Human Genetics,volume 115,issue 1  (06-2004)

Period of time: 2004年1期

Publisher: Springer Publishing Company

Founded in: 1913

Total resources: 46

ISSN: 0340-6717

Subject: Q3 Genetics

Favorite

Disclaimer: Any content in publications that violate the sovereignty, the constitution or regulations of the PRC is not accepted or approved by CNPIEC.

Human Genetics,volume 115,issue 1

Menu

Small marker chromosomes in two patients with segmental aneusomy for proximal 17p

By Shaw Christine,Stankiewicz Pawel,Bien-Willner Gabriel,Bello Scott,Shaw Chad,Carrera Marta,Perez Jurado Luis,Estivill Xavier,Lupski James in (2004)

Human Genetics,volume 115,issue 1 , Vol. 115, Iss. 1, 2004-06 , pp. 1-7

Springer Publishing Company

Abstract Access to resources Recommend Favorite

Lipoprotein lipase gene is in linkage with blood pressure phenotypes in Chinese pedigrees

By Yang Wenjie,Huang Jianfeng,Ge Dongliang,Yao Cailiang,Duan Xiufang,Shen Yan,Qiang Boqin,Gu Dongfeng in (2004)

Human Genetics,volume 115,issue 1 , Vol. 115, Iss. 1, 2004-06 , pp. 8-12

Springer Publishing Company

Abstract Access to resources Recommend Favorite

An intragenic deletion/inversion event in the DMD gene determines a novel exon creation and results in a BMD phenotype

By Cagliani Rachele,Sironi Manuela,Ciafaloni Emma,Bardoni Alessandra,Fortunato Francesco,Prelle Alessandro,Serafini Massimo,Bresolin Nereo,Comi Giacomo in (2004)

Human Genetics,volume 115,issue 1 , Vol. 115, Iss. 1, 2004-06 , pp. 13-18

Springer Publishing Company

Abstract Access to resources Recommend Favorite

The origin of the isolated population of the Faroe Islands investigated using Y chromosomal markers

By Jorgensen Tove,Buttenschön Henriette,Wang August,Als Thomas,Børglum Anders,Ewald Henrik in (2004)

Human Genetics,volume 115,issue 1 , Vol. 115, Iss. 1, 2004-06 , pp. 19-28

Springer Publishing Company

Abstract Access to resources Recommend Favorite

Mitochondrial DNA polymorphisms as risk factors for Parkinson’s disease and Parkinson’s disease dementia

By Autere Jaana,Moilanen Jukka,Finnilä Saara,Soininen Hilkka,Mannermaa Arto,Hartikainen Päivi,Hallikainen Merja,Majamaa Kari in (2004)

Human Genetics,volume 115,issue 1 , Vol. 115, Iss. 1, 2004-06 , pp. 29-35

Springer Publishing Company

Abstract Access to resources Recommend Favorite

The effects of scale: variation in the APOA1/C3/A4/A5 gene cluster

By Fullerton Stephanie,Buchanan Anne,Sonpar Vibhor,Taylor Scott,Smith Joshua,Carlson Christopher,Salomaa Veikko,Stengård Jari,Boerwinkle Eric,Clark Andrew,Nickerson Deborah,Weiss Kenneth in (2004)

Human Genetics,volume 115,issue 1 , Vol. 115, Iss. 1, 2004-06 , pp. 36-56

Springer Publishing Company

Abstract Access to resources Recommend Favorite

Evidence for non-homologous end joining and non-allelic homologous recombination in atypical NF1 microdeletions

By Venturin Marco,Gervasini Cristina,Orzan Francesca,Bentivegna Angela,Corrado Lucia,Colapietro Patrizia,Friso Alessandra,Tenconi Romano,Upadhyaya Meena,Larizza Lidia,Riva Paola in (2004)

Human Genetics,volume 115,issue 1 , Vol. 115, Iss. 1, 2004-06 , pp. 69-80

Springer Publishing Company

Abstract Access to resources Recommend Favorite

SNTG1, the gene encoding γ1-syntrophin: a candidate gene for idiopathic scoliosis

By Bashiardes Stavros,Veile Rose,Allen Missy,Wise Carol,Dobbs Mathew,Morcuende Jose,Szappanos Lazlos,Herring John,Bowcock Anne,Lovett Michael in (2004)

Human Genetics,volume 115,issue 1 , Vol. 115, Iss. 1, 2004-06 , pp. 81-89

Springer Publishing Company

Abstract Access to resources Recommend Favorite