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Annales De Genetique|December 1, 1976
Mapping of the gene for glutathione reductase on chromosome 8A de la Chapelle, A Icen, P Aula, et al.Prenatal Diagnosis|March 1, 1984
Amniotic fluid pregnancy-specific beta 1-glycoprotein (SP1) in fetal developmental disordersM Heikinheimo, H Jalanko, J Leisti, et al.American Journal of Medical Genetics|January 1, 1986
Second trimester prenatal diagnosis of the fragile XN Tommerup, P Aula, B Gustavii, et al.Kidney International|March 1, 1997
Improved prenatal diagnosis of the congenital nephrotic syndrome of the Finnish type based on DNA analysisM Männikkö, M Kestilä, U Lenkkeri, et al.Human Genetics|September 12, 2000
An unexpected recurrence of Angelman syndrome suggestive of maternal germ-line mosaicism of del(15)(q11q13) in a Finnish familyH Kokkonen, J LeistiClinical Genetics|February 1, 1977
Morphology of the placenta in fetal I-cell diseaseJ Rapola, P AulaJournal of Perinatal Medicine|January 1, 1982
Heart rate patterns in trisomic fetusesV Kariniemi, P AulaAnnales Chirurgiae Et Gynaecologiae Fenniae|January 1, 1975
Intrauterine diagnosis of chromosome anomaliesO Karjalainen, P AulaBritish Medical Journal (Clinical Research Ed.)|May 29, 1982
Decrease in gamma-glutamyl transpeptidase activity in early amniotic fluid in fetal trisomy 18 syndromeH Janlanko, P AulaPageof 17