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Installieren Sie die LibKey Nomad-Browsererweiterung und erhalten Sie von vielen Webseiten einfachen Zugriff auf lizenzierte Volltexte oder Open Access Publikationen. Mehr erfahren...Frontiers in genetics, 2024-06, Vol.15, p.1401705
- Peter, Michelle
- Mellis, Rhiannon
- McInnes-Dean, Hannah
- Daniel, Morgan
- Walton, Holly
- Fisher, Jane
- Leeson-Beevers, Kerry
- Allen, Stephanie
- Baple, Emma L
- Beleza-Meireles, Ana
- Bertoli, Marta
- Campbell, Jennifer
- Canham, Natalie
- Cilliers, Deirdre
- Cobben, Jan
- Eason, Jacqueline
- Harrison, Victoria
- Holder-Espinasse, Muriel
- Male, Alison
- Mansour, Sahar
- McEwan, Alec
- Park, Soo-Mi
- Smith, Audrey
- Stewart, Alison
- Tapon, Dagmar
- Vasudevan, Pradeep
- Williams, Denise
- Wu, Wing Han
- Chitty, Lyn S
- Hill, Melissa
2024
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American journal of human genetics, 2001-09, Vol.69 (3), p.493-503
2001
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NIHR open research, 2022, Vol.2, p.10
- Hill, Melissa
- Ellard, Sian
- Fisher, Jane
- Fulop, Naomi
- Knight, Marian
- Kroese, Mark
- Ledger, Jean
- Leeson-Beevers, Kerry
- McEwan, Alec
- McMullan, Dominic
- Mellis, Rhiannon
- Morris, Stephen
- Parker, Michael
- Tapon, Dagmar
- Baple, Emma
- Blackburn, Laura
- Choudry, Asya
- Lafarge, Caroline
- McInnes-Dean, Hannah
- Peter, Michelle
- Ramakrishnan, Rema
- Roberts, Lauren
- Searle, Beverly
- Smith, Emma
- Walton, Holly
- Wynn, Sarah L
- Han Wu, Wing
- Chitty, Lyn S
2022
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Genetics in medicine, 2018-11, Vol.20 (11), p.1430-1437
2018
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The Lancet (British edition), 2019-02, Vol.393 (10173), p.747-757
- Lord, Jenny
- McMullan, Dominic J
- Eberhardt, Ruth Y
- Rinck, Gabriele
- Hamilton, Susan J
- Quinlan-Jones, Elizabeth
- Prigmore, Elena
- Carey, Georgina K
- Mellis, Rhiannon
- Robart, Sarah
- Berry, Ian R
- Chandler, Kate E
- Cilliers, Deirdre
- Cresswell, Lara
- Edwards, Sandra L
- Gardiner, Carol
- Henderson, Alex
- Holden, Simon T
- Homfray, Tessa
- Lester, Tracy
- Newbury-Ecob, Ruth
- Prescott, Katrina
- Quarrell, Oliver W
- Ramsden, Simon C
- Roberts, Eileen
- Tapon, Dagmar
- Tooley, Madeleine J
- Vasudevan, Pradeep C
- Weber, Astrid P
- Wellesley, Diana G
- Westwood, Paul
- White, Helen
- Parker, Michael
- Williams, Denise
- Jenkins, Lucy
- Scott, Richard H
- Kilby, Mark D
- Chitty, Lyn S
- Hurles, Matthew E
- Maher, Eamonn R
- Bateman, Mark
- Best, Sunayna K
- Campbell, Carolyn
- Carey, Georgina
- Cohen, Kelly
- Collingwood, Emma
- Constantinou, Panayiotis
- Delmege, Catherine
- Ellis, Richard
- Evans, Jerry
- Everett, Thomas
- Pinto, Clare F
- Forrester, Natalie
- Fowler, Emma
- Hamilton, Susan
- Healey, Karen
- Hudson, Rebecca
- Keelagher, Rebecca
- Lester, Tracey
- Lewis, Rebecca
- Marton, Tamas
- Mehta, Sarju
- Park, Soo-Mi
- Rowland, Jayne
- Steer, James
- Taylor, Emma J
- Wilson, Elizabeth
2019
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Journal of genetic counseling, 2010-04, Vol.19 (2), p.112-130
2010
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Implementing a rapid fetal exome sequencing service: What do parents and health professionals think?
