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Results: 1-7 |
Results: 7
THE IMPACT OF MOLECULAR DIAGNOSIS ON FAMILIAL COLORECTAL-CANCER
Authors: BENNETT G RUDZKI Z COLE S YOUNG G SUTHERS G
Citation: G. Bennett et al., THE IMPACT OF MOLECULAR DIAGNOSIS ON FAMILIAL COLORECTAL-CANCER, CLINICAL CHEMISTRY AND LABORATORY MEDICINE, 36(8), 1998, pp. 641-644
FAMILIAL NEURONAL INTRANUCLEAR INCLUSION DISEASE WITH UBIQUITIN POSITIVE INCLUSIONS
Authors: KIMBER TE BLUMBERGS PC RICE JP HALLPIKE JF EDIS R THOMPSON PD SUTHERS G
Citation: Te. Kimber et al., FAMILIAL NEURONAL INTRANUCLEAR INCLUSION DISEASE WITH UBIQUITIN POSITIVE INCLUSIONS, Journal of the neurological sciences, 160(1), 1998, pp. 33-40
FRONTO-FACIO-NASAL DYSPLASIA
Authors: SUTHERS G DAVID D CLARK B
Citation: G. Suthers et al., FRONTO-FACIO-NASAL DYSPLASIA, Clinical dysmorphology, 6(3), 1997, pp. 245-249
LIVE UNIVERSES
Authors: SUTHERS G
Citation: G. Suthers, LIVE UNIVERSES, Nature, 385(6612), 1997, pp. 109-109
MOST GERM-LINE MUTATIONS IN THE NEVOID BASAL-CELL CARCINOMA SYNDROME LEAD TO A PREMATURE TERMINATION OF THE PATCHED PROTEIN, AND NO GENOTYPE-PHENOTYPE CORRELATIONS ARE EVIDENT
Authors: WICKING C SHANLEY S SMYTH I GILLIES S NEGUS K GRAHAM S SUTHERS G HAITES N EDWARDS M WAINWRIGHT B CHENEVIXTRENCH G
Citation: C. Wicking et al., MOST GERM-LINE MUTATIONS IN THE NEVOID BASAL-CELL CARCINOMA SYNDROME LEAD TO A PREMATURE TERMINATION OF THE PATCHED PROTEIN, AND NO GENOTYPE-PHENOTYPE CORRELATIONS ARE EVIDENT, American journal of human genetics, 60(1), 1997, pp. 21-26
MUTATIONS, MALFORMATIONS AND MORTALITY
Authors: SUTHERS G
Citation: G. Suthers, MUTATIONS, MALFORMATIONS AND MORTALITY, Journal of paediatrics and child health, 32(1), 1996, pp. 10-15
SPORADIC MOTONEURON DISEASE DUE TO FAMILIAL SOD1 MUTATION WITH LOW PENETRANCE
Authors: SUTHERS G LAING N WILTON S DOROSZ S WADDY H
Citation: G. Suthers et al., SPORADIC MOTONEURON DISEASE DUE TO FAMILIAL SOD1 MUTATION WITH LOW PENETRANCE, Lancet, 344(8939-4), 1994, pp. 1773-1773
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