MeSH Review:
Paternal Age
Tartaglia,
Cordeddu,
Chang,
Shaw,
Kalidas,
Crosby,
Patton,
Sorcini,
van der Burgt,
Jeffery,
Gelb,
Montgomery,
Lambe,
Olsson,
Ekbom,
Bunin,
Needle,
Riccardi,
Shotelersuk,
Mahatumarat,
Ittiwut,
Rojvachiranonda,
Srivuthana,
Wacharasindhu,
Tongkobpetch,
Wilkin,
Szabo,
Cameron,
Henderson,
Bellus,
Mack,
Kaitila,
Loughlin,
Munnich,
Sykes,
Bonaventure,
Francomano,
Wuyts,
Biervliet,
Reyniers,
D'Apice,
Novelli,
Storm,
- Mutations in fibroblast growth-factor receptor 3 in sporadic cases of achondroplasia occur exclusively on the paternally derived chromosome. Wilkin, D.J., Szabo, J.K., Cameron, R., Henderson, S., Bellus, G.A., Mack, M.L., Kaitila, I., Loughlin, J., Munnich, A., Sykes, B., Bonaventure, J., Francomano, C.A. Am. J. Hum. Genet. (1998)
- Paternal germline origin and sex-ratio distortion in transmission of PTPN11 mutations in Noonan syndrome. Tartaglia, M., Cordeddu, V., Chang, H., Shaw, A., Kalidas, K., Crosby, A., Patton, M.A., Sorcini, M., van der Burgt, I., Jeffery, S., Gelb, B.D. Am. J. Hum. Genet. (2004)
- Inverse relationship between age at onset of Huntington disease and paternal age suggests involvement of genetic imprinting. Farrer, L.A., Cupples, L.A., Kiely, D.K., Conneally, P.M., Myers, R.H. Am. J. Hum. Genet. (1992)
- Predictors of IDDM recurrence risk in offspring of Danish IDDM patients. Danish IDDM Epidemiology and Genetics Group. Lorenzen, T., Pociot, F., Stilgren, L., Kristiansen, O.P., Johannesen, J., Olsen, P.B., Walmar, A., Larsen, A., Albrechtsen, N.C., Eskildsen, P.C., Andersen, O.O., Nerup, J. Diabetologia (1998)
- Paternal age effect in fibrodysplasia ossificans progressiva. Rogers, J.G., Chase, G.A. J. Med. Genet. (1979)
- A genetic study of torsion dystonia. Bundey, S., Harrison, M.J., Marsden, C.D. J. Med. Genet. (1975)
- The relation of birth rank and parental age to the phenotype distributions of 14 genetic systems in an Australian population sample. Brackenridge, C.J., Case, J., Sheehy, A.J. Hum. Hered. (1976)
- Variation in prenatal cytogenetic diagnosis: policies in 13 European countries, 1989-1991. EUROCAT Working Group. European Registration of Congenital Anomalies. Cornel, M.C. Prenat. Diagn. (1994)
- FGFR2 mutations among Thai children with Crouzon and Apert syndromes. Shotelersuk, V., Mahatumarat, C., Ittiwut, C., Rojvachiranonda, N., Srivuthana, S., Wacharasindhu, S., Tongkobpetch, S. The Journal of craniofacial surgery. (2003)
- Somatic and gonadal mosaicism in Hutchinson-Gilford progeria. Wuyts, W., Biervliet, M., Reyniers, E., D'Apice, M.R., Novelli, G., Storm, K. Am. J. Med. Genet. A (2005)
- Epidemiology of presenile Alzheimer's disease in Scotland (1974-88) II. Exposures to possible risk factors. Whalley, L.J., Thomas, B.M., Starr, J.M. The British journal of psychiatry : the journal of mental science. (1995)
- Clinical and genetic heterogeneity in retinitis pigmentosa. Kaplan, J., Bonneau, D., Frézal, J., Munnich, A., Dufier, J.L. Hum. Genet. (1990)
- Parental age, family size, and risk of multiple sclerosis. Montgomery, S.M., Lambe, M., Olsson, T., Ekbom, A. Epidemiology (Cambridge, Mass.) (2004)
- Paternal age and sporadic neurofibromatosis 1: a case-control study and consideration of the methodologic issues. Bunin, G.R., Needle, M., Riccardi, V.M. Genet. Epidemiol. (1997)