@article{UBHD-69124813,
  author={Anton-Lamprecht, Ingrun},
  title={Besserung einer Ichthyosis congenita nach Varizellen-Infektion},
  year={1996},
  pages={869-870},
  language={ger},
  issn={1432-1173},
  volume={47},
  number={11},
  note={Gesehen am 27.09.2023},
  journal={Der Hautarzt},
  doi={10.1007/s001050050525},
}
@incollection{UBHD-69131767,
  author={Anton-Lamprecht, Ingrun},
  title={Bullous diseases},
  year={1995},
  pages={53-54},
  language={eng},
  isbn={0-444-81917-7 and 978-0-444-81917-8},
  booktitle={Pediatric dermatology},
}
@article{UBHD-69126431,
  author={Anton-Lamprecht, Ingrun},
  title={Epidermolysis bullosa herpetiformis Dowling-Meara},
  year={1994},
  pages={716-719},
  language={ger},
  issn={0301-0481},
  volume={69},
  journal={H + G},
}
@incollection{UBHD-69132586,
  author={Anton-Lamprecht, Ingrun and Gedde-Dahl, Tobias},
  title={Epidermolysis bullosa},
  year={1997},
  language={eng},
  journal={Emery and Rimoin's principles and practice of medical genetics ; Vol. 1},
}
@article{UBHD-69124807,
  author={Anton-Lamprecht, Ingrun},
  title={Keratin clumping in epidermolysis bullosa, Dowling‐Meara type},
  year={1996},
  pages={184-185},
  language={eng},
  issn={1365-2133},
  volume={134},
  number={1},
  note={Gesehen am 27.09.2023},
  journal={British journal of dermatology},
  doi={10.1111/j.1365-2133.1996.tb07868.x},
}
@article{UBHD-69131766,
  author={Anton-Lamprecht, Ingrun and McGarth, John A. and Christiano, Angela M. and Uitto, Jouni},
  title={Mutations in the laminin 5 LAMB3 gene in generalized atrophic benign epidermolysis bullosa},
  year={1995},
  pages={856-857},
  language={eng},
  issn={1523-1747},
  volume={105},
  number={6},
  note={Gesehen am 19.10.2023 ; Elektronische Reproduktion der Druck-Ausgabe 4. Januar 2016},
  journal={The journal of investigative dermatology},
  doi={10.1111/1523-1747.ep12326697},
}
@article{UBHD-69125126,
  author={Anton-Lamprecht, Ingrun and Rauskolb, R{\"u}diger},
  title={Pr{\"a}natale Diagnostik von Genodermatosen},
  year={1994},
  pages={296-308},
  language={ger},
  issn={0017-5994},
  volume={27},
  journal={Der Gyn{\"a}kologe},
}
@incollection{UBHD-69124866,
  author={Anton-Lamprecht, Ingrun},
  title={Prenatal diagnosis of genodermatoses},
  year={1996},
  pages={333-384},
  language={eng},
  isbn={0-8247-9401-X and 978-0-8247-9401-9},
  booktitle={Skin changes and diseases in pregnancy},
  editor={Harahap, Marwali},
}
@incollection{UBHD-69131769,
  author={Anton-Lamprecht, Ingrun},
  title={Recent advances in understanding epidermolysis bullosa},
  year={1995},
  pages={69-72},
  language={eng},
  isbn={0-444-81917-7 and 978-0-444-81917-8},
  booktitle={Pediatric dermatology},
}
@article{UBHD-69124809,
  author={Anton-Lamprecht, Ingrun},
  title={Rezessive Ichthyosis congenita Typ II (Cholesterintyp)},
  year={1996},
  pages={803-804},
  language={ger},
  issn={0301-0481},
  volume={71},
  journal={H + G},
}
@article{UBHD-69131757,
  author={Anton-Lamprecht, Ingrun},
  title={T{\"o}dlich verlaufendes Netherton-Syndrom unter dem Bild einer schweren Erythrodermie mit Hypernatr{\"a}mie bei zwei Geschwistern},
  year={1995},
  pages={40-41},
  language={ger},
  issn={0935-3453},
  volume={7},
  journal={Hautnah},
}
@article{UBHD-69131775,
  author={Anton-Lamprecht, Ingrun},
  title={Ultrastructural identification of basic abnormalities as clues to genetic disorders of the epidermis},
  year={1994},
