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253 results on '"Golbus MS"'

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2. Restriction Enzyme Analysis of Norrie Disease Pedigrees

3. Two-colour immunocytochemical staining of gamma (gamma) and epsilon (epsilon) type haemoglobin in fetal red cells

5. Maternal outcome after open fetal surgery. A review of the first 17 human cases.

6. Effects of Human Chorionic Gonadotropin Preparations on Amino Acid Uptake and Incorporation into Protein in vitro

7. The influence of strain, maternal age, and method of maturation on mouse oocyte aneuploidy

8. Prenatal diagnosis of classic hemophilia (hemophilia A) by immunoradiometric assays

12. Two-colour immunocytochemical staining of gamma (gamma) and epsilon (epsilon) type haemoglobin in fetal red cells.

13. Reproductive Genetic Counseling to Asian-Pacific and Latin American Immigrants.

14. In utero allogeneic hematopoietic stem cell transplantation to induce tolerance.

15. Use of amniotic fluid amino acids in prenatal testing for argininosuccinic aciduria and citrullinaemia.

16. Rapid aneuploid diagnosis of high-risk fetuses by fluorescence in situ hybridization.

17. International, collaborative experience of 1789 patients having multifetal pregnancy reduction: a plateauing of risks and outcomes.

18. Comparison of transcervical and transabdominal chorionic villus sampling loss rates in nine thousand cases from a single center.

19. Fetal muscle biopsy: collaborative experience with varied indications.

20. Desbuquois syndrome: clinical, radiographic, and morphologic characterization.

21. Efficacy of second-trimester selective termination for fetal abnormalities: international collaborative experience among the world's largest centers.

22. Prenatal diagnosis of unusual hemoglobinopathies.

23. The association between 'faint-positive' amniotic fluid acetylcholinesterase and fetal malformations.

24. Growth retardation in prenatally diagnosed cases of gastroschisis.

25. Prenatal diagnosis of hemophilia involving grandpaternal mosaicism.

26. Prenatal diagnosis using fetal cells from the maternal circulation.

27. Stem cell transplantation.

28. Fetal tissue sampling--indications, techniques, complications, and experience with sampling of fetal skin, liver, and muscle.

29. Elevated levels of amniotic fluid alpha-fetoprotein: sonographic evaluation.

30. Efficacy of transabdominal multifetal pregnancy reduction: collaborative experience among the world's largest centers.

31. Prenatal in situ hybridization test for deleted steroid sulfatase gene.

32. Mental retardation locus in Xp21 chromosome microdeletion.

33. Fetal surgery for cystic adenomatoid malformation of the lung.

34. The role of velamentous cord insertion in the etiology of twin-twin transfusion syndrome.

35. Unreliability of platelet glucose-6-phosphatase for the diagnosis of glycogen storage disease type Ia.

36. Isolation and characterization of Y chromosome DNA probes.

37. Cytogenetic evidence for enhanced selective miscarriage of trisomy 21 pregnancies with advancing maternal age.

38. Prenatal diagnosis of Chediak-Higashi syndrome.

39. Outcome of antenatally diagnosed cystic adenomatoid malformations.

40. Prenatal diagnosis of Duchenne muscular dystrophy by fetal muscle biopsy.

41. Maternal serum CA 125 for aneuploidy detection in early pregnancy.

42. Restriction enzyme analysis of Norrie disease pedigrees.

43. A randomized comparison of transcervical and transabdominal chorionic-villus sampling. The U.S. National Institute of Child Health and Human Development Chorionic-Villus Sampling and Amniocentesis Study Group.

44. Prenatal diagnosis with repetitive in situ hybridization probes.

45. In utero stem cell therapy.

46. Cytogenetic results from the U.S. Collaborative Study on CVS.

47. First-trimester biochemical and molecular diagnoses using chorionic villi: high accuracy in the U.S. collaborative study.

48. The Norrie disease gene maps to a 150 kb region on chromosome Xp11.3.

49. Prenatal diagnosis.

50. Risk factors associated with transcervical CVS losses.

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