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    Results: 1 to 50 of 258

    1.

    Age-related hearing loss in four Italian genetic isolates: An epidemiological study.

    Bedin E, Franzè A, Zadro C, Persico MG, Ciullo M, Hladnik U, Dolcetta D, Grasso DL, Riccardi P, Nutile T, Andrighetto G, D'Adamo P, Gasparini P, Marciano E.

    Int J Audiol. 2009;48(7):465-472.PMID: 19925333 [PubMed - as supplied by publisher]Related articles

    2.

    Heritability and demographic analyses in the large isolated population of val borbera suggest advantages in mapping complex traits genes.

    Traglia M, Sala C, Masciullo C, Cverhova V, Lori F, Pistis G, Bione S, Gasparini P, Ulivi S, Ciullo M, Nutile T, Bosi E, Sirtori M, Mignogna G, Rubinacci A, Buetti I, Camaschella C, Petretto E, Toniolo D.

    PLoS One. 2009 Oct 22;4(10):e7554.PMID: 19847309 [PubMed - in process]Related articlesFree article

    3.

    The 2q23.1 microdeletion syndrome: clinical and behavioural phenotype.

    van Bon BW, Koolen DA, Brueton L, McMullan D, Lichtenbelt KD, Adès LC, Peters G, Gibson K, Novara F, Pramparo T, Bernardina BD, Zoccante L, Balottin U, Piazza F, Pecile V, Gasparini P, Guerci V, Kets M, Pfundt R, de Brouwer AP, Veltman JA, de Leeuw N, Wilson M, Antony J, Reitano S, Luciano D, Fichera M, Romano C, Brunner HG, Zuffardi O, de Vries BB.

    Eur J Hum Genet. 2009 Oct 7. [Epub ahead of print]PMID: 19809484 [PubMed - as supplied by publisher]Related articles

    4.

    Genetic variation in taste sensitivity to 6-n-propylthiouracil and its relationship to taste perception and food selection.

    Tepper BJ, White EA, Koelliker Y, Lanzara C, d'Adamo P, Gasparini P.

    Ann N Y Acad Sci. 2009 Jul;1170:126-39. Review.PMID: 19686122 [PubMed - indexed for MEDLINE]Related articles

    5.

    Reactive oxygen species in human inner ear perilymph.

    Ciorba A, Gasparini P, Chicca M, Pinamonti S, Martini A.

    Acta Otolaryngol. 2009 Aug 14:1-7. [Epub ahead of print]PMID: 19685356 [PubMed - as supplied by publisher]Related articles

    6.

    Quality control procedures in the Italian national forest inventory.

    Gasparini P, Bertani R, De Natale F, Di Cosmo L, Pompei E.

    J Environ Monit. 2009 Apr;11(4):761-8. Epub 2009 Mar 6.PMID: 19557227 [PubMed - in process]Related articles

    7.

    SDHAF1, encoding a LYR complex-II specific assembly factor, is mutated in SDH-defective infantile leukoencephalopathy.

    Ghezzi D, Goffrini P, Uziel G, Horvath R, Klopstock T, Lochmüller H, D'Adamo P, Gasparini P, Strom TM, Prokisch H, Invernizzi F, Ferrero I, Zeviani M.

    Nat Genet. 2009 May 24. [Epub ahead of print]PMID: 19465911 [PubMed - as supplied by publisher]Related articles

    8.

    Genetic structure of Europeans: a view from the North-East.

    Nelis M, Esko T, Mägi R, Zimprich F, Zimprich A, Toncheva D, Karachanak S, Piskácková T, Balascák I, Peltonen L, Jakkula E, Rehnström K, Lathrop M, Heath S, Galan P, Schreiber S, Meitinger T, Pfeufer A, Wichmann HE, Melegh B, Polgár N, Toniolo D, Gasparini P, D'Adamo P, Klovins J, Nikitina-Zake L, Kucinskas V, Kasnauskiene J, Lubinski J, Debniak T, Limborska S, Khrunin A, Estivill X, Rabionet R, Marsal S, Julià A, Antonarakis SE, Deutsch S, Borel C, Attar H, Gagnebin M, Macek M, Krawczak M, Remm M, Metspalu A.

