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Alport's syndromeCRAWFURD, M. A.Journal of medical genetics. 1988, Vol 25, Num 9, pp 623-627, issn 0022-2593Article

SYNDROMES OF MICROCEPHALY, MICROPHTHALMIA CATARACTS, AND JOINT CONTRACTURESWINTER RM; DONNAI D; D'A CRAWFURD M et al.1981; J. MED. GENET.; ISSN 0022-2593; GBR; DA. 1981; VOL. 18; NO 2; PP. 129-133; BIBL. 16 REF.Article

NON-PROGRESSIVE CEREBELLAR ATASIA, APLASIA OF PUPILLARY ZONE OF IRIS, AND MENTAL SUBNORMALITY (GILLESPIE'S SYNDROME) AFFECTING 3 MEMBERS OF A NON-CONSANGUINEOUS FAMILY IN 2 GENERATIONSCRAWFURD M D'A; HARCOURT RB; SHAW PA et al.1979; J. MED. GENET.; GBR; DA. 1979; VOL. 16; NO 5; PP. 373-378; BIBL. 13 REF.Article

Ethical guidelines in fetal medicineCRAWFURD, M. D.Fetal therapy. 1987, Vol 2, Num 3, pp 175-180, issn 0257-2788Article

STUDIES ON HUMAN PHENYLALANINE MONO-OXYGENASE. I: RESTRICTED EXPRESSIONCRAWFURD M D'A; GIBBS DA; SHEPPARD DM et al.1981; J. INHERIT. METAB. DIS.; ISSN 0141-8955; GBR; DA. 1981; VOL. 4; NO 4; PP. 191-195; BIBL. 24 REF.Article

CONGENITAL HAEMOLYTIC ANAEMIA RESULTING FROM GLUCOSE PHOSPHATE ISOMERASE DEFICIENCY: GENETICS, CLINICAL PICTURE AND PRENATAL DIAGNOSISWHITELAW AGL; ROGERS PA; HOPKINSON DA et al.1979; J. MED. GENET.; GBR; DA. 1979; VOL. 16; NO 3; PP. 189-196; BIBL. 32 REF.Article

Interstitial deletions without phenotypic effect : prenatal diagnisis of a new family and brief reviewBARBER, J. C. K; MAHL, H; PORTCH, J et al.Prenatal diagnosis. 1991, Vol 11, Num 6, pp 411-416, issn 0197-3851, 6 p.Article

A further family with congenital renal proximal tubular dysgenesisMACMAHON, P; BLACKIE, R. A. S; HOUSE, M. J et al.Journal of medical genetics. 1990, Vol 27, Num 6, pp 395-398, issn 0022-2593Article

First-trimester diagnosis of Lesch-Nyhan syndromeGIBBS, D. A; MCFADYEN, I. R; CRAWFURD, M. D'A et al.Lancet (British edition). 1984, Vol 2, Num 8413, pp 1180-1183, issn 0140-6736Article

Investigation of three patients with the ring syndrome, including familial transmission of ring 5, and estimation of reproductive risksMACDERMOT, K. D; JACK, E; COOKE, A et al.Human genetics. 1990, Vol 85, Num 5, pp 516-520, issn 0340-6717, 5 p.Article

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