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22. Prenatal diagnosis for a novel homozygous mutation in PKLR gene in an Indian family. Gupta N; Bianchi P; Fermo E; Kabra M; Warang P; Kedar P; Gupta N; Colah R Prenat Diagn; 2007 Feb; 27(2):117-8. PubMed ID: 17191259 [TBL] [Abstract][Full Text] [Related]
23. Basic concepts in biochemical antenatal diagnosis. Grebner EE Obstet Gynecol Clin North Am; 1993 Sep; 20(3):421-31. PubMed ID: 8278142 [TBL] [Abstract][Full Text] [Related]
24. [Fucosidosis: review of personal experience]. Filocamo M; Di Rocco M; Rolando S; Schiappapietra M; Costantino G Pediatr Med Chir; 1982; 4(3):185-94. PubMed ID: 7170189 [TBL] [Abstract][Full Text] [Related]
25. Prenatal diagnosis of carbamoyl phosphate synthetase I deficiency by identification of a missense mutation in CPS1. Finckh U; Kohlschütter A; Schäfer H; Sperhake K; Colombo JP; Gal A Hum Mutat; 1998; 12(3):206-11. PubMed ID: 9711878 [TBL] [Abstract][Full Text] [Related]
26. [Prenatal diagnosis: a new problem]. Cutillo S Pediatria (Napoli); 1980 Jun; 88(2):V-VII. PubMed ID: 7243515 [No Abstract] [Full Text] [Related]
27. [Prenatal diagnosis: results and risks experienced in West Germany]. Stengel-Rutkowski S J Genet Hum; 1980 Jun; 28(2):73-88. PubMed ID: 7463012 [No Abstract] [Full Text] [Related]
28. [Molecular biology diagnostics of hereditary metabolic diseases]. Christensen B; Berg K Tidsskr Nor Laegeforen; 1998 Apr; 118(11):1737-42. PubMed ID: 9621764 [TBL] [Abstract][Full Text] [Related]
33. Prenatal molecular diagnosis of glutaric aciduria type I by direct mutation analysis. Busquets C; Coll MJ; Merinero B; Ugarte M; Ruiz MA; Martinez Bermejo A; Ribes A Prenat Diagn; 2000 Sep; 20(9):761-4. PubMed ID: 11015709 [TBL] [Abstract][Full Text] [Related]
34. The invasive prenatal diagnosis in perinatal centre. Hájek Z; Koleska T; Drbohlav P; Spálová I; Macek M; Stejskal D; Kvasnicka J Sb Lek; 1997; 98(2):99-105. PubMed ID: 9601802 [TBL] [Abstract][Full Text] [Related]
35. [Possibilities for diminution of the genetic risk in the population]. Knapp A; Machill G Z Arztl Fortbild (Jena); 1976 Aug; 69(16):845-51. PubMed ID: 1244694 [No Abstract] [Full Text] [Related]
36. Avoiding serious birth defects by prenatal diagnosis: current effect on birth incidence. Ferguson-Smith MA Proc Annu Symp Eugen Soc; 1981; 16():121-33. PubMed ID: 7050971 [No Abstract] [Full Text] [Related]
37. [Interruption of pregnancy based on prenatal diagnosis]. Murken JD; Stengel-Rutkowski S; Wirtz A Hautarzt; 1980; 31 Suppl 4():25-30. PubMed ID: 7399930 [TBL] [Abstract][Full Text] [Related]
38. [Modern possibilities in the early diagnosis of congenital metabolic diseases]. Schreier K Med Welt; 1982 Apr; 33(13):462-5. PubMed ID: 7087722 [No Abstract] [Full Text] [Related]
39. Prenatal diagnosis of some metabolic diseases using early amniotic fluid samples: report of a 15 years, experience. Chadefaux-Vekemans B; Rabier D; Cadoudal N; Lescoat A; Chabli A; Aupetit J; Dumez Y; Oury JF Prenat Diagn; 2006 Sep; 26(9):814-8. PubMed ID: 16821251 [TBL] [Abstract][Full Text] [Related]