Titlebook: Werner’s Syndrome and Human Aging; Darrell Salk,Yoshisada Fujiwara,George M. Martin Book 1985 The Editor(s) (if applicable) and The Author

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書目名稱Werner’s Syndrome and Human Aging影響因子(影響力)




書目名稱Werner’s Syndrome and Human Aging影響因子(影響力)學科排名




書目名稱Werner’s Syndrome and Human Aging網(wǎng)絡(luò)公開度




書目名稱Werner’s Syndrome and Human Aging網(wǎng)絡(luò)公開度學科排名




書目名稱Werner’s Syndrome and Human Aging被引頻次




書目名稱Werner’s Syndrome and Human Aging被引頻次學科排名




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書目名稱Werner’s Syndrome and Human Aging年度引用學科排名




書目名稱Werner’s Syndrome and Human Aging讀者反饋




書目名稱Werner’s Syndrome and Human Aging讀者反饋學科排名

和諧

Werner’s Syndrome: A Review of its Symptomatology, Natural History, Pathologic Features, Genetics anination with scleroderma”) (137). He reported four sibs with similar clinical findings: shortness of stature; senile appearance; graying of the hair beginning at about age 20; cataracts appearing during the third decade; skin changes (tautness, atrophy, hyperkeratoses and ulceration) designated as s

Arresting

顧客

Keynote Address: Genetics and Aging; The Werner Syndrome as a Segmental Progeroid Syndromepment and in the domain of the maintenance of macromolecular integrity. The enormous genetic hererogeneity that characterizes our own species, the complexities of numerous nature-nurture interactions, and the quantitative and qualitative variations of the senescent phenotype that are observed sugges

Exonerate

placebo-effect

finite

獸皮

Werner’s Syndrome and Aging: A Reappraisalature indicate either an ambivalence about this relationship or a belief that the two conditions are fundamentally related to one another. Therefore, the criteria for premature aging originally used have been reexamined and found to be still acceptable. Evaluation of the features of the Werner syndr

繁殖

A Comparison of Adult and Childhood Progerias: Werner Syndrome and Hutchinson-Gilford Progeria Syndrenetic disease models of human aging (Brown, 1979). A comparison of their similarities and differences may be useful in order to gain insight into the nature of the genetic mutations underlying these conditions. Their modes of inheritance indicate the involvement of a single gene. This implies that

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