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American Journal of Respiratory and Critical Care Medicine|May 12, 2000
Exogenous surfactant kinetics in infant respiratory distress syndrome: A novel method with stable isotopesM Torresin, L J Zimmermann, P E Cogo, et al.Metabolism: Clinical and Experimental|October 1, 1994
Conversion of octanoic acid into long-chain saturated fatty acids in premature infants fed a formula containing medium-chain triglyceridesV P Carnielli, E J Sulkers, C Moretti, et al.Child'S Nervous System : Chns : Official Journal of the International Society for Pediatric Neurosurgery|August 14, 1999
Fibroblast growth factor receptor mutational screening in newborns affected by metopic synostosisM Tartaglia, V Bordoni, F Velardi, et al.Human Genetics|October 30, 1999
CD4 and CD8 T lymphocyte inheritance. Evidence for major autosomal recessive genesM Clementi, P Forabosco, A Amadori, et al.Annales De Genetique|June 1, 1976
[Localization of the gene of the glyceraldehyde 3 phosphate dehydrogenase on the distal segment of the short arm of the chromosome 12]M O Rethoré, C Junien, G Malpuech, et al.La Pediatria Medica E Chirurgica : Medical and Surgical Pediatrics|May 1, 1996
[The evolution of care for the critical child: pediatric intensive care]L Chiandetti, A Pettenazzo, P Biban, et al.Teratology|January 1, 1993
Omphalocele and gastroschisis: a collaborative study of five Italian congenital malformation registriesE Calzolari, S Volpato, F Bianchi, et al.Human Genetics|October 1, 1993
D8S7 is consistently deleted in inverted duplications of the short arm of chromosome 8 (inv dup 8p)A Minelli, G Floridia, E Rossi, et al.Journal of Medical Screening|February 24, 2001
Evaluation of the prenatal diagnosis of neural tube defects by fetal ultrasonographic examination in different centres across EuropeP A Boyd, D G Wellesley, H E De Walle, et al.Human Genetics|January 1, 1985
Frequency of consanguineous marriages among parents and grandparents of Down patientsM Devoto, L Prosperi, F D Bricarelli, et al.Pageof 18