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Maritta Pigg

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Sweden

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Yeast Artificial Chromosomes

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J Dahlqvist; Joakim Klar; Ingrid Hausser; Ingrun Anton-Lamprecht; Maritta Pigg; Tobias Gedde-Dahl; Agneta Gånemo; Anders Vahlquist; Niklas Dahl
Congenital ichthyosis: mutations in ichthyin are associated with specific structural abnormalities in the granular layer of epidermis.
Joakim Klar; Tobias Gedde-Dahl; M Larsson; Maritta Pigg; B Carlsson; Dmitry Tentler; Anders Vahlquist; Niklas Dahl
Assignment of the locus for ichthyosis prematurity syndrome to chromosome 9q33.3-34.13.
Anders Vahlquist; Agneta Gånemo; Maritta Pigg; Marie Virtanen; Per Westermark
The clinical spectrum of congenital ichthyosis in Sweden: a review of 127 cases.

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All Publications

2007: J Dahlqvist; Joakim Klar; Ingrid Hausser; Ingrun Anton-Lamprecht; Maritta Pigg; Tobias Gedde-Dahl; Agneta Gånemo; Anders Vahlquist; Niklas Dahl
Congenital ichthyosis: mutations in ichthyin are associated with specific structural abnormalities in the granular layer of epidermis.
Journal of medical genetics 2007;44(10):615-20.
2004: Joakim Klar; Tobias Gedde-Dahl; M Larsson; Maritta Pigg; B Carlsson; Dmitry Tentler; Anders Vahlquist; Niklas Dahl
Assignment of the locus for ichthyosis prematurity syndrome to chromosome 9q33.3-34.13.
Journal of medical genetics 2004;41(3):208-12.
2003: Anders Vahlquist; Agneta Gånemo; Maritta Pigg; Marie Virtanen; Per Westermark
The clinical spectrum of congenital ichthyosis in Sweden: a review of 127 cases.
Acta dermato-venereologica. Supplementum 2003;(213):34-47.
2003: Agneta Gånemo; Maritta Pigg; Marie Virtanen; Terje Kukk; Heli Raudsepp; Ingrid Rossman-Ringdahl; Per Westermark; Katri Niemi; Niklas Dahl; Anders Vahlquist
Autosomal recessive congenital ichthyosis in Sweden and Estonia: clinical, genetic and ultrastructural findings in eighty-three patients.
Acta dermato-venereologica 2003;83(1):24-30.
2000: Maritta Pigg; Tobias Gedde-Dahl; D W Cox; G Haugen; Niklas Dahl
Haplotype association and mutation analysis of the transglutaminase 1 gene for prenatal exclusion of lamellar ichthyosis.
Prenatal diagnosis 2000;20(2):132-7.
1999: Maritta Pigg; I Annton-Lamprecht; C Braun-Quentin; Karl-Henrik Gustavson; Claes Wadelius
Further evidence of genetic homogeneity in Sjögren-Larsson syndrome.
Acta dermato-venereologica 1999;79(1):41-3.
1998: Maritta Pigg; Tobias Gedde-Dahl; D Cox; Ingrid Hausser; Ingrun Anton-Lamprecht; Niklas Dahl
Strong founder effect for a transglutaminase 1 gene mutation in lamellar ichthyosis and congenital ichthyosiform erythroderma from Norway.
European journal of human genetics : EJHG 1998;6(6):589-96.
1998: A Sillén; A Alderborn; Maritta Pigg; S Jagell; Claes Wadelius
Detailed genetic and physical mapping in the Sjögren-Larsson syndrome gene region in 17p11.2.
Hereditas 1998;128(3):245-50.
1997: Niklas Dahl; Maritta Pigg; E Ristoff; R Gali; B Carlsson; Bengt Mannervik; Agne Larsson; P Board
Missense mutations in the human glutathione synthetase gene result in severe metabolic acidosis, 5-oxoprolinuria, hemolytic anemia and neurological dysfunction.
Human molecular genetics 1997;6(7):1147-52.
1995: Karl-Henrik Gustavson; S Jagell; Maritta Pigg; Claes Wadelius
[From rune stones to genes. The cause of Sjögren-Larsson syndrome is encircled].
Läkartidningen 1995;92(28-29):2748-50.
1995: D Agardi; Maritta Pigg; Anders G Sjöholm; Lennart Truedsson; P J Späth; Ed J Kuijper; C C Tijssen; L Tranebjaerg; Karl-Henrik Gustavson; P J Ulfendahl
Fluorescent detection of microsatellite polymorphisms: properdin deficiency linked to PFC microsatellite.
Experimental and clinical immunogenetics 1995;12(2):111-4.
1994: Maritta Pigg; S Jagell; A Sillén; J Weissenbach; Karl-Henrik Gustavson; Claes Wadelius
The Sjögren-Larsson syndrome gene is close to D17S805 as determined by linkage analysis and allelic association.
Nature genetics 1994;8(4):361-4.
1993: Claes Wadelius; M Lindstedt; Maritta Pigg; N Egberg; Ulf Pettersson; Maria Anvret
Hemophilia B in a 46,XX female probably caused by non-random X inactivation.
Clinical genetics 1993;43(1):1-4.
1992: Claes Wadelius; Maritta Pigg; M Sundvall; Anders G Sjöholm; P Goonewardena; Ed J Kuijper; C C Tijssen; A Jansz; P J Späth; U B Schaad
Linkage analysis in properdin deficiency families: refined location in proximal Xp.
Clinical genetics 1992;42(1):8-12.