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4. Status and prospects of research in hereditary deafness. Nance WE; McConnell FE Adv Hum Genet; 1973; 4():173-250. PubMed ID: 4205901 [No Abstract] [Full Text] [Related]
5. Renal prognosis in Alport's and related syndromes: influence of the mode of inheritance. Pochet JM; Bobrie G; Landais P; Goldfarb B; Grünfeld JP Nephrol Dial Transplant; 1989; 4(12):1016-21. PubMed ID: 2517321 [TBL] [Abstract][Full Text] [Related]
7. "Counseling" in ophthalmology. Francois J Ann Ophthalmol; 1976 Mar; 8(3):265-75. PubMed ID: 1267307 [No Abstract] [Full Text] [Related]
8. [Sex-linked recessive hereditary deafness (author's transl)]. Lu SM Zhonghua Yi Xue Za Zhi; 1981 Nov; 61(11):666-7. PubMed ID: 6804044 [No Abstract] [Full Text] [Related]
9. Symposium on sensorineural hearing loss in children: early detection and intervention. Genetic factors in deafness of early life. Nance WE; Sweeney A Otolaryngol Clin North Am; 1975 Feb; 8(1):19-48. PubMed ID: 1090886 [TBL] [Abstract][Full Text] [Related]
10. "Genetic for medical practitioners". Ambani LM Q Med Rev; 1981 Oct; 32(4):1-43. PubMed ID: 7051087 [No Abstract] [Full Text] [Related]
11. Computers in paediatrics. 2. Genetic counselling for sex linked recessive conditions. Tay JS; Yip WC J Singapore Paediatr Soc; 1982; 24(3-4):125-32. PubMed ID: 6897846 [No Abstract] [Full Text] [Related]
13. [New aspects of carrier diagnosis and human genetic counseling in Duchenne and Becker muscular dystrophy]. Spiegler AW; Huppert P; Werner W; Metzke H; Strobel U; Köhler K; Gerhardt R; Kaufmann J; Herrmann FH Z Arztl Fortbild (Jena); 1988; 82(22):1139-42. PubMed ID: 3247797 [No Abstract] [Full Text] [Related]
14. Recurrence risks for near relatives of children with sensori-neural deafness. Koehn D; Morgan K; Fraser FC Genet Couns; 1990; 1(2):127-32. PubMed ID: 2080997 [TBL] [Abstract][Full Text] [Related]