Showing results (71-80 of 161) with videos related to
Sort By:
Pageof 17
Prenatal Diagnosis|September 1, 1989
First-trimester prenatal diagnosis of aspartylglucosaminuriaP Aula, K Mattila, O Piiroinen, et al.Proceedings of the National Academy of Sciences of the United States of America|February 1, 1984
Regional assignment of the structural gene for human alpha-L-iduronidaseE H Schuchman, K H Astrin, P Aula, et al.Human Genetics|October 1, 1988
A new RFLP with StuI and probe cX55.7 (DXS105) and its usefulness in carrier analysis of fragile X syndromeA M Rekilä, M L Väisänen, M Kähkönen, et al.British Medical Journal (Clinical Research Ed.)|August 11, 1984
Risk of minor and major fetal malformations in diabetics with high haemoglobin A1c values in early pregnancyK Ylinen, P Aula, U H Stenman, et al.Journal of Medical Genetics|January 1, 1995
Lethal congenital contracture syndrome (LCCS), a fetal anterior horn cell disease, is not linked to the SMA 5q locusK Vuopala, P Mäkelä-Bengs, A Suomalainen, et al.Human Genetics|January 1, 1992
Exclusion map of Salla disease: attempts to localize the disease gene using a computer programL Haataja, J Schleutker, M Renlund, et al.American Journal of Medical Genetics|March 17, 1997
New progeroid disorderM Penttinen, K M Niemi, H Vinkka-Puhakka, et al.The Journal of Clinical Investigation|April 1, 1991
Sialic acid storage diseases. A multiple lysosomal transport defect for acidic monosaccharidesG M Mancini, C E Beerens, P P Aula, et al.Genomics|November 1, 1990
Analysis of mitochondrial ND4 gene DNA sequence in Finnish families with Leber hereditary optic neuroretinopathyK Huoponen, J Vilkki, M L Savontaus, et al.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.Pageof 17