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1

Identification of mutations in the CACNL1A3 gene in 13 families of Scandinavian origin having hypokalemic periodic paralysis and evidence of a founder effect in Danish families

Sillén, Anna, Sørensen, Troels, Kantola, Ilkka, Friis, Mogens Laue, Gustavson, Karl-Henrik, Wadelius, Claes

Journal:

American Journal of Medical Genetics

Year:

1997

Language:

english

File:

PDF, 136 KB

english, 1997

2

Fragile X families in a Northern Swedish county - a genealogical study demonstrating apparent paternal transmission from the 18th century

Gösta Holmgren, Hans K. Son Blomquist, Ulf Drugge, Karl-Henrik Gustavson

Journal:

American Journal of Medical Genetics Part A

Year:

1988

Language:

english

File:

PDF, 276 KB

english, 1988

3

Study of individuals possibly affected with the fragile X syndrome in a large swedish family in the 18th to 20th centuries

Ulf Drugge, GöSta Holmgren, Hans Kison Blomquist, Niklas Dahl, Karl-Henrik Gustavson, Helena Malmgren

Journal:

American Journal of Medical Genetics Part A

Year:

1992

Language:

english

File:

PDF, 157 KB

english, 1992

4

Dredging processes and remedy effectiveness: Relationship to the 4 Rs of environmental dredging

Todd S Bridges, Karl E Gustavson, Paul Schroeder, Stephen J Ells, Donald Hayes, Steven C Nadeau, Michael R Palermo, Clay Patmont

Journal:

Integrated Environmental Assessment and Management

Year:

2010

Language:

english

File:

PDF, 367 KB

english, 2010

5

Evaluating the Effectiveness of Contaminated-Sediment Dredging

Francingues, Karl E. Gustavson, G. Allen Burton, , Wolfe, Jr., Danny D. Reible, Donna J. Vorh

Journal:

Environmental Science & Technology

Year:

2008

Language:

english

File:

PDF, 1.66 MB

english, 2008

6

Clustering of private mutations in the congenital chloride diarrhea/down-regulated in adenoma gene

Pia Höglund, Siru Haila, Karl-Henrik Gustavson, Mikko Taipale, Katariina Hannula, Kataryna Popinska, Christer Holmberg, Jerzy Socha, Albert de la Chapelle, Juha Kere

Journal:

Year:

1998

Language:

english

File:

PDF, 201 KB

english, 1998

7

Friedreich's ataxia: Point mutations and clinical presentation of compound heterozygotes

Mireille Cossée, Alexandra Dürr, Michèle Schmitt, Niklas Dahl, Paul Trouillas, Patricia Allinson, Markus Kostrzewa, Annie Nivelon-Chevallier, Karl-Henrik Gustavson, Alfried Kohlschütter, Ulrich Müller

Journal:

Annals of Neurology

Year:

1999

Language:

english

File:

PDF, 152 KB

english, 1999

8

Infantile autism and the fragile X. A swedish multicenter study

Jan Wahlström, Christopher Gillberg, Karl-Henrik Gustavson, Gösta Holmgren, John M. Opitz, James F. Reynolds

Journal:

American Journal of Medical Genetics Part A

Year:

1986

Language:

english

File:

PDF, 256 KB

english, 1986

9

Prevalence of the fragile-X syndrome in mentally retarded boys in a Swedish county

Karl-Henrik Gustavson, Hans Blomquist K:son, Gösta Holmgren, John M. Opitz, James F. Reynolds

Journal:

American Journal of Medical Genetics Part A

Year:

1986

Language:

english

File:

PDF, 268 KB

english, 1986

10

Growth retardation in Down syndrome in relation to insulin-like growth factors and growth hormone

Göran Annerén, Karl-Henrik Gustavson, Vicki R. Sara, Torsten Tuvemo

Journal:

American Journal of Medical Genetics Part A

Year:

1990

Language:

english

File:

PDF, 414 KB

english, 1990

11

Carrier detection of the fragile X syndrome using flanking loci DXS98, DXS105, and DXS304

Niklas Dahl, Helena Malmgren, Ulf Pettersson, Gösta Holmgren, Eva Seemanová, Karl-Henrik Gustavson

Journal:

American Journal of Medical Genetics Part A

Year:

1991

Language:

english

File:

PDF, 275 KB

english, 1991

12

Fragile X families in a Northern Swedish County: A genealogical study of possibly affected individuals in the nineteenth century

