145 related articles for article (PubMed ID: 5262932)
1. Fetal cells to spot HEREDITARY DISORDERS.
Am Fam Physician GP; 1970 Feb; 1(2):91. PubMed ID: 5262932
[No Abstract] [Full Text] [Related]
2. Intra-uterine detection of hereditary metabolic disorders.
Nurs Mirror Midwives J; 1970 Feb; 130(7):32. PubMed ID: 5198939
[No Abstract] [Full Text] [Related]
3. Intrauterine diagnosis of fetal disorders.
Kaback MM; Cooke RE
Paediatr Univ Tokyo; 1970 Dec; 18():79-87. PubMed ID: 5535256
[No Abstract] [Full Text] [Related]
4. [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]
5. [Prenatal prediction of congenital errors and malformations].
Llusia DJ
An R Acad Nac Med (Madr); 1975; 92(3):447-66. PubMed ID: 1174295
[No Abstract] [Full Text] [Related]
6. [Gamma-glutamyltransferase activity in amniotic fluid in fetuses with chromosome abnormalities and hereditary metabolic defects].
Macek M; Gustavson KH; Held K; Tomásová H; Hronková J; Burjanková J; Hrycejová I
Cesk Pediatr; 1987 Oct; 42(10):577-82. PubMed ID: 2892588
[No Abstract] [Full Text] [Related]
7. Perinatal diagnosis of the inborn errors of metabolism.
Elsas LJ
J Med Assoc Ga; 1971 Sep; 60(9):308-11. PubMed ID: 5093796
[No Abstract] [Full Text] [Related]
8. Prenatal laboratory diagnosis of hereditary disorders. Amniocentesis and fibroblast tissue culture permit in utero diagnosis of hereditary metabolic disorders.
Perl DP
R I Med J; 1971 Oct; 54(10):509-12. PubMed ID: 4255433
[No Abstract] [Full Text] [Related]
9. The use of amniocentesis for prenatal genetic counseling.
Gertner M; Hsu LY; Martin J; Hirshhorn K
Bull N Y Acad Med; 1970 Nov; 46(11):916-21. PubMed ID: 5273905
[No Abstract] [Full Text] [Related]
10. 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]
11. Newer procedures in the preconceptional, prenatal and early postnatal diagnosis of birth defects.
Nadler HL
Birth Defects Orig Artic Ser; 1970 May; 6(1):26-33. PubMed ID: 5522716
[No Abstract] [Full Text] [Related]
12. [Importance and current possibilities of prenatal diagnosis of genetically conditioned pathologic states].
Srsen S
Cesk Pediatr; 1971 May; 26(5):240-2. PubMed ID: 5559528
[No Abstract] [Full Text] [Related]
13. Prenatal diagnosis in the prevention of genetic disease.
Howell RR; Moore CM
Tex Med; 1974 May; 70(5):77-84. PubMed ID: 4830336
[No Abstract] [Full Text] [Related]
14. [Prenatal diagnosis in medical genetics].
Dallaire L; Pinsky L; Kinch RA; Winsberg F
Union Med Can; 1971 Nov; 100(11):2213-22. PubMed ID: 5170163
[No Abstract] [Full Text] [Related]
15. [Experimental and prenatal diagnosis of lysosomal storage diseases].
Shi HP
Zhonghua Yi Xue Za Zhi; 1988 Mar; 68(3):124-7, 10. PubMed ID: 3136887
[No Abstract] [Full Text] [Related]
16. Prenatal detection of genetic defects.
Nadler HL
J Pediatr; 1969 Jan; 74(1):132-43. PubMed ID: 4882540
[No Abstract] [Full Text] [Related]
17. Genetic information from amniotic fluid constituents.
Fuchs F
Clin Obstet Gynecol; 1966 Jun; 9(2):565-73. PubMed ID: 5330423
[No Abstract] [Full Text] [Related]
18. 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]
19. [Prenatal diagnosis of genetic diseases. Review of studies on amniotic fluid].
Guibaud P; Guibaud S
Lyon Med; 1970 Nov; 224(36):547-61. PubMed ID: 4926984
[No Abstract] [Full Text] [Related]
20. Prenatal detection of methylmalonic acidemia.
Marrow G; Schwarz RH; Hallock JA; Barness LA
J Pediatr; 1970 Jul; 77(1):120-3. PubMed ID: 5450273
[No Abstract] [Full Text] [Related]
[Next] [New Search]