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Henry Madlon
Henry Madlon
Boston Children's Hospital
Congenital nephrotic syndrome
Endocrinology
Nephrosis
Internal medicine
Microcoria
2
Papers
539
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Human laminin β2 deficiency causes congenital nephrosis with mesangial sclerosis and distinct eye abnormalities
2004
Human Molecular Genetics
Martin Zenker
Thomas Aigner
Olaf Wendler
Tim Tralau
Horst Müntefering
Regina Fenski
Susanne Pitz
Valérie Schumacher
Brigitte Royer-Pokora
Elke Wühl
Pierre Cochat
Raymonde Bouvier
Cornelia Kraus
Karlheinz Mark
Henry Madlon
Jörg Dötsch
Wolfgang Rascher
Iwona Maruniak-Chudek
Thomas Lennert
Luitgard M. Neumann
André Reis
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Citations (424)
Congenital nephrosis, mesangial sclerosis, and distinct eye abnormalities with microcoria: an autosomal recessive syndrome.
2004
American Journal of Medical Genetics Part A
Martin Zenker
Tim Tralau
Thomas Lennert
Susanne Pitz
Karlheinz Mark
Henry Madlon
Jörg J. Dötsch
André Reis
Horst Müntefering
Luitgard M. Neumann
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Citations (115)
1