Ulf Drugge, Hans K:son Blomquist, Karl-Henrik Gustavson, Gösta Holmgren

Journal:

American Journal of Medical Genetics Part A

Year:

1991

Language:

english

File:

PDF, 364 KB

english, 1991

13

Methylation and mutation patterns in the fragile X syndrome

Helena Malmgren, Marie-Louise Steén-Bondeson, Karl-Henrik Gustavson, Eva Seémanova, Gösta Holmgren, Isabelle Oberlé, Jean-Louis Mandel, Ulf Pettersson, Niklas Dahl

Journal:

American Journal of Medical Genetics Part A

Year:

1992

Language:

english

File:

PDF, 749 KB

english, 1992

14

Infantile autism—fragile X: Molecular findings support genetic heterogeneity

Helena Malmgren, Karl-Henrik Gustavson, Jan Wahlström, Ingrid Arpi-Henriksson, Jurgen Bensch, Ulf Pettersson, Dr. Niklas Dahl

Journal:

American Journal of Medical Genetics Part A

Year:

1992

Language:

english

File:

PDF, 353 KB

english, 1992

15

New X-linked syndrome with severe mental retardation, severely impaired vision, severe hearing defect, epileptic seizures, spasticity, restricted joint mobility, and early death

Karl-Henrik Gustavson, Göran Annerén, Helena Malmgren, Niklas Dahl, Carl-Gustaf Ljunggren, Hans Bäckman

Journal:

American Journal of Medical Genetics Part A

Year:

1993

Language:

english

File:

PDF, 857 KB

english, 1993

16

Comparison of toxicities and mechanism of action of n-alkanols in the submitochondrial particle and the Vibrio fischeri bioluminescence (Microtox®) bioassay

Karl E. Gustavson, Anders Svenson, John M. Harkin

Journal:

Environmental Toxicology and Chemistry

Year:

1998

Language:

english

File:

PDF, 83 KB

english, 1998

17

Comparisons of human-cell-based and submitochondrial particle bioassay responses to the MEIC compounds in reference to human toxicity data

Karl E Gustavson, Harry W Read, John M Harkin

Journal:

Year:

2002

Language:

english

File:

PDF, 446 KB

english, 2002

18

Complex aetiology of an apparently Mendelian form of Mental Retardation

Ana Beleza-Meireles, Ingrid Kockum, Qiu-Ping Yuan, Simone Picelli, Lennart Wetterberg, Karl-Henrik Gustavson, Martin Schalling

Journal:

BMC Medical Genetics

Year:

2008

Language:

english

File:

PDF, 1.33 MB

english, 2008

19

Mutation analysis for prenatal diagnosis and heterozygote detection of Gaucher disease type III (norrbottnian type)

Dr Niklas Dahl, Claes Wadelius, Göran Annerén, Karl-Henrik Gustavson

Journal:

Prenatal Diagnosis

Year:

1992

Language:

english

File:

PDF, 357 KB

english, 1992

20

Letter to the editors

Arne Brun, Karl-Henrik Gustavson

Journal:

Year:

1982

Language:

english

File:

PDF, 46 KB

english, 1982

21

Risk factors for mortality in young children living under various socio-economic conditions in Lahore, Pakistan: with particular reference to inbreeding

Muhammad Yaqoob, Sven Cnattingius, Fehmida Jalil, Shakila Zaman, Lennart Iselius, Karl-Henrik Gustavson

Journal:

Clinical Genetics

Year:

1998

Language:

english

File:

PDF, 706 KB

english, 1998

22

The Sjögren-Larsson Syndrome gene is close to D17S805 as determined by linkage analysis and allelic association

Pigg, Maritta, Jagell, Sten, Sillén, Anna, Weissenbach, Jean, Gustavson, Karl-Henrik, Wadelius, Claes

Journal:

Nature Genetics

Year:

1994

File:

PDF, 423 KB

1994

23

Loss of ZDHHC15 expression in a woman with a balanced translocation t(X;15)(q13.3;cen) and severe mental retardation

Mansouri, Mahmoud Reza, Marklund, Lena, Gustavsson, Peter, Davey, Edward, Carlsson, Birgit, Larsson, Catharina, White, Irene, Gustavson, Karl-Henrik, Dahl, Niklas

Journal:

European Journal of Human Genetics

Year:

2005

Language:

english

File:

PDF, 297 KB

english, 2005

24

Mutations in the Heparan-Sulfate Proteoglycan Glypican 6 (GPC6) Impair Endochondral Ossification and Cause Recessive Omodysplasia

