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8. [The practicing physician facing current problems in genetics]. Juillard E; Grosset L Rev Med Suisse Romande; 1973 Sep; 93(9):655-68. PubMed ID: 4272167 [No Abstract] [Full Text] [Related]
9. [Cytogenetic studies in clinical diagnosis --analysis of 1611 examination results]. Bocian E; Mazurczak T; Stańczak H Przegl Lek; 1995; 52(1):5-9. PubMed ID: 7784612 [TBL] [Abstract][Full Text] [Related]
10. Prader--Willi syndrome associated with an interstitial deletion of chromosome 15. Bonuccelli CM; Stetten G; Levitt RC; Levin LS; Pyeritz RE Johns Hopkins Med J; 1982 Nov; 151(5):237-42. PubMed ID: 7143875 [No Abstract] [Full Text] [Related]
11. [Prenatal chromosome analysis in risk fetuses]. Philip J; Bang J; Hahnemann N; Mikkelsen M; Niebuhr E; Rebbe H; Weber J Ugeskr Laeger; 1974 Jul; 136(29):1621-4. PubMed ID: 4276782 [No Abstract] [Full Text] [Related]
12. Prenatal diagnosis of Prader-Willi syndrome using PW71 methylation analysis--uniparental disomy and the significance of residual trisomy 15. Slater HR; Vaux C; Pertile M; Burgess T; Petrovic V Prenat Diagn; 1997 Feb; 17(2):109-13. PubMed ID: 9061757 [TBL] [Abstract][Full Text] [Related]
13. Prenatal diagnosis of uniparental disomy 15 following trisomy 15 mosaicism. Christian SL; Smith AC; Macha M; Black SH; Elder FF; Johnson JM; Resta RG; Surti U; Suslak L; Verp MS; Ledbetter DH Prenat Diagn; 1996 Apr; 16(4):323-32. PubMed ID: 8734806 [TBL] [Abstract][Full Text] [Related]
14. Age-specific incidences of chromosome abnormalities at the second trimester amniocentesis for Japanese mothers aged 35 and older: collaborative study of 5484 cases. Yaegashi N; Senoo M; Uehara S; Suzuki H; Maeda T; Fujimori K; Hirahara F; Yajima A J Hum Genet; 1998; 43(2):85-90. PubMed ID: 9621511 [TBL] [Abstract][Full Text] [Related]
15. [Prenatal sex determination and cytogenetics]. Zellweger H; White CA; Kretzschmar RM Schweiz Med Wochenschr; 1971 Oct; 101(41):1464-70. PubMed ID: 4259054 [No Abstract] [Full Text] [Related]
16. [Prenatal chromosome analysis using the FISH technique allows fetal aneuploidy detection within a few hours]. Steinborn A; Röddiger S; Born HJ; Baier P; Halberstadt E Z Geburtshilfe Neonatol; 1996; 200(5):186-90. PubMed ID: 9035828 [TBL] [Abstract][Full Text] [Related]
17. [Indications for chromosome analysis]. Pfeiffer RA Fortschr Med; 1985 Jan; 103(3):33-6. PubMed ID: 3156080 [No Abstract] [Full Text] [Related]
18. The cytogenetic controversy in the Prader-Labhart-Willi syndrome. Kousseff BG Am J Med Genet; 1982 Dec; 13(4):431-9. PubMed ID: 7158643 [TBL] [Abstract][Full Text] [Related]