Serveur d'exploration sur le lymphœdème - Curation (Ncbi)

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Asian Continental Ancestry Group < Asian Continental Ancestry Group (genetics) < Asian Continental Ancestry Group (statistics & numerical data)  Facettes :

List of bibliographic references

Number of relevant bibliographic references: 7.
Ident.Authors (with country if any)Title
000099 (1999) M A Kron [États-Unis] ; B. Ramirez ; V. Belizario ; J P PandeyImmunoglobulin allotypes among the Bicolanos of Sorsogon province, Luzon, Philippines: implications of phenotypes for filariasis.
000894 (2002) Tsutomu Ogata [Japon] ; Koji Muroya ; Goro Sasaki ; Gen Nishimura ; Hiroshi Kitoh ; Tadashi HattoriSHOX nullizygosity and haploinsufficiency in a Japanese family: implication for the development of Turner skeletal features.
002975 (2007) Zhengya Yu ; Jingjing Wang ; Shuling Peng ; Bing Dong ; Yang LiIdentification of a novel VEGFR-3 missense mutation in a Chinese family with hereditary lymphedema type I.
002B74 (2008) Takeshi Futatani [Japon] ; Eiji Nii ; Makoto Obata ; Fukiko Ichida ; Yoshie Okabe ; Hirokazu Kanegane ; Toshio MiyawakiMolecular characterization of two novel VEGFR3 mutations in Japanese families with Milroy's disease.
003C87 (2010) Ji-Qun Sheng [République populaire de Chine] ; Feng Zeng ; Chang Li ; Jing-Yu Liu ; Qing Wang ; Mu-Gen Liu[Identification of VEGFR3 gene mutation in a Chinese family with autosomal dominant primary congenital lymphoedema].
004295 (2011) Zulkarnain Md Idris [Malaisie] ; Noorizan Miswan ; Jamail Muhi ; Tajul Ariffin Awang Mohd ; Jürgen F J. Kun ; Rahmah NoordinAssociation of CTLA4 gene polymorphisms with lymphatic filariasis in an East Malaysian population.
007C79 (2015) N F Liu ; Z. Yu ; Y. Luo ; D. Sun ; Z. YanA NOVEL FLT4 GENE MUTATION AND MR LYMPHANGIOGRAPHY IN A CHINESE FAMILY WITH MILROY DISEASE.

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