  pages={S6-S12},
  language={eng},
  issn={1523-1747},
  volume={103},
  note={Elektronische Reproduktion der Druck-Ausgabe 20. Juli 2016 ; Gesehen am 19.10.2023},
  journal={The journal of investigative dermatology},
  doi={10.1038/jid.1994.3},
}
@book{UBHD-1169178,
  author={Anton-Lamprecht, Ingrun},
  title={Zur Ultrastruktur heredit{\"a}rer Verhornungsst{\"o}rungen},
  year={1973},
  pages={Getr. Z{\"a}hlung},
  language={ger},
  note={Enth. 6 Sonderabdr. aus verschiedenen Zeitschr},
  school={Heidelberg, Univ., Habil.-Schr., 1974},
  library={UB ; UB [Signatur: 74 Q 914]},
}
@article{UBHD-69126379,
  author={Blaschke, Sonja and M{\"o}ller, Ronald and Haußer-Siller, Ingrid and Anton-Lamprecht, Ingrun and Paul, Eberhard},
  title={Comèl-Netherton-Syndrom},
  year={1998},
  pages={499-504},
  language={ger},
  issn={1432-1173},
  volume={49},
  number={6},
  note={Gesehen am 04.10.2023},
  journal={Der Hautarzt},
  doi={10.1007/s001050050778},
}
@article{UBHD-67797134,
  author={Brandt, Tobias and Haußer-Siller, Ingrid and Orberk, Erdem and Grau, Armin J. and Hartschuh, Wolfgang and Anton-Lamprecht, Ingrun and Hacke, Werner},
  title={Ultrastructural connective tissue abnormalities in patients with spontaneous cervicocerebral artery dissections},
  year={1998},
  pages={5 S.},
  language={eng},
  issn={1531-8249},
  volume={44},
  note={Gesehen am 31.03.2015},
  journal={Annals of neurology},
  doi={10.1002/ana.410440224},
}
@article{UBHD-69127006,
  author={Chan, Yujia A. and Anton-Lamprecht, Ingrun and Yu, Q. C. and J{\"a}ckel, Andreas and Zabel, B. and Ernst, J. P. and Fuchs, E.},
  title={A human keratin 14 "knockout"},
  subtitle={the absence of K14 leads to severe epidermolysis bullosa simplex and a function for an intermediate filament protein},
  year={1994},
  pages={2574-2587},
  language={eng},
  issn={1549-5477},
  volume={8},
  number={21},
  note={Gesehen am 05.10.2023},
  journal={Genes & development},
  doi={10.1101/gad.8.21.2574},
}
@article{UBHD-69124774,
  author={Christiano, Angela M. and Anton-Lamprecht, Ingrun and Amano, S. and Ebschner, Ulrike and Burgeson, R. E. and Uitto, J.},
  title={Compound heterozygosity for COL7A1 mutations in twins with dystrophic epidermolysis bullosa},
  subtitle={a recessive paternal deletion/insertion mutation and a dominant negative maternal glycine substitution result in a severe phenotype},
  year={1996},
  pages={682-693},
  language={eng},
  issn={0002-9297},
  volume={58},
  number={4},
  journal={American journal of human genetics},
}
@book{UBHD-69124950,
  editor={Korting, G{\"u}nter W.},
  title={Dermatologie in Praxis und Klinik f{\"u}r die fach{\"a}rztliche Weiterbildung},
  subtitle={in 4 B{\"a}nden},
  publisher={Thieme},
  address={Stuttgart},
  year={1979-},
  language={ger},
}
@article{UBHD-69126999,
  author={Gedde-Dahl, Tobias and Dupuy, Bertt Myhre and Jonassen, Reidun and Winberg, Jan-Olof and Anton-Lamprecht, Ingrun and Olalsen, Bjomar},
  title={Junctional epidermolysis bullosa inversa (locus EBR2A) assigned to 1q31 by linkage and association to LAMC1},
  year={1994},
  pages={1387-1391},
  language={eng},
  issn={1460-2083},
  volume={3},
  number={8},
  note={Gesehen am 05.10.2023},
  journal={Human molecular genetics},
  doi={10.1093/hmg/3.8.1387},
}
@article{UBHD-69132594,
  author={Hammami Hauasli, Nadja and Ulrike Kalinke, D. and Schumann, Hauke and Kalinke, Ulrich and Pontz, Bertram F. and Anton-Lamprecht, Ingrun and Pulkkinen, Leena and Zimmermann, Mirjam and Uitto, Jouni and Bruckner-Tuderman, Leena},
