Autoset < Autosomal < Autosomal recessive

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List of bibliographic references indexed by Autosomal

Number of relevant bibliographic references: 57.
[0-20] [0 - 20][0 - 50][20-40]

Ident.	Authors (with country if any)	Title
002973 (2013)		Poster Sessions
002974 (2013)		Poster Presentations
002A13 (2013)	M. Adachi [Japon] ; T. Iwai [Japon] ; K. Watanuki [Japon] ; G. Masuda [Japon] ; I. Tohnai [Japon]	Osteomyelitis of the jaws associated with osteopetrosis: case report of two sisters
002A97 (2013)	L. Nibali [Royaume-Uni] ; A. Medlar [Royaume-Uni] ; H. Stanescu [Royaume-Uni] ; R. Kleta [Royaume-Uni] ; U. Darbar [Royaume-Uni] ; N. Donos [Royaume-Uni]	Linkage analysis confirms heterogeneity of hereditary gingival fibromatosis
002C67 (2013)	Martyn T. Cobourne [Royaume-Uni] ; Paul T. Sharpe [Royaume-Uni]	Diseases of the tooth: the genetic and molecular basis of inherited anomalies affecting the dentition
002C71 (2013)	Ophir D. Klein ; Snehlata Oberoi ; Ann Huysseune ; Maria Hovorakova ; Miroslav Peterka ; Renata Peterkova	Developmental disorders of the dentition: An update
002D92 (2013)		Abstracts ‐ AAPA Presentations
004580 (2011)		Poster Sessions
004670 (2011)	Xiu-Ping Wang [États-Unis] ; Jiabing Fan [États-Unis]	Molecular genetics of supernumerary tooth formation
004893 (2011)	S. Beiraghi [États-Unis] ; V. Leon-Salazar [États-Unis] ; Be Larson ; Mt John [États-Unis] ; Ml Cunningham [États-Unis] ; A. Petryk [États-Unis] ; Jl Lohr [États-Unis]	Craniofacial and intraoral phenotype of Robinow syndrome forms
004995 (2011)		Abstracts of AAPA poster and podium presentations
005037 (2010)	S. A. Schneider [Royaume-Uni, Allemagne] ; K. P. Bhatia [Royaume-Uni]	Secondary dystonia – clinical clues and syndromic associations
005A84 (2009)		Poster Sessions
006F58 (2006)	Mônica Fernandes Gomes [Brésil] ; Daniela Coelho Rangel [Brésil] ; Cláudia Cristina Morais Starling [Brésil] ; Maria Graças Vilela Goulart [Brésil]	Familial malignant osteopetrosis in children: a case report
007432 (2005)		Oral presentations
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
007501 (2005)	Alan R. Templeton [États-Unis]	Haplotype Trees and Modern Human Origins
007871 (2004)	Christoph Schrader [Allemagne] ; Thomas Peschel [Allemagne] ; Michael Petermeyer [Allemagne] ; Reinhard Dengler [Allemagne] ; Dieter Hellwig [Allemagne]	Unilateral deep brain stimulation of the internal globus pallidus alleviates tardive dyskinesia
007903 (2004)	Renato P. Munhoz [Canada] ; Catherine Bergeron [Canada] ; Anthony E. Lang [Canada]	Sporadic case of dentatorubral pallidoluysian atrophy with no CAG repeat expansion and no intranuclear inclusions
007911 (2004)	John Yianni [Royaume-Uni] ; Dipankar Nandi [Royaume-Uni] ; Kevin Bradley [Royaume-Uni] ; Nigel Soper [Royaume-Uni] ; Ralph Gregory [Royaume-Uni] ; Carole Joint [Royaume-Uni] ; John Stein [Royaume-Uni] ; Richard Scott [Royaume-Uni] ; Tipu Aziz [Royaume-Uni]	Senile chorea treated by deep brain stimulation—A clinical, neurophysiological and functional imaging study
007914 (2004)	Alastair Wilkins [Royaume-Uni] ; Jerry M. Brown [Royaume-Uni] ; Roger A. Barker [Royaume-Uni]	SCA2 presenting as levodopa‐responsive parkinsonism in a young patient from the United Kingdom: A case report

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