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Journal of Medical Genetics|March 1, 1997
Hereditary spinal neurofibromatosis: a rare form of NF1?M Poyhonen, E L Leisti, S Kytölä, et al.
Acta Paediatrica (Oslo, Norway : 1992)|February 13, 2003
Free sialic acid storage (Salla) disease in SwedenA Erikson, N Aula, P Aula, et al.
Hereditas|April 28, 2000
Origin of Finnish mutations causing aspartylglucosaminuriaS Valkonen, M Hietala, M L Savontaus, et al.
Clinical Genetics|February 1, 1990
Prenatal diagnosis in Pelizaeus-Merzbacher disease using RFLP analysisJ Mäenpää, E Lindahl, P Aula, et al.
Clinical Genetics|August 1, 1985
Partial trisomy 12q: clinical and cytogenetic observationsC Tengström, M Wilska, M Kähkönen, et al.
American Journal of Medical Genetics|October 1, 1984
Prenatal diagnosis and fetal pathology of aspartylglucosaminuriaP Aula, J Rapola, H von Koskull, et al.
Clinical Genetics|June 1, 1978
Incomplete prenatal diagnosis of G-trisomy mosaicismK Simola, P Aula, M Ryynänen, et al.
The Journal of Clinical Investigation|July 1, 1992
Identification of a common mutation in Finnish patients with nonketotic hyperglycinemiaS Kure, M Takayanagi, K Narisawa, et al.
International Journal of Pediatric Otorhinolaryngology|September 1, 1979
Wegener's granulomatosis in childhood. A clinical report based on 3 casesA Backman, B Grahne, E Holopainen, et al.
Prenatal Diagnosis|March 1, 1994
Transabdominal chorionic villus sampling and amniocentesis for prenatal diagnosis: 5 years' experience at a university centreP Palo, O Piiroinen, E Honkonen, et al.
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