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Items: 1 to 20 of 36

1.

The mutation rate of the gene for haemophilia, and its segregation ratios in males and females.

HALDANE JB.

Ann Eugen. 1947 Jun;13(4):262-71. No abstract available.

2.

Selection differentials and selection coefficients.

Milkman R.

Genetics. 1978 Feb;88(2):391-403.

3.

The mutational load with epistatic gene interactions in fitness.

Kimura M, Maruyama T.

Genetics. 1966 Dec;54(6):1337-51. No abstract available.

4.

Efficiency of truncation selection.

Crow JF, Kimura M.

Proc Natl Acad Sci U S A. 1979 Jan;76(1):396-9.

5.

Our load of mutations.

MULLER HJ.

Am J Hum Genet. 1950 Jun;2(2):111-76. No abstract available.

7.

Sex differences in mutation rate in higher primates estimated from AMG intron sequences.

Huang W, Chang BH, Gu X, Hewett-Emmett D, Li W.

J Mol Evol. 1997 Apr;44(4):463-5.

PMID:
9089087
8.

Prevalence and parental origin of de novo RET mutations in multiple endocrine neoplasia type 2A and familial medullary thyroid carcinoma. Le Groupe d'Etude des Tumeurs a Calcitonine.

Schuffenecker I, Ginet N, Goldgar D, Eng C, Chambe B, Boneu A, Houdent C, Pallo D, Schlumberger M, Thivolet C, Lenoir GM.

Am J Hum Genet. 1997 Jan;60(1):233-7. No abstract available.

9.

Nature of deleterious mutation load in Drosophila.

Keightley PD.

Genetics. 1996 Dec;144(4):1993-9.

10.

Sex differences in mutational rate and mutational mechanism in the NF1 gene in neurofibromatosis type 1 patients.

Lázaro C, Gaona A, Ainsworth P, Tenconi R, Vidaud D, Kruyer H, Ars E, Volpini V, Estivill X.

Hum Genet. 1996 Dec;98(6):696-9.

PMID:
8931703
11.

Human aneuploidy: incidence, origin, and etiology.

Hassold T, Abruzzo M, Adkins K, Griffin D, Merrill M, Millie E, Saker D, Shen J, Zaragoza M.

Environ Mol Mutagen. 1996;28(3):167-75. Review. No abstract available.

PMID:
8908177
12.

Comparing mutational variabilities.

Houle D, Morikawa B, Lynch M.

Genetics. 1996 Jul;143(3):1467-83. Review.

13.

A paternal wash in Apert syndrome.

Sapienza C.

Nat Genet. 1996 May;13(1):9-10. No abstract available.

PMID:
8673111
14.

Exclusive paternal origin of new mutations in Apert syndrome.

Moloney DM, Slaney SF, Oldridge M, Wall SA, Sahlin P, Stenman G, Wilkie AO.

Nat Genet. 1996 May;13(1):48-53.

PMID:
8673103
16.

Spontaneous mutation as a risk factor.

Crow JF.

Exp Clin Immunogenet. 1995;12(3):121-8. Review.

PMID:
8534499
17.

How much do we know about spontaneous human mutation rates?

Crow JF.

Environ Mol Mutagen. 1993;21(2):122-9. Erratum in: Environ Mol Mutagen 1993;21(4):389.

PMID:
8444142
18.

Trinucleotide repeat length instability and age of onset in Huntington's disease.

Duyao M, Ambrose C, Myers R, Novelletto A, Persichetti F, Frontali M, Folstein S, Ross C, Franz M, Abbott M, et al.

Nat Genet. 1993 Aug;4(4):387-92.

PMID:
8401587
19.
20.

Parent-of-origin effects in multiple endocrine neoplasia type 2B.

Carlson KM, Bracamontes J, Jackson CE, Clark R, Lacroix A, Wells SA Jr, Goodfellow PJ.

Am J Hum Genet. 1994 Dec;55(6):1076-82.

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