    PLoS One. 2009;4(5):e5472. Epub 2009 May 8.PMID: 19424496 [PubMed - indexed for MEDLINE]Related articlesFree article

    9.

    Tumor-initiating cells of HER2-positive carcinoma cell lines express the highest oncoprotein levels and are sensitive to trastuzumab.

    Magnifico A, Albano L, Campaner S, Delia D, Castiglioni F, Gasparini P, Sozzi G, Fontanella E, Menard S, Tagliabue E.

    Clin Cancer Res. 2009 Mar 15;15(6):2010-21. Epub 2009 Mar 10.PMID: 19276287 [PubMed - indexed for MEDLINE]Related articles

    10.

    Detection of epidermal thickening in GJB2 carriers with epidermal US.

    Guastalla P, Guerci VI, Fabretto A, Faletra F, Grasso DL, Zocconi E, Stefanidou D, D'Adamo P, Ronfani L, Montico M, Morgutti M, Gasparini P.

    Radiology. 2009 Apr;251(1):280-6. Epub 2009 Feb 3.PMID: 19190252 [PubMed - indexed for MEDLINE]Related articles

    11.

    EML4-ALK rearrangement in non-small cell lung cancer and non-tumor lung tissues.

    Martelli MP, Sozzi G, Hernandez L, Pettirossi V, Navarro A, Conte D, Gasparini P, Perrone F, Modena P, Pastorino U, Carbone A, Fabbri A, Sidoni A, Nakamura S, Gambacorta M, Fernández PL, Ramirez J, Chan JK, Grigioni WF, Campo E, Pileri SA, Falini B.

    Am J Pathol. 2009 Feb;174(2):661-70. Epub 2009 Jan 15.PMID: 19147828 [PubMed - indexed for MEDLINE]Related articlesFree article

    12.

    Metabonomics and population studies: age-related amino acids excretion and inferring networks through the study of urine samples in two Italian isolated populations.

    D'Adamo P, Ulivi S, Beneduci A, Pontoni G, Capasso G, Lanzara C, Andrighetto G, Hladnik U, Nunes V, Palacin M, Gasparini P.

    Amino Acids. 2008 Dec 9. [Epub ahead of print]PMID: 19067108 [PubMed - as supplied by publisher]Related articles

    13.

    Does epidermal thickening explain GJB2 high carrier frequency and heterozygote advantage?

    D'Adamo P, Guerci VI, Fabretto A, Faletra F, Grasso DL, Ronfani L, Montico M, Morgutti M, Guastalla P, Gasparini P.

    Eur J Hum Genet. 2009 Mar;17(3):284-6. Epub 2008 Dec 3. No abstract available. PMID: 19050724 [PubMed - indexed for MEDLINE]Related articles

    14.

    Are MYO1C and MYO1F associated with hearing loss?

    Zadro C, Alemanno MS, Bellacchio E, Ficarella R, Donaudy F, Melchionda S, Zelante L, Rabionet R, Hilgert N, Estivill X, Van Camp G, Gasparini P, Carella M.

    Biochim Biophys Acta. 2009 Jan;1792(1):27-32. Epub 2008 Nov 5.PMID: 19027848 [PubMed - indexed for MEDLINE]Related articles

    15.

    Correlation of fragile histidine triad (Fhit) protein structural features with effector interactions and biological functions.

    Pichiorri F, Okumura H, Nakamura T, Garrison PN, Gasparini P, Suh SS, Druck T, McCorkell KA, Barnes LD, Croce CM, Huebner K.

    J Biol Chem. 2009 Jan 9;284(2):1040-9. Epub 2008 Nov 12.PMID: 19004824 [PubMed - indexed for MEDLINE]Related articles

    16.