  title={A combination of a common splice site mutation and frameshift mutation in the COL7A1 gene},
  subtitle={absence of functional collagen VII in keratinocytes and skin},
  year={1997},
  pages={384-389},
  language={eng},
  issn={1523-1747},
  volume={109},
  number={3},
  note={Elektronische Reproduktion der Druck-Ausgabe 8. Dezember 2015 ; Gesehen am 23.10.2023},
  journal={The journal of investigative dermatology},
  doi={10.1111/1523-1747.ep12336264},
}
@article{UBHD-69126433,
  author={Haußer-Siller, Ingrid and Anton-Lamprecht, Ingrun},
  title={Differential ultrastructural aberrations of collagen fibrils in Ehlers-Danlos syndrome types I-IV as a means of diagnostics and classification},
  year={1994},
  pages={394-407},
  language={eng},
  issn={1432-1203},
  volume={93},
  number={4},
  note={Gesehen am 04.10.2023},
  journal={Human genetics},
  doi={10.1007/BF00201664},
}
@article{UBHD-69124859,
  author={Haußer-Siller, Ingrid and Anton-Lamprecht, Ingrun},
  title={Severe congenital generalized exfoliative erythroderma in newborns and infants},
  subtitle={a possible sign of Netherton syndrome},
  year={1996},
  pages={183-199},
  language={eng},
  issn={1525-1470},
  volume={13},
  number={3},
  note={Gesehen am 27.09.2023},
  journal={Pediatric dermatology},
  doi={10.1111/j.1525-1470.1996.tb01202.x},
}
@article{UBHD-69126383,
  author={K{\"o}nig, Insa and Haußer-Siller, Ingrid and Anton-Lamprecht, Ingrun and Schroeter, Renate and Petzoldt, Detlef},
  title={Hyalinosis cutis et mucosae and Ehlers-Danlos syndrome},
  subtitle={a rare combination of syndromes},
  year={1994},
  pages={108-112},
  language={eng},
  issn={1432-1173},
  volume={45},
  number={2},
  note={Gesehen am 04.10.2023},
  journal={Der Hautarzt},
  doi={10.1007/s001050050049},
}
@article{UBHD-69126432,
  author={Krahl, Dieter and Sigwart, Andrea and Hartschuh, Wolfgang and Anton-Lamprecht, Ingrun and Petzoldt, Detlef},
  title={Erythrokeratolysis hiemalis},
  subtitle={scaling erythematous genodermatosis with seasonal manifestation},
  year={1994},
  pages={776-779},
  language={eng},
  issn={1432-1173},
  volume={45},
  number={11},
  note={Gesehen am 04.10.2023},
  journal={Der Hautarzt},
  doi={10.1007/s001050050170},
}
@article{UBHD-69132567,
  author={Paepe, A. de and Nuytinck, L. and Haußer-Siller, Ingrid and Anton-Lamprecht, Ingrun and Naeyaert, J. M.},
  title={Mutations in the COL5A1 gene are causal in the Ehlers-Danlos syndromes I and II},
  year={1997},
  pages={547-554},
  language={eng},
  issn={0002-9297},
  volume={60},
  number={3},
  journal={American journal of human genetics},
}
@article{UBHD-69131798,
  author={Pigg, Maritta and Gedde-Dahl, Tobias and Cox, Diane and Haußer-Siller, Ingrid and Anton-Lamprecht, Ingrun and Dahl, Niklas},
  title={Strong founder effect for a transglutaminase 1 gene mutation in lamellar ichthyosis and congenital ichthyosiform erythroderma from Norway},
  year={1998},
  pages={589-596},
  language={eng},
  issn={1476-5438},
  volume={6},
  number={6},
  note={Gesehen am 19.10.2023},
  journal={European journal of human genetics},
  doi={10.1038/sj.ejhg.5200224},
}
@article{UBHD-69131795,
  author={Pohl, Martin and Zimmerhackl, Lothar Bernd and Haußer-Siller, Ingrid and Ludwig, H. and Hildebrandt, F. and Gordjani, N. and Sutor, Anton H. and Anton-Lamprecht, Ingrun and Brandis, M.},