Ana Belinda Campos-Xavier, Danielle Martinet, John Bateman, Dan Belluoccio, Lynn Rowley, Tiong Yang Tan, Alica Baxová, Karl-Henrik Gustavson, Zvi U. Borochowitz, A. Micheil Innes, Sheila Unger, Jacque

Journal:

The American Journal of Human Genetics

Year:

2009

Language:

english

File:

PDF, 1.17 MB

english, 2009

25

Treatment of Experimental Acute Mercury Poisoning by Chelating Agents BAL and EDTA

JON GLÖMME, KARL HENRIK GUSTAVSON

Journal:

Journal of Internal Medicine

Year:

1959

Language:

english

File:

PDF, 1.85 MB

english, 1959

26

THE PATTERN OF DNA SYNTHESIS IN HUMAN CHROMOSOMES IN CELLS WITH AN XXY SEX CHROMOSOME CONSTITUTION

LEONARD ATKINS, KARL-HENRIK GUSTAVSON

Journal:

Year:

1964

Language:

english

File:

PDF, 2.02 MB

english, 1964

27

A fragile secondary constriction on chromosome 2 in five patients with different clinical features

GÖRAN ANNERÉN, KARL-HENRIK GUSTAVSON

Journal:

Year:

1981

Language:

english

File:

PDF, 383 KB

english, 1981

28

Trisomy 22 syndrome in a 26-year-old female—A follow-up examination

GöRAN ANNERÉN, KARL-HENRIK GUSTAVSON

Journal:

Year:

1981

Language:

english

File:

PDF, 404 KB

english, 1981

29

Partial trisomy for the distal part of chromosome 22 (22q12→qter) in a mentally retarded girl with congenital birth defects

GÖRAN ANNERÉN, KARL-HENRIK GUSTAVSON, STEN JAGELL

Journal:

Year:

1984

Language:

english

File:

PDF, 741 KB

english, 1984

30

Cytogenetical investigations in patients with primary hyper-parathyroidism and multiple endocrine neoplasia type 1

LARS BENSON, KARL-HENRIK GUSTAVSON, JONAS RASTAD, GORAN ÅKERSTROM, KJELL ÖBERG, SVERKER LJUNGHALL

Journal:

Year:

1988

Language:

english

File:

PDF, 244 KB

english, 1988

31

Prevalence and aetiology of congenital birth defects, infant mortality and mental retardation in Lahore, Pakistan: A prospective cohort study

Karl-Henrik Gustavson

Journal:

Acta Paediatrica

Year:

2005

Language:

english

File:

PDF, 142 KB

english, 2005

32

Congenital glaucoma resulting from a chromosomal translocation

Karl-Henrik Gustavson, Lennart Berggren, Björn Svedberg, Per Törnquist

Journal:

Acta Ophthalmologica (Blackwell)

Year:

1992

Language:

english

File:

PDF, 330 KB

english, 1992

33

Effect of folic acid treatment in the fragile X syndrome

Karl-Henrik Gustavson, Kate Dahlbom, Anders Flood, Gösta Holmgren, Hans K→son Blomquist, Gunnar Sanner

Journal:

Clinical Genetics

Year:

1985

Language:

english

File:

PDF, 294 KB

english, 1985

34

Lethal and non-lethal diastrophic dysplasia A study of 14 Swedish cases

Karl-Henrik Gustavson, Gösta Holmgren, Sten Jagell, Håkan Jorulf

Journal:

Clinical Genetics

Year:

1985

Language:

english

File:

PDF, 894 KB

english, 1985

35

Mental retardation in a North Swedish isolate

Karl-Henrik Gustavson, Lennart Wetterberg, Krystyna Modrzewska

Journal:

Clinical Genetics

Year:

1986

Language:

english

File:

PDF, 447 KB

english, 1986

36

Relative effect of parental birth weight on infant birth weight at term

Jens Langhoff-Roos, Gunilla Lindmark, Karl-Henrik Gustavson, Mehari Gebre-Medhin, Olav Meirik

Journal:

Clinical Genetics

Year:

1987

Language:

english

File:

PDF, 484 KB

english, 1987

37

A new type of muscular dystrophy in two brothers: analysis by use of DNA probes suggests autosomal recessive inheritance

Ponmani Goonewardena, Karl-Henrik Gustavson, Ingrid Gamstorp, Nils-Rune Lundström, Ulf Pettersson

Journal:

