نتائج البحث

Variation in mutation rate and direction between tetranucleotide STR loci in human colorectal carcinomas

• Authors : Gunn Iren Meling; P. Hoff-Olsen; Bjørnar Olaisen

Subjects: Genetics; medicine.medical_specialty; Mutation rate

• Source: Annals of human genetics. 62(Pt 1)

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GJB2-related hearing loss in central Iran: Review of the spectrum and frequency of gene mutations.

• Authors : Koohiyan M; Cancer Research Center, Shahrekord University of Medical Sciences, Shahrekord, Iran.; Koohian F

Subjects: Mutation*; Connexins/Connexins/Connexins/*genetics ; Hearing Loss/Hearing Loss/Hearing Loss/*genetics

• Source: Annals of human genetics [Ann Hum Genet] 2020 Mar; Vol. 84 (2), pp. 107-113. Date of Electronic Publication: 2019 Sep 11.Publisher: Wiley-Blackwell Country of Publication: England NLM ID: 0416661 Publication Model: Print-Electronic Cited Medium: Internet ISSN:

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Variation in the VWF Gene in Swedish Patients with Type 1 von Willebrand Disease

• Authors : Anna Johansson; Christer Halldén; Stefan Lethagen

Subjects: Genetics; Nonsynonymous substitution; education.field_of_study

• Source: Annals of Human Genetics. 75:447-455

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Mutation spectrum of the fibrillin-1 (FBN1) gene in Taiwanese patients with Marfan syndrome

• Authors : Dau Ming Niu; Yi Ning Su; Shuan-Pei Lin

Subjects: musculoskeletal diseases; congenital, hereditary, and neonatal diseases and abnormalities; Mutation rate

• Source: Annals of Human Genetics. 73:559-567

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Haplotype analysis of the human alpha2-HS glycoprotein (fetuin) gene

• Authors : T. Udono; Naruya Saitou; Takashi Kitano

Subjects: Nonsynonymous substitution; Mutation rate; Pan troglodytes

• Source: Annals of Human Genetics. 65:27-34

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Maternal and paternal lineages of the Samaritan isolate: mutation rates and time to most recent common male ancestor

• Authors : Matthew E. Kaplan; Michael F. Hammer; Batsheva Bonne-Tamir

Subjects: Most recent common ancestor; Male; Mitochondrial DNA

• Source: Annals of human genetics. 67(Pt 2)

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RISCALW: a Windows program for risk calculation in families with Duchenne muscular dystrophy

• Authors : W. Gross; Christine Fischer; J. Krüger

Subjects: Genetics; Genetic Markers; Risk

• Source: Annals of human genetics. 70(Pt 2)

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The frequency in Japanese of genetic variants of 22 proteins I. Albumin, Ceruloplasmin, Haptoglobin, and Transferrin

• Authors : Chiyoko Satoh; T. Inamizu; Howard B. Hamilton

Subjects: Genetics; chemistry.chemical_classification; Mutation rate

• Source: Annals of Human Genetics. 40:407-418

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The frequency in Japanese of genetic variants of 22 proteins: V. Summary and comparison with data on Caucasians from the British Isles

• Authors : Chiyoko Satoh; N. Ueda; H. B. Hamilton

Subjects: Adult; Male; Genetics

• Source: Annals of Human Genetics. 41:429-441

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Familial Mediterranean Fever In Lebanon: Founder Effects For Different MEFV Mutations.

• Authors : Jalkh, Nadine¹; Génin, Emmanuelle^2,3; Chouery, Eliane^1,4

• Source: Annals of Human Genetics. Jan2008, Vol. 72 Issue 1, p41-47. 7p. 3 Charts, 1 Graph.

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