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American Journal of Human Genetics|March 1, 1991
Optic atrophy in Leber hereditary optic neuroretinopathy is probably determined by an X-chromosomal gene closely linked to DXS7J Vilkki, J Ott, M L Savontaus, et al.
American Journal of Human Genetics|June 1, 1991
A new mtDNA mutation associated with Leber hereditary optic neuroretinopathyK Huoponen, J Vilkki, P Aula, et al.
The Journal of Clinical Investigation|November 1, 1981
Cultured human amniotic fluid cells characterized with antibodies against intermediate filaments in indirect immunofluorescence microscopyI Virtanen, H von Koskull, V P Lehto, et al.
Obstetrics and Gynecology|June 1, 1981
Prenatal diagnosis of the Meckel syndromeO Karjalainen, P Aula, M Seppälä, et al.
The American Journal of Medicine|August 1, 1975
Lysinuric protein intoleranceO Simell, J Perheentupa, J Rapola, et al.
Lancet (London, England)|October 15, 1977
Association of postmedication hypocortisolism with early first relapse of idiopathic nephrotic syndromeS Leisti, N Hallman, O Koskimies, et al.
The American Review of Respiratory Disease|February 1, 1990
Bronchial epithelial inflammation in children with chronic cough after early lower respiratory tract illnessM Heino, K Juntunen-Backman, M Leijala, et al.
Prenatal Diagnosis|July 27, 1999
Prenatal diagnosis of variant late infantile neuronal ceroid lipofuscinosis (vLINCL[Finnish]; CLN5)J Rapola, J Lähdetie, J Isosomppi, et al.
Clinical Genetics|August 1, 1985
Duchenne-like muscular dystrophy in two sisters with normal karyotypes: evidence for autosomal recessive inheritanceH Somer, A Voutilainen, S Knuutila, et al.
Human Pathology|December 1, 1986
Production of basement membrane laminin and type IV collagen by tumors of striated muscle: an immunohistochemical study of rhabdomyosarcomas of different histologic types and a benign vaginal rhabdomyomaH Autio-Harmainen, M Apaja-Sarkkinen, J Martikainen, et al.
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