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| 1 | Hypophos-phatasia associated with increased nuchal translucency: a report of two affected pregnancies 显示文摘 | Souka AP Raymond FL Mornet E | 2002 | Ultrasound Obstet Gynecol2002，20，5： | 1 |
| 2 | X linked mental retardation: a clinical guide显示文摘 | Raymond FL | 2006 | J Med Genet2006，43，3： | 1 |
| 3 | Adenovirus-mediated p53 gene therapy for human gliomas显示文摘 | Frederick FL Alfred Y Raymond S | 1999 | Neurosurgery1999，45，4： | 1 |
| 4 | Hypophosphatasia associatedwith increased nuchal translucency:a report of two affected pregnancies显示文摘 | Souka AP Raymond FL Mornet E | | 0，，03： | 1 |
| 5 | Molecular prenatal diagnosis: the impact of modem technologies 显示文摘 | Raymond FL Whittaker J Jenkins L | 2010 | Prenat Diagn2010，30，7： | 1 |
| 6 | X linked mental retardation: a clinical guide 显示文摘 | Raymond FL | 2006 | MedGenet2006，43，3： | 1 |
| 7 | Cloning, genomic organization, alternative splicing and expression analysis of the human gene WNK3 ( PRKWNK3 ) 显示文摘 | Holden S Cox J Raymond FL | 2004 | Gene2004，335，： | 1 |
| 8 | The genetics of mental retardation 显示文摘 | Raymond FL Tarpey P | 2006 | Human Molecular Genetics2006，15，： | 1 |
| 9 | The antigenicity and evolution of influenza H1 haemagglutinin,from 1950-1957 and 1977-1983:two pathways from one gene显示文摘 | Raymond FL Caton AJ Cox NJ | | 0，，02： | 1 |
| 10 | Mutations in CUIAB, which encodes a ubiquitin E3 ligase subunit, cause an X - linked mental retardation syndrome associated with aggressive outbursts, seizures, relative macrocephaly, central obesity, hypogonadism, pes cavus, and tremor 显示文摘 | Tarpey PS Raymond FL O' Meara S | 2007 | Am J Hum C enet2007，80，2： | 1 |
| 11 | The antigenicity and evolution of influenza H1 haem- agglutinin, from 1950-1957 and 1977-1983: Two pathways from one gene 显示文摘 | Raymond FL Caton AJ Cox NJ Kendal AP Brownlee GG | 1986 | Virology1986，148，2： | 1 |
| 12 | Molecular prenatal diagnosis: The impact of modern technologies显示文摘 | Raymond FL Whittaker J Jenkins L | 2010 | Prenat Diagn2010，30，7： | 1 |
| 13 | Mutations in CUL4B, which encodes a ubiquitin E3 ligase subunit, cause an X - linked mental retardation syndrome associated with aggressive outbursts, seizures, relative maerocephaly, central obesity, hypogonadism, pes cavus, and tremor显示文摘 | Tarpey PS Raymond FL O'Meara S | 2007 | Am J Hum Genet2007，80，2： | 1 |
| 14 | Cloning,genomic organization,alternative splicing and expression analysis of the human gene WNK3 (PRKWNK3)显示文摘 | Cox J Raymond FL | 2004 | Gene2004，335，： | 1 |
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