of Galactosaemia von Holzel, A., Komrower, G. M.

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The Manchester regional screening programme: a 10-year exercise in patient and family care von Komrower, G M, Sardharwalla, I B, Fowler, B, Bridge, C

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Some disturbances of erythrocyte metabolism in galactosaemia von SCHWARZ, V, GOLBERG, L, KOMROWER, G M, HOLZEL, A

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Dietary treatment of homocystinuria von Komrower, G. M., Lambert, A. M., Cusworth, D. C., Westall, R. G.

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Homocystinuria von Komrower, G M, Wilson, V K

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