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Author/Creator Monk, David

1. A New Overgrowth Syndrome is due to Mutations in RNF125. Issue 12 (December 2014)

Authors:
Tenorio, Jair; Mansilla, Alicia; Valencia, María; Martínez‐Glez, Víctor; Romanelli, Valeria; Arias, Pedro; Castrejón, Nerea; Poletta, Fernando; Guillén‐Navarro, Encarna; Gordo, Gema; Mansilla, Elena; García‐Santiago, Fé; González‐Casado, Isabel; Vallespín, Elena; Palomares, María; Mori, María A.;...
Journal:
Human mutation
Issue:
Volume 35:Issue 12(2014:Dec.)
Page Start:
1436
Record Type:
Journal Article
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2. Barrett's oesophagus patients attending hospital: Baseline clinical, patient history and quality of life data from BOSS and AspECT. Issue 11 (November 2016)

Authors:
Love, Sharon; Reilly, Gavin; Roberts, Corran; Wise, Adelyn; Moayyedi, Paul; Foy, Chris; Stokes, Clive; De Caestecker, John; Attwood, Stephen; Watson, Peter; Ang, Yeng; Bhandiri, Pradeep; Old, Oliver; Hapeshi, Julie; Penman, Ian; Rodgers, Colin; Edwards, Cathryn; Monk, David; Ragunath, Krish; Morr...
Journal:
European journal of surgical oncology
Issue:
Volume 42:Issue 11(2016:Nov.)
Page Start:
S223
Record Type:
Journal Article
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4. Characterization of parent-of-origin methylation using the Illumina Infinium MethylationEPIC array platform. (2nd July 2018)

Authors:
Hernandez Mora, Jose R; Tayama, Chiharu; Sánchez-Delgado, Marta; Monteagudo-Sánchez, Ana; Hata, Kenichiro; Ogata, Tsutomu; Medrano, Jose; Poo-Llanillo, Maria E; Simón, Carlos; Moran, Sebastian; Esteller, Manel; Tenorio, Jair; Lapunzina, Pablo; Kagami, Masayo; Monk, David; Nakabayashi, Kazuhiko
Journal:
Epigenomics
Issue:
Volume 10:Number 7(2018)
Page Start:
941
Record Type:
Journal Article
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5. Clinical and molecular analyses of Beckwith–Wiedemann syndrome: Comparison between spontaneous conception and assisted reproduction techniques. Issue 10 (2nd August 2016)

Authors:
Tenorio, Jair; Romanelli, Valeria; Martin‐Trujillo, Alex; Fernández, García‐Moya; Segovia, Mabel; Perandones, Claudia; Pérez Jurado, Luis A.; Esteller, Manel; Fraga, Mario; Arias, Pedro; Gordo, Gema; Dapía, Irene; Mena, Rocío; Palomares, María; Pérez de Nanclares, Guiomar; Nevado, Julián; García‐...
Other Names:
Hennekam Raoul C.M. guestEditor.; Biesecker Leslie G. guestEditor.
Journal:
American journal of medical genetics
Issue:
Volume 170:Issue 10(2016)
Page Start:
2740
Record Type:
Journal Article
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10. Erratum to: Imprinting disorders: a group of congenital disorders with overlapping patterns of molecular changes affecting imprinted loci. Issue 1 (December 2016)

Authors:
Eggermann, Thomas; de Nanclares, Guiomar; Maher, Eamonn; Temple, I.; Tümer, Zeynep; Monk, David; Mackay, Deborah; Grønskov, Karen; Riccio, Andrea; Linglart, Agnès; Netchine, Irène
Journal:
Clinical epigenetics
Issue:
Volume 8:Issue 1(2016)
Page Start:
1
Record Type:
Journal Article
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