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van Leusden, MR
Pas, HH
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Citation: Mr. Van Leusden et al., Truncated type XVII collagen expression in a patient with non-Herlitz junctional epidermolysis bullosa caused by a homozygous splice-site mutation, LAB INV, 81(6), 2001, pp. 887-894
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Stouthamer, A
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Jonkman, MF
Citation: A. Stouthamer et al., Normal expression of the 19-DEJ-1 epitope in two siblings with late-onset junctional epidermolysis bullosa, BR J DERM, 144(5), 2001, pp. 1054-1057
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Citation: Rif. Van Der Waal et al., Paraneoplastic pemphigus caused by an epithelioid leiomyosarcoma and associated with fatal respiratory failure, ORAL ONCOL, 36(4), 2000, pp. 390-393
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Molnar, K
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Citation: K. Molnar et al., Two type XVII collagen (BP180) mRNA transcripts in human keratinocytes: a long and a short form, CLIN EXP D, 25(1), 2000, pp. 71-76
Authors:
Fine, JD
Eady, RAJ
Bauer, EA
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Citation: Jd. Fine et al., Revised classification system for inherited epidermolysis bullosa: Report of the Second International Consensus Meeting on diagnosis and classification of epidermolysis bullosa, J AM ACAD D, 42(6), 2000, pp. 1051-1066
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Jonkman, MF
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Citation: D. Zillikens et al., Autoantibodies in anti-p200 pemphigoid stain skin lacking laminin 5 and type VII collagen, BR J DERM, 143(5), 2000, pp. 1043-1049
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Jonkman, MF
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van der Meer, JB
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Pas, HH
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Moog, U
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Scheffer, H
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Jonkman, MF
Citation: U. Moog et al., Epidermolysis bullosa simplex with mottled pigmentation: Clinical aspects and confirmation of the P24L mutation in the KRT5 gene in further patients, AM J MED G, 86(4), 1999, pp. 376-379
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Jonkman, MF
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Citation: Mf. Jonkman et al., Dominant dystrophic epidermolysis bullosa (Pasini) caused by a novel glycine substitution mutation in the type VII collagen gene (COL7A1), J INVES DER, 112(5), 1999, pp. 815-817
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van der Waal, RIF
Pas, HH
Anhalt, GJ
Schulten, EAJM
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Citation: Rif. Van Der Waal et al., Paraneoplastic pemphigus as the presenting symptom of a lymphoma of the tongue, ORAL ONCOL, 34(6), 1998, pp. 567-570
Authors:
Rouan, F
Pulkkinen, L
Jonkman, MF
Bauer, JW
Cserhalmi-Friedman, PB
Christiano, AM
Uitto, J
Citation: F. Rouan et al., Novel and de novo glycine substitution mutations in the type VII collagen gene (COL7A1) in dystrophic epidermolysis bullosa: Implications for geneticcounseling, J INVES DER, 111(6), 1998, pp. 1210-1213