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Hans-Gerd Kehl
Hans-Gerd Kehl
Boston Children's Hospital
Singleton Merten syndrome
Calcification
Dominance (genetics)
Biology
Missense mutation
4
Papers
197
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Singleton-Merten Syndrome: a rare autoimmune disorder caused by a specific IFIH1 mutation.
2015
Molecular and Cellular Pediatrics
Insa Buers
Yvonne Nitschke
Raoul C. M. Hennekam
Mary MacDougall
Changming Lu
Olga A. Mamaeva
Gillian I. Rice
Heidi Erlandsen
Hans-Gerd Kehl
Holger Thiele
Peter Nürnberg
Wolfgang Höhne
Yanick J. Crow
A Feigenbaum
Frank Rutsch
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A Specific IFIH1 Gain-of-Function Mutation Causes Singleton-Merten Syndrome
2015
American Journal of Human Genetics
Frank Rutsch
Mary MacDougall
Changming Lu
Insa Buers
Olga A. Mamaeva
Yvonne Nitschke
Gillian I. Rice
Heidi Erlandsen
Hans-Gerd Kehl
Holger Thiele
Peter Nürnberg
Wolfgang Höhne
Yanick J. Crow
Annette Feigenbaum
Raoul C. M. Hennekam
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Citations (138)
Singleton–Merten syndrome: An autosomal dominant disorder with variable expression
2013
American Journal of Medical Genetics Part A
Annette Feigenbaum
Christine Muller
Christopher Yale
Johannes Kleinheinz
Peter A. Jezewski
Hans-Gerd Kehl
Mary MacDougall
Frank Rutsch
Raoul C. M. Hennekam
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Citations (46)
Do the Age of Patients with Tetralogy of Fallot at the Time of Surgery and the Applied Surgical Technique Influence the Reoperation Rate
2009
Herz
Christoph Gerling
Andreas Rukosujew
Hans-Gerd Kehl
Tonny D.T. Tjan
A. Hoffmeier
Johannes Vogt
H.H Scheld
Thomas Krasemann
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Citations (13)
1