These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.
2. Introduction of genomic diagnosis of classical phenylketonuria to the health care system of the German Democratic Republic. Riess O; Michel A; Speer A; Cobet G; Coutelle C Clin Genet; 1987 Oct; 32(4):209-15. PubMed ID: 2890455 [TBL] [Abstract][Full Text] [Related]
3. Prenatal diagnosis of classical phenylketonuria by linked restriction fragment length polymorphism analysis. Speer A; Bollman R; Michel A; Neumann R; Bommer C; Hanke R; Riess O; Cobet G; Coutelle C Prenat Diagn; 1986; 6(6):447-50. PubMed ID: 2880342 [TBL] [Abstract][Full Text] [Related]
4. [Prenatal diagnosis of phenylketonuria (with a report of 10 cases)]. Zeng YT Zhonghua Yi Xue Za Zhi; 1988 Feb; 68(2):61-4. PubMed ID: 2900675 [No Abstract] [Full Text] [Related]
5. Application of a new DNA sequence polymorphism as a genetic marker in prenatal diagnosis of phenylketonuria. Huang SZ; Ren ZR; Zeng YT J Med Genet; 1990 Jan; 27(1):65-6. PubMed ID: 1968515 [No Abstract] [Full Text] [Related]
6. [Genetic diagnosis in classical phenylketonuria]. Wulff K; Herrmann FH; Wehnert M; Seidlitz G; Schütz M Z Arztl Fortbild (Jena); 1988; 82(22):1127-31. PubMed ID: 2907835 [No Abstract] [Full Text] [Related]
7. Progress in the identification of the heterozygote in phenylketonuria. Lehmann WD J Pediatr; 1989 Jun; 114(6):915-24. PubMed ID: 2566668 [No Abstract] [Full Text] [Related]
8. Prenatal diagnosis of phenylketonuria. Kohli S; Saxena R; Thomas E; Rao P; Verma IC Indian J Med Res; 2005 Nov; 122(5):400-3. PubMed ID: 16456253 [TBL] [Abstract][Full Text] [Related]
9. Molecular genetic analysis of phenylketonuria and mental retardation. Woo SL Res Publ Assoc Res Nerv Ment Dis; 1991; 69():193-203. PubMed ID: 1672237 [No Abstract] [Full Text] [Related]
11. [Genetic heterogeneity and approaches to the prenatal diagnosis of phenylketonuria (review)]. Chestkov VV; Shishkin SS Vopr Med Khim; 1986; 32(4):7-12. PubMed ID: 3020793 [TBL] [Abstract][Full Text] [Related]
12. Molecular studies and prenatal diagnosis of phenylketonuria in Chinese patients. Fan GX; Qing LX; Jun Y; Mei Z Southeast Asian J Trop Med Public Health; 1999; 30 Suppl 2():63-5. PubMed ID: 11400788 [TBL] [Abstract][Full Text] [Related]
17. Maternal phenylketonuria: finding and treating women before conception. Hanley WB; Bell L Can Med Assoc J; 1982 Jun; 126(11):1259-60. PubMed ID: 7074445 [No Abstract] [Full Text] [Related]
19. [Mutation analysis of phenylalanine hydroxylase gene in patients w ith phenylketonuria in Henan province]. GUO HJ; ZHAO ZH; JIANG M; SHI HR; KONG XD Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2011 Apr; 28(2):142-6. PubMed ID: 21462123 [TBL] [Abstract][Full Text] [Related]
20. [Prenatal screening for phenylketonuria in 2 families by trophoblast biopsy]. Rey F; Berthelon M; Munnich A; Frézal J; Rey J Arch Fr Pediatr; 1987 Oct; 44(8):565-8. PubMed ID: 2894821 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]