  title={Acute bilateral renal vein thrombosis complicating Netherton syndrome},
  year={1998},
  pages={157-160},
  language={eng},
  issn={1432-1076},
  volume={157},
  number={2},
  note={Gesehen am 19.10.2023},
  journal={European journal of pediatrics},
  doi={10.1007/s004310050789},
}
@incollection{UBHD-69125119,
  author={Rauskolb, R{\"u}diger and Anton-Lamprecht, Ingrun},
  title={Pr{\"a}natale Diagnostik von erblichen Hauterkrankungen durch Fetoskopie und Elektronenmikroskopie},
  year={1987},
  pages={80-104},
  language={ger},
  isbn={3-540-16294-1 and 0-387-16294-1 and 978-3-540-16294-0 and 978-0-387-16294-2},
  booktitle={Pr{\"a}natale Medizin},
  editor={Holzgreve, Wolfgang},
}
@article{UBHD-69126376,
  author={Sillén, Anna and Anton-Lamprecht, Ingrun and Braun-Quentin, Cordula and Kraus, Cornelia S. and Sayli, Bekir Sitki and Ayuso, Carmen and Jagell, Sten and K{\"u}ster, Wolfgang and Wadelius, Claes},
  title={Spectrum of mutations and sequence variants in the FALDH gene in patients with Sj{\"o}gren-Larsson syndrome},
  year={1998},
  pages={377-384},
  language={eng},
  issn={1098-1004},
  volume={12},
  number={6},
  note={Elektronische Reproduktion der Druck-Ausgabe 7. Januar 1999 ; Gesehen am 04.10.2023},
  journal={Human mutation},
  doi={10.1002/(SICI)1098-1004(1998)12:6<377::AID-HUMU3>3.0.CO;2-I},
}
@article{UBHD-69124860,
  author={Tinschert, Sigrid and Anton-Lamprecht, Ingrun and Albrecht-Nebe, Helga},
  title={Zunich neuroectodermal syndrome},
  subtitle={migratory ichthyosiform dermatosis, colobomas, and other abnormalities},
  year={1996},
  pages={363-371},
  language={eng},
  issn={1525-1470},
  volume={13},
  number={5},
  note={Gesehen am 27.09.2023},
  journal={Pediatric dermatology},
  doi={10.1111/j.1525-1470.1996.tb00702.x},
}
@article{UBHD-69124864,
  author={Uttam, Jai and Hutton, E. and Coulombe, P. A. and Anton-Lamprecht, Ingrun and Yu, Q. C. and Gedde-Dahl, T. and Fine, J. D. and Fuchs, E.},
  title={The genetic basis of epidermolysis bullosa simplex with mottled pigmentation.},
  year={1996},
  pages={9079-9084},
  language={eng},
  issn={1091-6490},
  volume={93},
  number={17},
  note={Gesehen am 27.09.2023},
  journal={Proceedings of the National Academy of Sciences of the United States of America},
  doi={10.1073/pnas.93.17.9079},
}
@article{UBHD-69127015,
  author={Winberg, Jan-Olof and Anton-Lamprecht, Ingrun and K{\"o}nig, A. and Bruckner-Tuderman, Leena and Nilssen, Odd and Gedde-Dahl, Tobias},
  title={Biochemical, molecular and ultrastructural heterogeneity in severe generalized mutilating recessive dystrophic epidermolysis bullosa hallopeau-siemens},
  year={1994},
  pages={47-54},
  language={eng},
  issn={1167-1122},
  volume={4},
  journal={European journal of dermatology},
}
@article{UBHD-69132574,
  author={Winberg, Jan-Olof and Hammami-Hauasli, Nadja and Nilssen, Øivind and Anton-Lamprecht, Ingrun and Naylor, Susan L. and Kerbacher, Karen and Zimmermann, Mirjam and Krajci, Peter and Gedde-Dahl, Tobias and Bruckner-Tuderman, Leena},
  title={Modulation of disease severity of dystrophic epidermolysis bullosa by a splice site mutation in combination with a missense mutation in the COL7A1 gene},
  year={1997},
  pages={1125-1135},
  language={eng},
  issn={1460-2083},
  volume={6},
  number={7},
  note={Gesehen am 23.10.2023},
  journal={Human molecular genetics},
  doi={10.1093/hmg/6.7.1125},
}