2022
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European journal of human genetics : EJHG, 2024-10
2024
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Prenatal diagnosis, 2022-01, Vol.42 (1), p.97-108
2022
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Prenatal diagnosis, 2024-04, Vol.44 (4), p.465-479
- McInnes-Dean, Hannah
- Mellis, Rhiannon
- Daniel, Morgan
- Walton, Holly
- Baple, Emma L
- Bertoli, Marta
- Fisher, Jane
- Gajewska-Knapik, Katarzyna
- Holder-Espinasse, Muriel
- Lafarge, Caroline
- Leeson-Beevers, Kerry
- McEwan, Alec
- Pandya, Pranav
- Parker, Michael
- Peet, Sophie
- Roberts, Lauren
- Sankaran, Srividhya
- Smith, Audrey
- Tapon, Dagmar
- Wu, Wing Han
- Wynn, Sarah L
- Chitty, Lyn S
- Hill, Melissa
- Peter, Michelle
2024
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Obstetrical & gynecological survey, 2019-04, Vol.74 (4), p.202-204
2019
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Prenatal diagnosis, 2016-08, Vol.36 (8), p.708-713
2016
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Prenatal diagnosis, 2016-08, Vol.36 (8), p.708-713
2016
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Journal of genetic counseling, 1999-08, Vol.8 (4), p.235-246
1999
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Obstetrical & gynecological survey, 2019-07, Vol.74 (7), p.394-396
- Lord, Jenny
- McMullan, Dominic J.
- Eberhardt, Ruth Y.
- Rinck, Gabriele
- Hamilton, Susan J.
- Quinlan-Jones, Elizabeth
- Prigmore, Elena
- Keelagher, Rebecca
- Best, Sunayna K.
- Carey, Georgina K.
- Mellis, Rhiannon
- Robart, Sarah
- Berry, Ian R.
- Chandler, Kate E.
- Cilliers, Deirdre
- Cresswell, Lara
- Edwards, Sandra L.
- Gardiner, Carol
- Henderson, Alex
- Holden, Simon T.
- Homfray, Tessa
- Lester, Tracy
- Lewis, Rebecca A.
- Newbury-Ecob, Ruth
- Prescott, Katrina
- Quarrell, Oliver W.
- Ramsden, Simon C.
- Roberts, Eileen
- Tapon, Dagmar
- Tooley, Madeleine J.
- Vasudevan, Pradeep C.
- Weber, Astrid P.
- Wellesley, Diana G.
- Westwood, Paul
- White, Helen
- Parker, Michael
- Williams, Denise
- Jenkins, Lucy
- Scott, Richard H.
- Kilby, Mark D.
- Chitty, Lyn S.
- Hurles, Matthew E.
- Maher, Eamonn R.
2019
Volltextzugriff (PDF)
NIHR open research, 2022-01, Vol.2, p.10-10
- Hill, Melissa
- Ellard, Sian
- Fisher, Jane
- Fulop, Naomi
- Knight, Marian
- Kroese, Mark
- Ledger, Jean
- Leeson-Beevers, Kerry
- McEwan, Alec
- McMullan, Dominic
- Mellis, Rhiannon
- Morris, Stephen
- Parker, Michael
- Tapon, Dagmar
- Baple, Emma
- Blackburn, Laura
- Choudry, Asya
- Lafarge, Caroline
- McInnes-Dean, Hannah
- Peter, Michelle
- Ramakrishnan, Rema
- Roberts, Lauren
- Searle, Beverly
- Smith, Emma
- Walton, Holly
- Wynn, Sarah L.
- Han Wu, Wing
- Chitty, Lyn S.
2022
Volltextzugriff (PDF)
American journal of medical genetics. Part A, 2011-10, Vol.155A (10), p.2397-2408
- Holman, Sarah K.
- Daniel, Phil
- Jenkins, Zandra A.
- Herron, Rachel L.
- Morgan, Tim
- Savarirayan, Ravi
- Chow, C.W.
- Bohring, Axel
- Mosel, Annette
- Lacombe, Didier
- Steiner, Bernhard
- Schmitt-Mechelke, Thomas
- Schroter, Barbara
- Raas-Rothschild, Annick
- Miñaur, Sixto Garcia
- Porteous, Mary
- Parker, Michael
- Quarrell, Oliver
- Tapon, Dagmar
- Cormier-Daire, Valérie
- Mansour, Sahar
- Nash, Ruth
- Bindoff, Laurence A.
- Fiskerstrand, Torunn
- Robertson, Stephen P.
2011
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