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| 1 | Molecular genetic analysis of FIH-1, FH, and SDHB candidate tumour suppressor genes in renal cell carcinoma显示文摘 | Morris MR Maina E Morgan NV | 2004 | J Clin Pathol2004，57，7： | 1 |
| 2 | PLAgG6, encoding a phospholipase A2, is mutated in neurodegenerative disorders with high brain iron显示文摘 | Morgan NV Westaway SK Morton JE | 2006 | Nat Genet2006，38，7： | 1 |
| 3 | Mutations in SLC29A3,encoding an equilibrative nucleoside transporter ENT3,cause a familial histiocytosis syndrome (Faisalabad histiocytosis) and familial Rosai-Dorfman disease显示文摘 | Morgan NV Morris MR | | 0，，02： | 1 |
| 4 | A germline mutation in BLOC1S3/reduced pigmentation causes a novel variant of Hermansky-Pudlak syndrome (HPS8)显示文摘 | Morgan NV Pasha S Johnson CA | 2006 | Am J Hum Genet2006，78，1： | 1 |
| 5 | A locus for asphyxiating thoracic dystrophy,ATD,maps to chromosome 15q13 显示文摘 | Morgan NV Bacchelli C Gissen P | 2003 | J Med Genet2003，40，6： | 1 |
| 6 | A locus for asphyxiating thorac- ic dystrophy,ATD,maps to chromosome 15q13显示文摘 | Morgan NV Bacchelli C Gissen P | 2003 | J Med Genet2003，40，： | 1 |
| 7 | Mutations io VPS33B,encoding a regulator of SNARE-dependent membrane fusion,cause arthrogryposis-renal dysfunction-cholestasis (ARC)syndrome显示文摘 | Gissen P Johnson CA Morgan NV | | 0，，： | 1 |
| 8 | PLA2G6, encoding a phospholipase A2, is mutated in neurodegenerative disorders with high brain iron显示文摘 | Morgan NV Westaway SK Morton JE | 2006 | Nat Genet2006，38，7： | 1 |
| 9 | A novel locus for Meckel - Gruber syndrome, MKS3, maps to chromosome 8q24显示文摘 | Morgan NV Gissen P Sharif SM | 2002 | Hum Genet2002，111，45： | 1 |
| 10 | A common Faneoni anemia mutation in black populations of sub-Saharan Africa显示文摘 | Morgan NV Essop F Demuth I | 2005 | Blood2005，105，9： | 1 |
| 11 | Mutation in the TCRα subunit constant gene (TRAC) leads to a human immunodeficiency disorder characterized by a lack of TCRαβ + T cells显示文摘 | Morgan NV Goddard S Cardno TS | | 0，，02： | 1 |
| 12 | PLA2C-6, encoding a phospholipase A2, is mutated in neurodegenerative disorders with high brain iron显示文摘 | Morgan NV Westaway SK Morton JE | 2006 | Nat Genet2006，38，7： | 1 |
| 13 | A Incus for asphyxiating thoracic dys- trophy,ATD, maps to chromosome 15q13 显示文摘 | Morgan NV Bacchelli C Gissen P | 2003 | J Med C enet2003，40，6： | 1 |
| 14 | Mutations in VPS33 B,encoding a regulator of SNARE-dependent membrane fusion,cause arthrogryposis-renal dysfunction-cholestasis (ARC) syndrome显示文摘 | Gissen P Johnson CA Morgan NV | | 0，，04： | 1 |
| 15 | A locus for asphyxiating thoracic dystrophy,ATD,maps to chromosome 15q13显示文摘 | Morgan NV Bacchelli C Gissen P | 2003 | Med J G enet2003，40，6： | 1 |
| 16 | PLA2G6, encoding a phospholipase A2, is mutated in neurodegenerative disorders with high brain iron显示文摘 | Morgan NV Westaway SK Morton JEV | 2006 | Nature Genet2006，38，： | 1 |
| 17 | Molecular genetic analysis of FIH-1,FH,and SDHB candidate tumour suppressor genes in renal cell carcinoma显示文摘 | Morris MR Maina E Morgan NV | 2004 | J Clin Pathol2004，57，7： | 1 |
| 18 | A germline mutation in BLOC1S3/reduced pigmentation causes a novel variant of Hermansky-Pudlak syndrome (HPS8)显示文摘 | Morgan NV Pasha S Johnson CA | 2006 | Am J Hum Genet2006，78，： | 1 |
| 19 | A locus for asphyxiating thoracic dystrophy,ATD,maps to chromosome 15q13显示文摘 | Morgan NV Bacchelli C Gissen P | | 0，，： | 1 |
| 20 | A locus for asphyxiating thoracic dystrophy, ATD, maps to chromosome 15 q13 显示文摘 | Morgan NV Bacchelli C Gissen P | 2003 | J Med Genet2003，40，6： | 1 |
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