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Are children of older fathers at risk for genetic disorders?

Are children of older fathers at risk for genetic disorders?

http://www.wikidata.org/entity/Q47652949

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Association of paternal age at birth and the risk of breast cancer in offspring: a case control study Statement on guidance for genetic counseling in advanced paternal age The participation of prospective fathers in preconception care Advanced paternal age and mortality of offspring under 5 years of age: a register-based cohort study.Could autism with mental retardation result from digenism and frequent de novo mutations?Ionizing radiation-induced mutant frequencies increase transiently in male germ cells of older mice.Early life factors and adult mammographic density.Sperm concentration and normal sperm morphology decrease and follicle-stimulating hormone level increases with age.Characteristics, causes and evolutionary consequences of male-biased mutation.Parental age and risk of genetic syndromes predisposing to nervous system tumors: nested case-control study.The Concept of Schizophrenia: From Unity to Diversity Schizophrenia: The Epidemiological Horizon

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Are children of older fathers at risk for genetic disorders?

http://www.wikidata.org/entity/Q47652949

description

2003 nî lūn-bûn

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2003年の論文

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2003年学术文章

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2003年学术文章

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2003年学术文章

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2003年学术文章

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2003年学术文章

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2003年學術文章

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2003年學術文章

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Are children of older fathers at risk for genetic disorders?

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Are children of older fathers at risk for genetic disorders?

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Are children of older fathers at risk for genetic disorders?

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Are children of older fathers at risk for genetic disorders?

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Are children of older fathers at risk for genetic disorders?

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Are children of older fathers at risk for genetic disorders?

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J.1439-0272.2003.00579.X

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Are children of older fathers at risk for genetic disorders?

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Jung A

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Schill WB

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Schuppe HC

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P2860

MECP2 mutations in sporadic cases of Rett syndrome are almost exclusively of paternal origin

The high spontaneous mutation rate: is it a health risk?

Paternal age and sporadic schizophrenia: evidence for de novo mutations

Clinical and molecular characterisation of 80 patients with 5p deletion: genotype-phenotype correlation

Paternal origin of FGFR2 mutations in sporadic cases of Crouzon syndrome and Pfeiffer syndrome

The origins, patterns and implications of human spontaneous mutation

Male-driven evolution of DNA sequences

Long-term effects of delayed parenthood

Clinical spectrum of fibroblast growth factor receptor mutations.

Nondisjunction in trisomy 21: origin and mechanisms.

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191-199

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scholarly article

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10.1046/J.1439-0272.2003.00579.X

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4

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35

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2003-08-01T00:00:00Z

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