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Citation: M. Paulsen et al., SYNTENIC ORGANIZATION OF THE MOUSE DISTAL CHROMOSOME-7 IMPRINTING CLUSTER AND THE BECKWITH-WIEDEMANN-SYNDROME REGION IN CHROMOSOME 11P15.5, Human molecular genetics (Print), 7(7), 1998, pp. 1149-1159
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Citation: Sc. Clifford et al., MUTATION ANALYSIS OF VON-HIPPEL-LINDAU (VHL) TUMOR SUPPRESSOR-ASSOCIATED PROTEINS, CUL-2 AND VBP-1, IN RENAL-CELL CARCINOMA (RCC), British Journal of Cancer, 78, 1998, pp. 36-36
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DIJKHUIZEN T
DRAAIJERS TG
HULSBEEK MMF
MAHER ER
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Citation: A. Vandenberg et al., ANALYSIS OF MULTIPLE RENAL-CELL ADENOMAS AND CARCINOMAS SUGGESTS ALLELIC LOSS AT 3P21 TO BE A PREREQUISITE FOR MALIGNANT DEVELOPMENT, Genes, chromosomes & cancer, 19(4), 1997, pp. 228-232
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Citation: Ja. Joyce et al., IMPRINTING OF IGF2 AND H19 - LACK OF RECIPROCITY IN SPORADIC BECKWITH-WIEDEMANN-SYNDROME, Human molecular genetics, 6(9), 1997, pp. 1543-1548
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Citation: Er. Woodward et al., GENETIC PREDISPOSITION TO PHEOCHROMOCYTOMA - ANALYSIS OF CANDIDATE GENES GDNF, RET AND VHL, Human molecular genetics, 6(7), 1997, pp. 1051-1056
Citation: Js. Patel et al., FOCAL DERMAL HYPOPLASIA (GOLTZ-SYNDROME) PRESENTING AS A SEVERE FETALMALFORMATION SYNDROME, Clinical dysmorphology, 6(3), 1997, pp. 267-272
Citation: Er. Maher et Ea. Mcniel, PHEOCHROMOCYTOMIA IN DOGS AND CATS, The Veterinary clinics of North America. Small animal practice, 27(2), 1997, pp. 359
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MAHER ER
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Citation: Ar. Webster et al., OCULAR ANGIOMA OCCURRING IN THE ABSENCE OF VON-HIPPEL-LINDAU SYNDROME, Investigative ophthalmology & visual science, 38(4), 1997, pp. 5243-5243
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MCMAHON R
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Citation: Ga. Gregory et al., CYSTIC-FIBROSIS DIAGNOSED BY MOLECULAR-GENETIC INVESTIGATION IN THE MOTHER OF A PATIENT WITH CYSTIC-FIBROSIS, Thorax, 52(1), 1997, pp. 96-97
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LAM WWK
VALLER D
TEMPLE IK
JOYCE JA
REIK W
SCHOFIELD PN
MAHER ER
Citation: D. Catchpoole et al., EPIGENETIC MODIFICATION AND UNIPARENTAL INHERITANCE OF H19 IN BECKWITH-WIEDEMANN-SYNDROME, Journal of Medical Genetics, 34(5), 1997, pp. 353-359