Genomics < Genotype < Genotyping Techniques

Facettes : AffPays.f Mesh.f AffRegion.f AffVille.f

List of bibliographic references

Number of relevant bibliographic references: 45.
[0-20] [0 - 20][0 - 45][20-40]

Ident.	Authors (with country if any)	Title
000260 (1999)	A. Tsezou [Grèce] ; C. Hadjiathanasiou ; D. Gourgiotis ; A. Galla ; E. Kavazarakis ; A. Pasparaki ; M. Kapsetaki ; C. Sismani ; C. Theodoridis ; P C Patsalis ; N. Moschonas ; S. Kitsiou	Molecular genetics of Turner syndrome: correlation with clinical phenotype and response to growth hormone therapy.
000746 (2001)	E H Choi [États-Unis] ; P A Zimmerman ; C B Foster ; S. Zhu ; V. Kumaraswami ; T B Nutman ; S J Chanock	Genetic polymorphisms in molecules of innate immunity and susceptibility to infection with Wuchereria bancrofti in South India.
000754 (2001)	C. Boucher ; C. Sargent ; T. Ogata ; N. Affara	Breakpoint analysis of Turner patients with partial Xp deletions: implications for the lymphoedema gene location
000E72 (2003)	A. Evans ; R. Bell ; G. Brice ; P. Comeglio ; C. Lipede ; S. Jeffery ; Peter Mortimer (dermatologue)‎ [Royaume-Uni] ; M. Sarfarazi ; A. Child	Identification of eight novel VEGFR-3 mutations in families with primary congenital lymphoedema
001B14 (2004)	Valeria Brazzelli [Italie] ; Daniela Larizza ; Miriam Martinetti ; Sara Martinoli ; Valeria Calcaterra ; Annalisa De Silvestri ; Roberta Pandolfi ; Giovanni Borroni	Halo nevus, rather than vitiligo, is a typical dermatologic finding of turner's syndrome: clinical, genetic, and immunogenetic study in 72 patients.
001D35 (2005)	Melissa L. Loscalzo [États-Unis] ; Phillip L. Van ; Vincent B. Ho ; Vladimir K. Bakalov ; Douglas R. Rosing ; Carol A. Malone ; Harry C. Dietz ; Carolyn A. Bondy	Association between fetal lymphedema and congenital cardiovascular defects in Turner syndrome.
001D41 (2005)	M. Ng ; T. Andrew ; T. Spector ; S. Jeffery	Linkage to the FOXC2 region of chromosome 16 for varicose veins in otherwise healthy, unselected sibling pairs
001E38 (2005)	Seiji Mizuno [Japon] ; Yasukazu Yamada ; Kenichiro Yamada ; Noriko Nomura ; Nobuaki Wakamatsu	Clinical variability in a Japanese hereditary lymphedema type I family with an FLT4 mutation.
002083 (2005)	K S Joiner [États-Unis] ; S J Ewald ; F J Hoerr ; V L Van Santen ; H. Toro	Oral infection with chicken anemia virus in 4-wk broiler breeders: lack of effect of major histocompatibility B complex genotype.
002552 (2007)	K P Patra [Inde] ; Thangadurai Ramu ; S L Hoti ; G Siva Pragasam ; P K Das	Identification of a molecular marker for genotyping human lymphatic filarial nematode parasite Wuchereria bancrofti.
002572 (2007)	Mylène Béri-Deixheimer [France] ; Marie-José Gregoire ; Annick Toutain ; Karène Brochet ; Sylvain Briault ; Jean-Luc Schaff ; Bruno Leheup ; Philippe Jonveaux	Genotype-phenotype correlations to aid in the prognosis of individuals with uncommon 20q13.33 subtelomere deletions: a collaborative study on behalf of the 'association des Cytogénéticiens de langue Française'.
002773 (2007)	Michael T. Dellinger [États-Unis] ; Robert J. Hunter ; Michael J. Bernas ; Marlys H. Witte ; Robert P. Erickson	Chy-3 mice are Vegfc haploinsufficient and exhibit defective dermal superficial to deep lymphatic transition and dermal lymphatic hypoplasia.
002975 (2007)	Zhengya Yu ; Jingjing Wang ; Shuling Peng ; Bing Dong ; Yang Li	Identification of a novel VEGFR-3 missense mutation in a Chinese family with hereditary lymphedema type I.
002B19 (2008)	Sajid Malik [Allemagne] ; Karl-Heinz Grzeschik	Congenital, low penetrance lymphedema of lower limbs maps to chromosome 6q16.2-q22.1 in an inbred Pakistani family.
002F27 (2008)	S L Hoti [Inde] ; Rohit Sharma ; K Athisaya Mary ; R. Dhamodharan ; K. Krishnamoorthy ; P K Das	A method for detecting microfilaraemia, filarial specific antigens and antibodies and typing of parasites for drug resistance and genotypes using finger prick blood sample.
003128 (2008)	Rui-Cheng Ji [Japon]	Lymphatic endothelial cells, lymphedematous lymphangiogenesis, and molecular control of edema formation.
003727 (2010)	Fiona Connell [Royaume-Uni] ; Kamini Kalidas ; Pia Ostergaard ; Glen Brice ; Tessa Homfray ; Lesley Roberts ; David J. Bunyan ; Sally Mitton ; Sahar Mansour ; Peter Mortimer (dermatologue)‎ [Royaume-Uni] ; Steve Jeffery	Linkage and sequence analysis indicate that CCBE1 is mutated in recessively inherited generalised lymphatic dysplasia.
003835 (2010)	E Henrike Mittmann [Allemagne] ; Stefanie Mömke ; Ottmar Distl	Whole-genome scan identifies quantitative trait loci for chronic pastern dermatitis in German draft horses.
003B82 (????)	Sophia Kitsiou-Tzeli [Grèce] ; Christina Vrettou ; Eleni Leze ; Periklis Makrythanasis ; Emmanouel Kanavakis ; Patrick Willems	Milroy's primary congenital lymphedema in a male infant and review of the literature.
004295 (2011)	Zulkarnain Md Idris [Malaisie] ; Noorizan Miswan ; Jamail Muhi ; Tajul Ariffin Awang Mohd ; Jürgen F J. Kun ; Rahmah Noordin	Association of CTLA4 gene polymorphisms with lymphatic filariasis in an East Malaysian population.
004604 (2011)	Alexander Yaw Debrah [Ghana] ; Linda Batsa ; Anna Albers ; Sabine Mand ; Mohammad Reza Toliat ; Peter Nürnberg ; Ohene Adjei ; Achim Hoerauf ; Kenneth Pfarr	Transforming growth factor-β1 variant Leu10Pro is associated with both lack of microfilariae and differential microfilarial loads in the blood of persons infected with lymphatic filariasis.

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