211 related articles for article (PubMed ID: 6496641)
1. Bayes' theorem and X-linked ophthalmic disorders.
Nowakowski RW
Am J Optom Physiol Opt; 1984 Oct; 61(10):643-6. PubMed ID: 6496641
[TBL] [Abstract][Full Text] [Related]
2. 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]
3. 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]
4. Genetic counseling in Becker type X-linked muscular dystrophy. I. Theoretical considerations.
Grimm T
Am J Med Genet; 1984 Aug; 18(4):713-8. PubMed ID: 6486169
[TBL] [Abstract][Full Text] [Related]
5. Issues in the application of Bayes' Theorem to child abuse decision making.
Proeve M
Child Maltreat; 2009 Feb; 14(1):114-20. PubMed ID: 18495947
[TBL] [Abstract][Full Text] [Related]
6. [The use of Bayes theorum in genetic counseling in cases of Duchenne muscular dystrophy].
Dodinval P
J Genet Hum; 1979 Jun; 27(2):131-43. PubMed ID: 541678
[TBL] [Abstract][Full Text] [Related]
7. Useful probability considerations in genetics: the goat problem with tigers and other applications of Bayes' theorem.
Oexle K
Eur J Pediatr; 2006 May; 165(5):299-305. PubMed ID: 16463135
[TBL] [Abstract][Full Text] [Related]
8. [Congenital dyschromatopsia. I. Genetic aspects].
Klein D
J Genet Hum; 1986 Jan; 34(1):75-86. PubMed ID: 3485700
[No Abstract] [Full Text] [Related]
9. 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]
10. [Genetic prognosis in ophthalmology].
François J
Annee Ther Clin Ophtalmol; 1972; 23():319-30. PubMed ID: 4680285
[No Abstract] [Full Text] [Related]
11. A counseling guide to the Martin-Bell syndrome.
Weaver DD; Sherman SL
Am J Med Genet; 1987 Jan; 26(1):39-44. PubMed ID: 3812576
[No Abstract] [Full Text] [Related]
12. Bayes' theorem--a review.
Schulman P
Cardiol Clin; 1984 Aug; 2(3):319-28. PubMed ID: 6399868
[TBL] [Abstract][Full Text] [Related]
13. Significance of phenotypic and chromosomal abnormalities in X-linked mental retardation (Martin-Bell or Renpenning syndrome).
Jennings M; Hall JG; Hoehn H
Am J Med Genet; 1980; 7(4):417-32. PubMed ID: 6938131
[TBL] [Abstract][Full Text] [Related]
14. Osteopathia striata with cranial sclerosis: literature reappraisal argues for X-linked inheritance.
Behninger C; Rott HD
Genet Couns; 2000; 11(2):157-67. PubMed ID: 10893667
[TBL] [Abstract][Full Text] [Related]
15. Multiple simultaneous predictors of gestational age. An application of Bayes' theorem.
Rose BI; Lamb EJ
Am J Perinatol; 1988 Jan; 5(1):44-50. PubMed ID: 3276338
[TBL] [Abstract][Full Text] [Related]
16. [X-chromosomal hereditary night blindness: detection of carriers by segregation analysis with linked DNA markers].
Orth U; Schinzel A; Mächler M; Gal A
Klin Monbl Augenheilkd; 1990 May; 196(5):269-72. PubMed ID: 2366451
[TBL] [Abstract][Full Text] [Related]
17. [Genetic counseling for dermatologic patients].
Walther JU
Hautarzt; 1982 Feb; 33(2):54-61. PubMed ID: 7076499
[TBL] [Abstract][Full Text] [Related]
18. Enter the reverend: introduction to and application of Bayes' theorem in clinical ophthalmology.
Thomas R; Mengersen K; Parikh RS; Walland MJ; Muliyil J
Clin Exp Ophthalmol; 2011 Dec; 39(9):865-70. PubMed ID: 21575118
[TBL] [Abstract][Full Text] [Related]
19. [X chronmosome-linked hydrocephalus. Diagnostic and genetic-counseling aspects].
Kocoń-Sladowska H; Sito A; Maślińska D
Pediatr Pol; 1980 Apr; 55(4):463-71. PubMed ID: 7191083
[No Abstract] [Full Text] [Related]
20. X-linked mental retardation with heterozygous expression and macrocephaly: pericentromeric gene localization.
Turner G; Gedeon A; Mulley J
Am J Med Genet; 1994 Jul; 51(4):575-80. PubMed ID: 7943042
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]