Clinical Genetics

Year:

1988

Language:

english

File:

PDF, 453 KB

english, 1988

38

Familial partial trisomy 5p resulting from segregation of an insertional translocation

Karl-Henrik Gustavson, Per Olov Lundberg, Peter Nicol

Journal:

Clinical Genetics

Year:

1988

Language:

english

File:

PDF, 432 KB

english, 1988

39

The prevention and management of autosomal recessive conditions. Main example: alpharantitrypsin deficiency

Karl-Henrik Gustavson

Journal:

Clinical Genetics

Year:

1989

Language:

english

File:

PDF, 366 KB

english, 1989

40

X-linked myotubular myopathy: a linkage study

Catarina Darnfors, H. E. Börje Larsson, Anders Oldfors, Mårten Kyllerman, Karl-Henrik Gustavson, Gunnar Bjursell, Jan Wahlström

Journal:

Clinical Genetics

Year:

1990

Language:

english

File:

PDF, 321 KB

english, 1990

41

Multiplex PCR excludes Duchenne muscular dystrophy in a twin pregnancy

Claes Wadelius, Göran Annéren, Niklas Dahl, Gösta Holmgren, Karl-Henrik Gustavson

Journal:

Clinical Genetics

Year:

1991

Language:

english

File:

PDF, 189 KB

english, 1991

42

The gene for Best's macular dystrophy is located at 11q13 in a Swedish family

Kristina Forsman, Caroline Graff, Stefan Nordström, Kent Johansson, Eleonora Westermark, Erik Lundgren, Karl-Henrik Gustavson, Claes Wadelius, Gösta Holmgren

Journal:

Clinical Genetics

Year:

1992

Language:

english

File:

PDF, 392 KB

english, 1992

43

Repeatability of the Submitochondrial Particle Assay

Francis G. Doherty, Karl E. Gustavson

Journal:

Ecotoxicology and Environmental Safety

Year:

2002

Language:

english

File:

PDF, 124 KB

english, 2002

44

Fine Mapping of Best's Macular Dystrophy Localizes the Gene in Close Proximity to but Distinct from the D11S480/ROM1 Loci

Caroline Graff, Kristina Forsman, Catharina Larsson, Stefan Nordström, Lisbet Lind, Kent Johansson, Ola Sandgren, Jean Weissenbach, Gösta Holmgren, Karl-Henrik Gustavson, Claes Wadelius

Journal:

Year:

1994

File:

PDF, 674 KB

1994

45

Autosomal dominant cerebellar ataxia deafness and narcolepsy

Atle Melberg, Jerker Hetta, Niklas Dahl, Inger Nennesmo, Mats Bengtsson, Rolf Wibom, Crawford Grant, Karl Henrik Gustavson, Per Olov Lundberg

Journal:

Journal of the Neurological Sciences

Year:

1995

Language:

english

File:

PDF, 3.74 MB

english, 1995

46

Chronic myelocytic leukemia with mirror image duplication of chromosome 22: 46,XY,9q+, −22, +t(22q−;22q−)

Karl-Henrik Gustavson, Hans Levander

Journal:

Cancer Genetics and Cytogenetics

Year:

1985

Language:

english

File:

PDF, 256 KB

english, 1985

47

Benign ovarian teratomas: An analysis of their cellular origin

Niklas Dahl, Karl-Henrik Gustavson, Curt Rune, Inger Gustavsson, Ulf Pettersson

Journal:

Cancer Genetics and Cytogenetics

Year:

1990

Language:

english

File:

PDF, 515 KB

english, 1990

48

Elevation of TSH during the early neonatal period

Staffan Engberg, Karl-Henrik Gustavson, Lennart Jacobsson, Ruzena Söderström

Journal:

The Journal of Pediatrics

Year:

1978

Language:

english

File:

PDF, 89 KB

english, 1978

49

Chronic recurrent multifocal osteomyelitis and pustulosis palmoplantaris

Bengt Björkstén, Karl-Henrik Gustavson, Stefan Nordström, Bengt Eriksson, ke Lindholm

Journal:

The Journal of Pediatrics

Year:

1978

Language:

english

File:

PDF, 408 KB

english, 1978

50

On the diagnosis of hypothyroidism in the early neonatal period

Staffan Engberg, Karl-Henrik Gustavson, L. Jacobsson, Ruzena Söderström

Journal:

The Journal of Pediatrics

Year:

1978

Language:

english

File:

PDF, 156 KB

english, 1978