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Results: 1-6 |
Results: 6

Authors: PHILLIPS MF ROGERS MT BARNETSON R BRAUN C HARLEY HG MYRING J STEVENS D WILES CM HARPER PS
Citation: Mf. Phillips et al., PROMM - THE EXPANDING PHENOTYPE - A FAMILY WITH PROXIMAL MYOPATHY, MYOTONIA AND DEAFNESS, Neuromuscular disorders, 8(7), 1998, pp. 439-446

Authors: LANCASTER JM CARNEY ME GRAY J MYRING J GUMBS C SAMPSON J WHEELER D FRANCE E WISEMAN R HARPER P FUTREAL PA
Citation: Jm. Lancaster et al., BRCA1 AND BRCA2 IN BREAST-CANCER FAMILIES FROM WALES - MODERATE MUTATION FREQUENCY AND 2 RECURRENT MUTATIONS IN BRCA1, British Journal of Cancer, 78(11), 1998, pp. 1417-1420

Authors: MAHESHWAR MM CHEADLE JP JONES AC MYRING J FRYER AE HARRIS PC SAMPSON JR
Citation: Mm. Maheshwar et al., THE GAP-RELATED DOMAIN OF TUBERIN, THE PRODUCT OF THE TSC2 GENE, IS ATARGET FOR MISSENSE MUTATIONS IN TUBEROUS SCLEROSIS, Human molecular genetics, 6(11), 1997, pp. 1991-1996

Authors: REARDON W MACMILLAN JC MYRING J HARLEY HG RUNDLE SA BECK L HARPER PS SHAW DJ
Citation: W. Reardon et al., CATARACT AND MYOTONIC-DYSTROPHY - THE ROLE OF MOLECULAR DIAGNOSIS, British journal of ophthalmology, 77(9), 1993, pp. 579-583

Authors: HARPER PS MYRING J PHILLIPS M HARLEY H MEREDITH AL MACMILLAN J SHAW DJ
Citation: Ps. Harper et al., MOLECULAR-GENETIC TESTING FOR MYOTONIC-DYSTROPHY - PRACTICAL AND ETHICAL CONSIDERATION, American journal of human genetics, 53(3), 1993, pp. 1820-1820

Authors: HARLEY HG RUNDLE SA MACMILLAN JC MYRING J BROOK JD CROW S REARDON W FENTON I SHAW DJ HARPER PS
Citation: Hg. Harley et al., SIZE OF THE UNSTABLE CTG REPEAT SEQUENCE IN RELATION TO PHENOTYPE ANDPARENTAL TRANSMISSION IN MYOTONIC-DYSTROPHY, American journal of human genetics, 52(6), 1993, pp. 1164-1174
Risultati: 1-6 |