0022-2585 < 0022-2593 < 0022-2615

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List of bibliographic references indexed by 0022-2593

Number of relevant bibliographic references: 18.

Ident.	Authors (with country if any)	Title
004F08 (2010)	Arne S. Schaefer [Allemagne] ; Gesa M. Richter [Allemagne] ; Henrik Dommisch [Allemagne] ; Markus Reinartz [Allemagne] ; Michael Nothnagel [Allemagne] ; Barbara Noack [Allemagne] ; Marja L. Laine [Pays-Bas] ; Mathias Folwaczny [Allemagne] ; Birte Groessner-Schreiber [Allemagne] ; Bruno G. Loos [Pays-Bas] ; S Ren Jepsen [Allemagne] ; Stefan Schreiber [Allemagne]	CDKN2BAS is associated with periodontitis in different European populations and is activated by bacterial infection
005F49 (2008)	F E Abidi [États-Unis] ; L. Holloway [États-Unis] ; C A Moore [États-Unis] ; D D Weaver [États-Unis] ; R J Simensen [États-Unis] ; R E Stevenson [États-Unis] ; R C Rogers [États-Unis] ; C E Schwartz [États-Unis]	Mutations in JARID1C are associated with X-linked mental retardation, short stature and hyperreflexia
007476 (2005)	J-W Kim [États-Unis] ; J P Simmer [États-Unis] ; T C Hart ; P S Hart ; M D Ramaswami ; J D Bartlett ; J C-C Hu [États-Unis]	MMP-20 mutation in autosomal recessive pigmented hypomaturation amelogenesis imperfecta
009369 (1999)	Pekka Arvio ; Maria Arvio ; Matti Kero ; Sinikka Pirinen ; Pirjo-Liisa Lukinmaa	Overgrowth of oral mucosa and facial skin, a novel feature of aspartylglucosaminuria
009693 (1998)	P A Mossey ; R. Arngrimsson ; J. Mccoll ; G M Vintiner ; J M Connor	Prediction of liability to orofacial clefting using genetic and craniofacial data from parents.
009C24 (1997)	N. Flanagan ; W J O'Connor ; B. Mccartan ; S. Miller ; J. Mcmenamin ; R. Watson	Developmental enamel defects in tuberous sclerosis: a clinical genetic marker?
00A478 (1995)	N. Thakker ; R. Davies ; K. Horner ; J. Armstrong ; T. Clancy ; S. Guy ; R. Harris ; P. Sloan ; G. Evans	The dental phenotype in familial adenomatous polyposis: diagnostic application of a weighted scoring system for changes on dental panoramic radiographs.
00AD72 (1993)	D G Evans ; E J Ladusans ; S. Rimmer ; L D Burnell ; N. Thakker ; P A Farndon	Complications of the naevoid basal cell carcinoma syndrome: results of a population based study.
00B442 (1991)	A C Nicholls ; J. Oliver ; D V Renouf ; M. Keston ; F M Pope	Substitution of cysteine for glycine at residue 415 of one allele of the alpha 1(I) chain of type I procollagen in type III/IV osteogenesis imperfecta.
00B584 (1991)	A. Clarke ; J. Burn	Sweat testing to identify female carriers of X linked hypohidrotic ectodermal dysplasia.
00B784 (1990)	I R Walpole ; A. Hockey ; A. Nicoll	The Nance-Horan syndrome.
00B936 (1990)	J. Goodship ; S. Malcolm ; A. Clarke ; M E Pembrey	Possible genetic heterogeneity in X linked hypohidrotic ectodermal dysplasia.
00BC08 (1989)	J. Christodoulou ; P N Mcdougall ; L J Sheffield	Choanal atresia as a feature of ectrodactyly-ectodermal dysplasia-clefting (EEC) syndrome.
00CA13 (1985)	E. Thompson ; M. Pembrey ; J M Graham	Phenotypic variation in LADD syndrome.
00D681 (1981)	P. Beighton	Familial dentinogenesis imperfecta, blue sclerae, and wormian bones without fractures: another type of osteogenesis imperfecta?
00E481 (1973)	D. C. Wallace ; K. J. Murphy ; L. Kelly ; W. H. Ward	The Basal Cell Naevus Syndrome: Report of a Family with Anosmia and a Case of Hypogonadotrophic Hypopituitarism
00E532 (1973)	Henry Hunter ; Roger Quaife	A 48,XYYY Male: A Somatic and Psychiatric Description
00EE50 (1966)	C B Kerr ; R S Wells ; K E Cooper	Gene effect in carriers of anhidrotic ectodermal dysplasia.

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