Showing 1–12 of 12 results
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Amendments and Corrections |
Erratum: Mutations in different components of FGF signaling in LADD syndrome
- Edyta Rohmann
- , Han G Brunner
- , Hülya Kayserili
- , Oya Uyguner
- , Gudrun Nürnberg
- , Erin D Lew
- , Angus Dobbie
- , Veraragavan P Eswarakumar
- , Abdullah Uzumcu
- , Melike Ulubil-Emeroglu
- , Jules G Leroy
- , Yun Li
- , Christian Becker
- , Kai Lehnerdt
- , Cor W R J Cremers
- , Memnune Yüksel-Apak
- , Peter Nürnberg
- , Christian Kubisch
- , Joseph Schlessinger
- , Hans van Bokhoven
- & Bernd Wollnik
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Amendments and Corrections |
Erratum to: Stickler syndrome caused by COL2A1 mutations: genotype–phenotype correlation in a series of 100 patients
- Kristien P Hoornaert
- , Inge Vereecke
- , Chantal Dewinter
- , Thomas Rosenberg
- , Frits A Beemer
- , Jules G Leroy
- , Laila Bendix
- , Erik Björck
- , Maryse Bonduelle
- , Odile Boute
- , Valerie Cormier-Daire
- , Christine De Die-Smulders
- , Anne Dieux-Coeslier
- , Hélène Dollfus
- , Mariet Elting
- , Andrew Green
- , Veronica I Guerci
- , Raoul CM Hennekam
- , Yvonne Hilhorts-Hofstee
- , Muriel Holder
- , Carel Hoyng
- , Kristi J Jones
- , Dragana Josifova
- , Ilkka Kaitila
- , Suzanne Kjaergaard
- , Yolande H Kroes
- , Kristina Lagerstedt
- , Melissa Lees
- , Martine LeMerrer
- , Cinzia Magnani
- , Carlo Marcelis
- , Loreto Martorell
- , Michèle Mathieu
- , Meriel McEntagart
- , Angela Mendicino
- , Jenny Morton
- , Gabrielli Orazio
- , Véronique Paquis
- , Orit Reish
- , Kalle OJ Simola
- , Sarah F Smithson
- , Karen I Temple
- , Elisabeth Van Aken
- , Yolande Van Bever
- , Jenneke van den Ende
- , Johanna M Van Hagen
- , Leopoldo Zelante
- , Riina Zordania
- , Anne De Paepe
- , Bart P Leroy
- , Marc De Buyzere
- , Paul J Coucke
- & Geert R Mortier
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Mutations in different components of FGF signaling in LADD syndrome
- Edyta Rohmann
- , Han G Brunner
- , Hülya Kayserili
- , Oya Uyguner
- , Gudrun Nürnberg
- , Erin D Lew
- , Angus Dobbie
- , Veraragavan P Eswarakumar
- , Abdullah Uzumcu
- , Melike Ulubil-Emeroglu
- , Jules G Leroy
- , Yun Li
- , Christian Becker
- , Kai Lehnerdt
- , Cor W R J Cremers
- , Memnune Yüksel-Apak
- , Peter Nürnberg
- , Christian Kubisch
- , Joseph Schlessinger
- , Hans van Bokhoven
- & Bernd Wollnik
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Research |
Stickler syndrome caused by COL2A1 mutations: genotype–phenotype correlation in a series of 100 patients
- Kristien P Hoornaert
- , Inge Vereecke
- , Chantal Dewinter
- , Thomas Rosenberg
- , Frits A Beemer
- , Jules G Leroy
- , Laila Bendix
- , Erik Björck
- , Maryse Bonduelle
- , Odile Boute
- , Valerie Cormier-Daire
- , Christine De Die-Smulders
- , Anne Dieux-Coeslier
- , Hélène Dollfus
- , Mariet Elting
- , Andrew Green
- , Veronica I Guerci
- , Raoul C M Hennekam
- , Yvonne Hilhorts-Hofstee
- , Muriel Holder
- , Carel Hoyng
- , Kristi J Jones
- , Dragana Josifova
- , Ilkka Kaitila
- , Suzanne Kjaergaard
- , Yolande H Kroes
- , Kristina Lagerstedt
- , Melissa Lees
- , Martine LeMerrer
- , Cinzia Magnani
- , Carlo Marcelis
- , Loreto Martorell
- , Michèle Mathieu
- , Meriel McEntagart
- , Angela Mendicino
- , Jenny Morton
- , Gabrielli Orazio
- , Véronique Paquis
- , Orit Reish
- , Kalle O J Simola
- , Sarah F Smithson
- , Karen I Temple
- , Elisabeth Van Aken
- , Yolande Van Bever
- , Jenneke van den Ende
- , Johanna M Van Hagen
- , Leopoldo Zelante
- , Riina Zordania
- , Anne De Paepe
- , Bart P Leroy
- , Marc De Buyzere
- , Paul J Coucke
- & Geert R Mortier
