Wahlström J - Search Results

1

Maternal origin of inv dup(15) chromosomes in infantile autism.

Martinsson T, Johannesson T, Vujic M, Sjöstedt A, Steffenburg S, Gillberg C, Wahlström J. Martinsson T, et al. Among authors: wahlstrom j. Eur Child Adolesc Psychiatry. 1996 Dec;5(4):185-92. doi: 10.1007/BF00538845. Eur Child Adolesc Psychiatry. 1996. PMID: 8989557

2

Autism associated with marker chromosome.

Gillberg C, Steffenburg S, Wahlström J, Gillberg IC, Sjöstedt A, Martinsson T, Liedgren S, Eeg-Olofsson O. Gillberg C, et al. Among authors: wahlstrom j. J Am Acad Child Adolesc Psychiatry. 1991 May;30(3):489-94. doi: 10.1097/00004583-199105000-00022. J Am Acad Child Adolesc Psychiatry. 1991. PMID: 2055888

3

Monozygotic female twins with autism and the fragile-X syndrome (AFRAX).

Gillberg C, Ohlson VA, Wahlström J, Steffenburg S, Blix K. Gillberg C, et al. Among authors: wahlstrom j. J Child Psychol Psychiatry. 1988 Jul;29(4):447-51. doi: 10.1111/j.1469-7610.1988.tb00736.x. J Child Psychol Psychiatry. 1988. PMID: 3215918

4

Congenital variant Rett syndrome in a girl with terminal deletion of chromosome 3p.

Wahlström J, Uller A, Johannesson T, Holmqvist D, Darnfors C, Vujic M, Tonnby B, Hagberg B, Martinsson T. Wahlström J, et al. J Med Genet. 1999 Apr;36(4):343-5. J Med Genet. 1999. PMID: 10227408 Free PMC article.

5

A candidate region for Asperger syndrome defined by two 17p breakpoints.

Tentler D, Johannesson T, Johansson M, Råstam M, Gillberg C, Orsmark C, Carlsson B, Wahlström J, Dahl N. Tentler D, et al. Among authors: wahlstrom j. Eur J Hum Genet. 2003 Feb;11(2):189-95. doi: 10.1038/sj.ejhg.5200939. Eur J Hum Genet. 2003. PMID: 12634868

6

Chromosomes in anorexia nervosa. A study of 47 cases including a population-based group: a research note.

Råstam M, Gillberg C, Wahlström J. Råstam M, et al. Among authors: wahlstrom j. J Child Psychol Psychiatry. 1991 May;32(4):695-701. doi: 10.1111/j.1469-7610.1991.tb00344.x. J Child Psychol Psychiatry. 1991. PMID: 1864897

7

The syndromes described by Kanner and Rett-Hagberg: overlap in an extended family.

Gillberg C, Ehlers S, Wahlström J. Gillberg C, et al. Among authors: wahlstrom j. Dev Med Child Neurol. 1990 Mar;32(3):258-61. doi: 10.1111/j.1469-8749.1990.tb16932.x. Dev Med Child Neurol. 1990. PMID: 2311829

8

Chromosome findings in twins with early-onset autistic disorder.

Wahlström J, Steffenburg S, Hellgren L, Gillberg C. Wahlström J, et al. Am J Med Genet. 1989 Jan;32(1):19-21. doi: 10.1002/ajmg.1320320105. Am J Med Genet. 1989. PMID: 2705478

9

Infantile autism, fragile (X) (q27.3) and RFLP analysis in an extended Swedish family.

Anvret M, Gillberg C, Wahlström J, Albertsson-Wikland K, Davies K. Anvret M, et al. Among authors: wahlstrom j. Clin Genet. 1988 Oct;34(4):265-71. doi: 10.1111/j.1399-0004.1988.tb02874.x. Clin Genet. 1988. PMID: 2906823

10

Chromosome abnormalities in infantile autism and other childhood psychoses: a population study of 66 cases.

Gillberg C, Wahlström J. Gillberg C, et al. Among authors: wahlstrom j. Dev Med Child Neurol. 1985 Jun;27(3):293-304. doi: 10.1111/j.1469-8749.1985.tb04539.x. Dev Med Child Neurol. 1985. PMID: 3160621

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