Genetic Heterogeneity < Genetic Linkage < Genetic Linkage (genetics)

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List of bibliographic references indexed by Genetic Linkage

Number of relevant bibliographic references: 16.

Ident.	Authors (with country if any)	Title
002A33 (2014)	Mariëlle Alders [Pays-Bas] ; Lihadh Al-Gazali ; Isabelle Cordeiro ; Bruno Dallapiccola ; Livia Garavelli ; Beyhan Tuysuz ; Faranak Salehi ; Martin A. Haagmans ; Olaf R. Mook ; Charles B. Majoie ; Marcel M. Mannens ; Raoul C. Hennekam	Hennekam syndrome can be caused by FAT4 mutations and be allelic to Van Maldergem syndrome.
005159 (2011)	Pia Ostergaard [Royaume-Uni] ; Michael A. Simpson [Royaume-Uni] ; Glen Brice [Royaume-Uni] ; Sahar Mansour [Royaume-Uni] ; Fiona C. Connell [Royaume-Uni] ; Alexandros Onoufriadis [Royaume-Uni] ; Anne H. Child [Royaume-Uni] ; Jae Hwang [Royaume-Uni] ; Kamini Kalidas [Royaume-Uni] ; Peter S. Mortimer [Royaume-Uni] ; Richard Trembath [Royaume-Uni] ; Steve Jeffery [Royaume-Uni]	Rapid identification of mutations in GJC2 in primary lymphoedema using whole exome sequencing combined with linkage analysis with delineation of the phenotype
005274 (2011)	P. Ostergaard [Royaume-Uni] ; Ma Simpson [Royaume-Uni] ; S. Jeffery [Royaume-Uni]	Massively parallel sequencing and identification of genes for primary lymphoedema: a perfect fit
005817 (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.
006B68 (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.
008315 (2005)	M Y M. Ng ; T. Andrew ; T D Spector ; S. Jeffery	Linkage to the FOXC2 region of chromosome 16 for varicose veins in otherwise healthy, unselected sibling pairs
008626 (2005)	Carolyn Sholto-Douglas-Vernon [Royaume-Uni] ; Rachel Bell [Royaume-Uni] ; Glen Brice [Royaume-Uni] ; Sahar Mansour [Royaume-Uni] ; Mansoor Sarfarazi [États-Unis] ; Anne H. Child [Royaume-Uni] ; Alberto Smith [Royaume-Uni] ; Russell Mellor [Royaume-Uni] ; Kevin Burnand [Royaume-Uni] ; Peter Mortimer (dermatologue)‎ [Royaume-Uni] ; Steve Jeffery [Royaume-Uni]	Lymphoedema-distichiasis and FOXC2 : unreported mutations, de novo mutation estimate, families without coding mutations
009943 (2001)	R. Döffinger [France] ; A. Smahi ; C. Bessia ; F. Geissmann ; J. Feinberg ; A. Durandy ; C. Bodemer ; S. Kenwrick ; S. Dupuis-Girod ; S. Blanche ; P. Wood ; S H Rabia ; D J Headon ; P A Overbeek ; F. Le Deist ; S M Holland ; K. Belani ; D S Kumararatne ; A. Fischer ; R. Shapiro ; M E Conley ; E. Reimund ; H. Kalhoff ; M. Abinun ; A. Munnich ; A. Israël ; G. Courtois ; J L Casanova	X-linked anhidrotic ectodermal dysplasia with immunodeficiency is caused by impaired NF-kappaB signaling.
009A80 (2001)	L R Osborne	'Forkhead' gene expression balanced on a knife-edge.
009E36 (2001)	Marika J. Karkkainen [Finlande] ; Lotta Jussila [Finlande] ; Kari Alitalo [Finlande] ; Robert E. Ferrell ; David N. Finegold	Molecular regulation of lymphangiogenesis and targets for tissue oedema
00A280 (2000)	S E Hong [États-Unis] ; Y Y Shugart ; D T Huang ; S A Shahwan ; P E Grant ; J O Hourihane ; N D Martin ; C A Walsh	Autosomal recessive lissencephaly with cerebellar hypoplasia is associated with human RELN mutations.
00AD75 (1999)	A. Tsezou ; Ch Hadjiathanasiou ; D. Gourgiotis ; A. Galla ; Em Kavazarakis ; A. Pasparaki ; M. Kapsetaki ; C. Sismani [Chypre (pays)] ; Ch Theodoridis ; Pc Patsalis [Chypre (pays)] ; N. Moschonas ; S. Kitsiou	Molecular genetics of Turner syndrome: correlation with clinical phenotype and response to growth hormone therapy
00B255 (1998)	Robert E. Ferrell [États-Unis] ; Kara L. Levinson [États-Unis] ; Judith H. Esman [États-Unis] ; Mark A. Kimak [États-Unis] ; Elizabeth C. Lawrence [États-Unis] ; M. Michael Barmada [États-Unis] ; David N. Finegold [États-Unis]	Hereditary Lymphedema: Evidence for Linkage and Genetic Heterogeneity
00B524 (1998)	Andrew R. Zinn [États-Unis] ; Vijay S. Tonk ; Zhong Chen ; Wendy L. Flejter ; H. Allen Gardner ; Rudy Guerra ; Harvey Kushner [États-Unis] ; Stuart Schwartz ; Virginia P. Sybert ; Daniel L. Van Dyke ; Judith L. Ross [États-Unis]	Evidence for a Turner Syndrome Locus or Loci at Xp11.2-p22.1
00C866 (1994)	D W Severson ; A. Mori ; Y. Zhang ; B M Christensen	Chromosomal mapping of two loci affecting filarial worm susceptibility in Aedes aegypti.
00F527 (1983)	Claude S. Dahlberg [États-Unis] ; Claude S. Borer [États-Unis] ; Kermit L. Newcomer [États-Unis] ; Wilfrido R. Yutuc [États-Unis]	Autosomal or X‐linked recessive syndrome of congenital lymphedema, hypoparathyroidism, nephropathy, prolapsing mitral valve, and brachytelephalangy

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