277 results on '"Dallaire, L."'
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2. Club foot, an adverse outcome of early amniocentesis: disruption or deformation?
3. Deficiency of Fumarylacetoacetase in the Acute Form of Hereditary Tyrosinemia with Reference to Prenatal Diagnosis
4. Trisomy recurrence: A reconsideration based on North American data
5. Confirmation of regional assignment of nucleoside phosphorylase (NP) on chromosome 14 by gene dosage studies
6. Genetic counseling
7. Mendelian and atypical patterns of inheritance
8. Chromosomal disorders - Karyotype indications
9. Neonatal screening
10. Glossary of medical and molecular genetics
11. Prenatal diagnosis
12. PERIPHERAL NERVE FINDINGS IN SENSORIMOTOR CRISES COMPLICATING HEREDITARY HEPATORENAL TYROSINEMIA: 40
13. Recommendations on the use of folic acid supplementation to prevent the recurrence of neural tube defects. Clinical Teratology Committee, Canadian College of Medical Geneticists
14. THYROID ANTIBODIES IN RELATION TO INFECTIOUS HEPATITIS AND DOWN'S SYNDROME
15. Bilateral aniridia, multiple webs and severe mental retardation in a 47, XXY/48, XXXY mosaic
16. Oral and dental development in X chromosome aneuploidy
17. Marqueurs sériques et diagnostic prénatal de la trisomie 21.
18. Prevalence of congenital anomalies at birth among offspring of women at risk for a genetic disorder and with a normal second-trimester ultrasound
19. Fetal congenital diaphragmatic hernia: accuracy of sonography in the diagnosis and prediction of the outcome after birth.
20. Prenatal diagnosis of smith–lemli–opitz syndrome is possible by measurement of 7-dehydrocholesterol in amniotic fluid
21. Parental reaction and adaptability to the prenatal diagnosis of fetal defect or genetic disease leading to pregnancy interruption
22. Is selective abortion for a genetic disease an issue for the medical profession? A comparative study of Quebec and France
23. Phosphate transport by capillaries of the blood-brain barrier.
24. Annex 6: Chromosome mosaicism in CVS and amniocentesis samples
25. Annex 5: List of all cytogenetic abnormalities detected
26. Annex 8: Familial chromosomal aberrations and metabolic disorders
27. Prenatal diagnosis of fetal anomalies during the second trimester of pregnancy: Their characterization and delineation of defects in pregnancies at risk
28. Purification and characterization of metabolically active capillaries of the blood-brain barrier
29. Amniotic Fluid α-Galactosidase Activity: an Indicator of Gestational Age.
30. Oral and dental development in X chromosome aneuploidy.
31. Prenatal detection of intestinal obstruction: deficient amniotic fluid disaccharidases in affected fetuses.
32. Total parenteral nutrition in very low birth weight infants with Travasol 10% blend C.
33. Prenatal identification of a 45,X/46,Xder(Y) mosaicism and confirmation by high resolution cytogenetics and fluorescence in situ hybridization.
34. Familial chromosomal aberrations and metabolic disorders.
35. Canadian multicenter randomized clinical trial of chorion villus sampling and amniocentesis. chromosome mosaicism in CVS and amniocentesis samples.
36. Synchronization of amniotic fluid cells for high resolution cytogenetics.
37. Prenatal diagnosis of trisomy 10 p in a twin pregnancy.
38. Maternal alphafetoproteln screening by the polypropylene tube immunoradiometric assay on dried blood.
39. Separation of amniotic fluid cell types in primary culture by percoll density gradient centrifugation.
40. Prenatal diagnosis of hereditary tyrosinaemia: measurement of succinylacetone in amniotic fluid.
41. Section 3: Prenatal screening and diagnosis of open neural tube defects.
42. Prenatal detection of the autosomal recessive type of polycystic kidney disease by trehalase assay in amniotic fluid.
43. Short communications prenatal detection of the autosomal recessive type of polycystic kidney disease by trehalase assay in amniotic fluid.
44. ORIGIN OF AMNIOCENTESIS-INDUCED RISES OF ALPHA-FETOPROTEIN CONCENTRATIONS IN MATERNAL SERUM.
45. FETO-MATERNAL AMINO ACID METABOLISM.
46. Syndrome of retardation with urogenital and skeletal anomalies (Smith-Lemli-Opitz syndrome): clinical features and mode of inheritance.
47. Bilateral aniridia, multiple webs and severe mental retardation in a 47, XXY/48, XXXY mosaic.
48. THYROID ANTIBODIES IN RELATION TO INFECTIOUS HEPATITIS AND DOWN'S SYNDROME.
49. Origin and developmental patterns of lactase and other glycosidases in sheep amniotic and allantoic fluid
50. Occurrence and Properties of Fetal Intestinal Glycosidases (Disaccharidases) in Human Amniotic Fluid
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