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6. [Prenatal diagnosis of cutaneous genetic diseases by the study of fetal DNA]. Hovnanian A; De Prost Y Ann Dermatol Venereol; 1995; 122(4):173-85. PubMed ID: 8526412 [TBL] [Abstract][Full Text] [Related]
7. The spectrum of "complicated spastic paraplegia, MASA syndrome and X-linked hydrocephalus". Contribution of DNA linkage analysis in genetic counseling of individual families. Schrander-Stumpel C; Meyer H; Merckx D; Jones M; Israel J; Sommer A; Stevens C; Tinschert S; Wilson G; Willems P Genet Couns; 1994; 5(1):1-10. PubMed ID: 8031529 [TBL] [Abstract][Full Text] [Related]
8. [Possibilities and limitations of genetic family counseling (author's transl)]. Jörgensen G MMW Munch Med Wochenschr; 1981 Jul; 123(29-30):1167-72. PubMed ID: 6790955 [TBL] [Abstract][Full Text] [Related]
10. Ocular manifestations in female carriers of X-linked disorders. Nowakowski R J Am Optom Assoc; 1995 Jun; 66(6):352-6. PubMed ID: 7673594 [TBL] [Abstract][Full Text] [Related]
11. Familial hydrocephalus of prenatal onset. Zlotogora J; Sagi M; Cohen T Am J Med Genet; 1994 Jan; 49(2):202-4. PubMed ID: 8116668 [TBL] [Abstract][Full Text] [Related]
12. Association between HLA antigens and families with psoriasis vulgaris. Cao K; Song FJ; Li HG; Xu SY; Liu ZH; Su XH; Wang FX Chin Med J (Engl); 1993 Feb; 106(2):132-5. PubMed ID: 8504697 [TBL] [Abstract][Full Text] [Related]
13. A review of genetic mutation in familial Hirschsprung's disease in South Africa: towards genetic counseling. Moore SW; Zaahl MG J Pediatr Surg; 2008 Feb; 43(2):325-9. PubMed ID: 18280283 [TBL] [Abstract][Full Text] [Related]
14. [Genetic counseling, a contribution to family planning]. Theile U Fortschr Med; 1977 Mar; 95(10):620-6. PubMed ID: 66174 [TBL] [Abstract][Full Text] [Related]
15. [The selective effect of therapeutic abortion when children thus eliminated are carriers of a recessive autosomic or x-chromosome-linked defect]. Pfändler U; Kälin A J Genet Hum; 1972 Jun; 20(2):135-50. PubMed ID: 4660637 [No Abstract] [Full Text] [Related]
16. Genetic counselling in carriers of reciprocal chromosomal translocations involving short arm of chromosome X. Panasiuk B; Usinskiené R; Kostyk E; Rybałko A; Stasiewicz-Jarocka B; Krzykwa B; Pieńkowska-Grela B; Kucinskas V; Michalova K; Midro AT Ann Genet; 2004; 47(1):11-28. PubMed ID: 15050871 [TBL] [Abstract][Full Text] [Related]