Genesis healthcare corporation < Genet < Genet byers

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List of bibliographic references

Number of relevant bibliographic references: 66.
[0-20] [0 - 20][0 - 50][20-40]

Ident.	Authors (with country if any)	Title
000120 (2006)	Ts Roberts [Afrique du Sud] ; L. Stephen [Afrique du Sud] ; P. Beighton [Afrique du Sud]	Osteoglophonic dysplasia: dental and orthodontic implications
000407 (2004)	Akio Kikuchi [Japon] ; Atsushi Takeda [Japon] ; Kazuo Fujihara [Japon] ; Teiko Kimpara [Japon] ; Yusei Shiga [Japon] ; Hiroaki Tanji [Japon] ; Makiko Nagai [Japon] ; Hiroshi Ichinose [Japon] ; Fumi Urano [Japon] ; Nobuyuki Okamura [Japon] ; Hiroyuki Arai [Japon] ; Yasuto Itoyama [Japon]	Arg(184)his mutant GTP cyclohydrolase I, causing recessive hyperphenylalaninemia, is responsible for dopa‐responsive dystonia with parkinsonism: A case report
000442 (1991)	Carol J. Ludowese [États-Unis] ; Kate J. Thompson [États-Unis] ; Gurbax S. Sekhon [États-Unis] ; Richard M. Pauli [États-Unis]	Absence of predictable phenotypic expression in proximal 15q duplications
000614 (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
000696 (2010)	Arti Nanda ; Wafa A. Al-Ateeqi ; Mona A. Al-Khawari ; Qasem A. Alsaleh ; Jeoram T. Anim [Koweït]	GAPO Syndrome: A Report of Two Siblings and a Review of Literature
000702 (2001)	Rudolf Happle [Allemagne]	Genetic hair loss
000898 (1998)	P. A. Mossey [Royaume-Uni] ; J. Mccoll [Royaume-Uni] ; M. O'Hara [Royaume-Uni]	Cephalometric features in the parents of children with orofacial clefting
000A16 (1998)	Alan Shanske [États-Unis] ; Issac Sachmechi [États-Unis] ; Dinesh K. Patel [États-Unis] ; Alka Bishnoi [États-Unis] ; Fred Rosner [États-Unis]	An adult with 49,XYYYY karyotype: Case report and endocrine studies
000D10 (1996)	Alain Verloes [Belgique] ; Paul Jamblin [Belgique] ; Lucien Koulischer [Belgique] ; Jean-Pierre Bourguignon [Belgique]	A new form of skeletal dysplasia with amelogenesis imperfecta and platyspondyly
000D76 (1990)	R. Gershoni-Baruch [Israël] ; E. V. Moor [Israël] ; R. Enat [Israël]	Marfan syndrome associated with bicuspid aortic valve, premature aging, and primary hypogonadism
001378 (2002)	Alasdair G. W. Hunter [Canada]	Coffin‐Lowry syndrome: A 20‐year follow‐up and review of long‐term outcomes
001556 (2001)		Current Awareness
001759 (2011)	Warissara Sripathomsawat [Thaïlande] ; Pranoot Tanpaiboon [Thaïlande] ; Jan Heering [Allemagne] ; Volker Dötsch [Allemagne] ; Raoul C. M. Hennekam [Pays-Bas] ; Piranit Kantaputra [Thaïlande]	Phenotypic analysis of Arg227 mutations of TP63 with emphasis on dental phenotype and micturition difficulties in EEC syndrome
001869 (2013)	Ginevra Zanni [Italie] ; John M. Opitz [États-Unis]	Annals of morphology. Atavisms: Phylogenetic lazarus?
001A61 (1991)	A. Clarke ; J. Burn	Sweat testing to identify female carriers of X linked hypohidrotic ectodermal dysplasia.
001D99 (2013)	T. Nguyen [États-Unis] ; C. Phillips [États-Unis] ; S. Frazier-Bower [États-Unis] ; T. Wright [États-Unis]	Craniofacial variations in the tricho‐dento‐osseous syndrome
002450 (1985)	Anna-Lisa Söderholm [Finlande] ; Ilkka Kaitila [Finlande]	Expression of X‐linked hypohidrotic ectodermal dysplasia in six males and in their mothers
002471 (2008)	Marianna Bugiani [Italie] ; Yolanda Gyftodimou [Grèce] ; Paraskevi Tsimpouka [Grèce] ; Eleonora Lamantea [Italie] ; Eleni Katzaki [Italie] ; Pio D'Adamo [Italie] ; Sheena Nakou [Grèce] ; Nelli Georgoudi [Grèce] ; Maria Grigoriadou [Grèce] ; Efthymia Tsina [Grèce] ; Nikolaos Kabolis [Grèce] ; Donatella Milani [Italie] ; Efthimia Pandelia [Grèce] ; Haris Kokotas [Grèce] ; Paolo Gasparini [Italie] ; Aglaia Giannoulia-Karantana [Grèce] ; Alessandra Renieri [Italie] ; Massimo Zeviani [Italie] ; Michael B. Petersen [Grèce]	Cohen syndrome resulting from a novel large intragenic COH1 deletion segregating in an isolated Greek island population
002571 (2001)	Uwe Kornak [Allemagne] ; Dagmar Kasper [Allemagne] ; Michael R. Bösl [Allemagne] ; Edelgard Kaiser [Allemagne] ; Michaela Schweizer [Allemagne] ; Ansgar Schulz [Allemagne] ; Wilhelm Friedrich [Allemagne] ; Günter Delling [Allemagne] ; Thomas J. Jentsch [Allemagne]	Loss of the ClC-7 Chloride Channel Leads to Osteopetrosis in Mice and Man
002581 (1977)	A. G. W. Hunter [Canada] ; M. Ray [Canada] ; H. S. Wang [Canada] ; D. R. Thompson [Canada]	Phenotypic correlations in patients with ring chromosome 22
002771 (2011)	Rubén Cabanillas [Espagne] ; Juan Cadi Anos [Espagne] ; José A. F. Villameytide [Espagne] ; Mercedes Pérez [Espagne] ; Jesús Longo [Espagne] ; José M. Richard [Espagne] ; Rebeca Álvarez [Espagne] ; Noelia S. Durán [Espagne] ; Rafael Illán [Espagne] ; Daniel J. González [Espagne] ; Carlos L Pez-Otín [Espagne]	Néstor–Guillermo progeria syndrome: A novel premature aging condition with early onset and chronic development caused by BANF1 mutations

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