175 related articles for article (PubMed ID: 4252521)
21. A method for the prenatal diagnosis of the Lesch-Nyhan syndrome using fresh amniotic cells.
Berman PH; Balis ME; Dancis J
Trans Am Neurol Assoc; 1969; 94():222-4. PubMed ID: 5374441
[No Abstract] [Full Text] [Related]
22. Pediatric neurology.
Baird HW
Prog Neurol Psychiatry; 1969; 24():241-54. PubMed ID: 4244101
[No Abstract] [Full Text] [Related]
23. Prenatal genetic diagnosis. 3.
Milunsky A; Littlefield JW; Kanvfer JN; Kolodny EH; Shih VE; Atkins L
N Engl J Med; 1970 Dec; 283(27):1498-504. PubMed ID: 4992307
[No Abstract] [Full Text] [Related]
24. [Current problems of juvenile feeblemindedness].
Steinkopff E
Z Arztl Fortbild (Jena); 1966 Sep; 60(17):989-94. PubMed ID: 4231816
[No Abstract] [Full Text] [Related]
25. [Systematic detection of hereditary metabolic encephalopathies].
Neimann N; Pierson M; Vidailhet M; Siest G; Badonnel Y; Humbel R; Roos F
Ann Pediatr (Paris); 1968 Oct; 15(10):635-41. PubMed ID: 4237831
[No Abstract] [Full Text] [Related]
26. [Examination of newborn children since 1965 in North Rhine-Westphalia for the prevention of phenylketonuria nnd other, hereditary metabolism dependent mental retardations].
Menne F
Offentl Gesundheitswes; 1970 Oct; 32(10):548-50. PubMed ID: 4249843
[No Abstract] [Full Text] [Related]
27. Public health aspects of prenatal diagnosis.
Carter CO
Proc R Soc Med; 1974 Dec; 67(12 Pt 1):1257-8. PubMed ID: 4281086
[No Abstract] [Full Text] [Related]
28. Diagnosis and prenatal diagnosis of lysosomal storage diseases.
Shi HP; Guo YF; Zhang WM; Yuan LF; Luo HY; Sun NH; Zhao SM; Zhu MG
Chin Med J (Engl); 1988 Jun; 101(6):383-7. PubMed ID: 3146466
[No Abstract] [Full Text] [Related]
29. Prevention of hereditary disease.
Jenkins T
S Afr Med J; 1974 Jul; 48(35):1500-6. PubMed ID: 4277615
[No Abstract] [Full Text] [Related]
30. Prospects for the prevention of genetic disease.
Danks DM
Med J Aust; 1973 Mar; 1(12):573-7. PubMed ID: 4267046
[No Abstract] [Full Text] [Related]
31. [Prenatal brain damage in maternal, untreated phenylketonuria].
Peters WH; Lubs H; Machill G; Knapp A; Pietsch P; Wiechert P
Zentralbl Gynakol; 1975; 97(15):905-17. PubMed ID: 1189770
[TBL] [Abstract][Full Text] [Related]
32. Intrauterine diagnosis of congenital and genetic abnormalities.
Cortner JA
J Ark Med Soc; 1972 Nov; 69(6):178-81. PubMed ID: 4263777
[No Abstract] [Full Text] [Related]
33. Biochemical factors in mental retardation.
Hsia DY
Proc Annu Meet Am Psychopathol Assoc; 1967; 56():28-44. PubMed ID: 4966303
[No Abstract] [Full Text] [Related]
34. Ganglioside storage diseases.
O'Brien JS; Okada S; Ho MW; Fillerup DL; Veath ML; Adams K
Fed Proc; 1971; 30(3):956-69. PubMed ID: 4252532
[No Abstract] [Full Text] [Related]
35. Prenatal diagnosis.
Polani PE; Benson PF
Guys Hosp Rep; 1973; 122(1-2):65-89. PubMed ID: 4613622
[No Abstract] [Full Text] [Related]
36. Phenylketonuria.
Hudson FP
Proc R Soc Med; 1967 Nov; 60(11 Part 1):1152-5. PubMed ID: 6060715
[No Abstract] [Full Text] [Related]
37. The prenatal diagnosis of inborn errors of metabolism.
Milunsky A; Littlefield JW
Annu Rev Med; 1972; 23():57-76. PubMed ID: 4264784
[No Abstract] [Full Text] [Related]
38. Inborn errors of metabolism: principles and their applications.
Pinksy L
Can Med Assoc J; 1972 Mar; 106(6):677 passim. PubMed ID: 4551928
[No Abstract] [Full Text] [Related]
39. [Study of the amniotic fluid and its current importance in obstetrics].
Landes P
Sem Hop; 1974 May; 50(23):1577-80. PubMed ID: 4369678
[No Abstract] [Full Text] [Related]
40. New frontiers in paediatrics. Looking at handicapped children today.
Jolly H; Wolff OH
Trans Med Soc Lond; 1971; 87():14-22. PubMed ID: 4262987
[No Abstract] [Full Text] [Related]
[Previous] [Next] [New Search]