Alport's syndrome von Crawfurd, M A

Volltext

Review: Genetics of steroid sulphatase deficiency and X‐linked ichthyosis von Crawfurd, M. A.

Volltext

Anderson-Fabry disease von Morgan, S. H., Crawfurd, M. A.

Volltext

Dermatoglyphics in partial C trisomies von Crawfurd, M A

Volltext

Recognising Placental Steroid Sulphatase Deficiency von Harkness, R. A., Taylor, N. F., Crawfurd, M. A., Rose, F. A.

Volltext

A further family with congenital renal proximal tubular dysgenesis von MacMahon, P, Blackie, R A, House, M J, Risdon, R A, Crawfurd, M D

Volltext

Congenital haemolytic anaemia resulting from glucose phosphate isomerase deficiency: genetics, clinical picture, and prenatal diagnosis von Whitelaw, A G, Rogers, P A, Hopkinson, D A, Gordon, H, Emerson, P M, Darley, J H, Reid, C, Crawfurd, M A

Volltext

Early Prenatal Diagnosis of Hurler's Syndrome with Termination of Pregnancy and Confirmatory Findings on the Fetus von Crawfurd, M. d'A., Dean, M. F., Hunt, D. M., Johnson, D. R., MacDonald, R. R., Muir, H., Wright, E. A. Payling, Wright, C. R. Payling

Volltext

Investigation of three patients with the ring syndrome, including familial transmission of ring 5, and estimation of reproductive risks von MACDERMOT, K. D, JACK, E, COOKE, A, TURLEAU, C, LINDENBAUM, R. H, PEARSON, J, PATEL, C, BARNES, P. M, PORTCH, J, CRAWFURD, M. A

Volltext

Paterson-Kelly Syndrome in Adolescence von Crawfurd, M. D'A., Jacobs, A., Murphy, B., Peters, D. K.

Volltext

Family Stigma In Congenital Physical Handicap von Crawfurd, M. d'A

Volltext

Paterson–Kelly Syndrome in Adolescence: A Report of Five Cases von Crawfurd, M. D'A., Jacobs, A., Murphy, B., Peters, D. K.

Volltext

Interstitial deletions without phenotypic effect : prenatal diagnisis of a new family and brief review von BARBER, J. C. K, MAHL, H, PORTCH, J, CRAWFURD, M. A

Volltext

Elements of Medical Genetics von Crawfurd, M. D'A.

Volltext

Studies on human phenylalanine mono‐oxygenase. I. Restricted expression von Crawfurd, M. A., Gibbs, D. A., Sheppard, D. M.

Volltext

Anderson-Fabry disease--family linkage studies using two polymorphic X-linked DNA probes von Morgan, S H, Cheshire, J K, Wilson, T M, MacDermot, K, Crawfurd, M A

Volltext

The demonstration of monozygosity in twins discordant for sacral agenesis von Crawfurd, M D, Cheshire, J, Wilson, T M, Woodhouse, C R

Volltext

Any Questions von Crawfurd, M. d'A.

Volltext

Screening for Phenylketonuria von Andrews, T. M., McKeran, R. O.

Volltext

Genetic counseling: 3rd edn. W. Fuhrmann and F. Vogel. Translated from the German by S. Kurth‐Scherer. Springer‐Verlag, Berlin‐Heidelberg‐New York, 1983, 180 pp., DM 42 von Crawfurd, M. d'A.

Volltext