    Delineation of HER2 gene status in breast carcinoma by silver in situ hybridization is reproducible among laboratories and pathologists.

    Carbone A, Botti G, Gloghini A, Simone G, Truini M, Curcio MP, Gasparini P, Mangia A, Perin T, Salvi S, Testi A, Verderio P.

    J Mol Diagn. 2008 Nov;10(6):527-36. Epub 2008 Oct 2.PMID: 18832456 [PubMed - indexed for MEDLINE]Related articlesFree article

    17.

    FASTKD2 nonsense mutation in an infantile mitochondrial encephalomyopathy associated with cytochrome c oxidase deficiency.

    Ghezzi D, Saada A, D'Adamo P, Fernandez-Vizarra E, Gasparini P, Tiranti V, Elpeleg O, Zeviani M.

    Am J Hum Genet. 2008 Sep;83(3):415-23. Epub 2008 Sep 4.PMID: 18771761 [PubMed - indexed for MEDLINE]Related articlesFree article

    18.

    A new dic(7;12)(p12.21;p12.2) chromosome aberration in a case of acute myeloid leukemia.

    Tapinassi C, Gerbino E, Malazzi O, Micucci C, Gasparini P, Najera MJ, Calasanz MJ, Odero MD, Pelicci PG, Belloni E.

    Cancer Genet Cytogenet. 2008 Sep;185(2):102-5.PMID: 18722879 [PubMed - indexed for MEDLINE]Related articles

    19.

    Variation in the bitter-taste receptor gene TAS2R38, and adiposity in a genetically isolated population in Southern Italy.

    Tepper BJ, Koelliker Y, Zhao L, Ullrich NV, Lanzara C, d'Adamo P, Ferrara A, Ulivi S, Esposito L, Gasparini P.

    Obesity (Silver Spring). 2008 Oct;16(10):2289-95. Epub 2008 Jul 24.PMID: 18719631 [PubMed - indexed for MEDLINE]Related articles

    20.

    Role of xanthine oxidase activation and reduced glutathione depletion in rhinovirus induction of inflammation in respiratory epithelial cells.

    Papi A, Contoli M, Gasparini P, Bristot L, Edwards MR, Chicca M, Leis M, Ciaccia A, Caramori G, Johnston SL, Pinamonti S.

    J Biol Chem. 2008 Oct 17;283(42):28595-606. Epub 2008 Aug 4.PMID: 18678861 [PubMed - indexed for MEDLINE]Related articlesFree article

    21.

    Cohen syndrome resulting from a novel large intragenic COH1 deletion segregating in an isolated Greek island population.

    Bugiani M, Gyftodimou Y, Tsimpouka P, Lamantea E, Katzaki E, d'Adamo P, Nakou S, Georgoudi N, Grigoriadou M, Tsina E, Kabolis N, Milani D, Pandelia E, Kokotas H, Gasparini P, Giannoulia-Karantana A, Renieri A, Zeviani M, Petersen MB.

    Am J Med Genet A. 2008 Sep 1;146A(17):2221-6.PMID: 18655112 [PubMed - indexed for MEDLINE]Related articles

    22.

    Variation of hemoglobin levels in normal Italian populations from genetic isolates.

    Sala C, Ciullo M, Lanzara C, Nutile T, Bione S, Massacane R, d'Adamo P, Gasparini P, Toniolo D, Camaschella C.

    Haematologica. 2008 Sep;93(9):1372-5. Epub 2008 Jul 4.PMID: 18603552 [PubMed - indexed for MEDLINE]Related articlesFree article

    23.

    Severe infantile encephalomyopathy caused by a mutation in COX6B1, a nucleus-encoded subunit of cytochrome c oxidase.

    Massa V, Fernandez-Vizarra E, Alshahwan S, Bakhsh E, Goffrini P, Ferrero I, Mereghetti P, D'Adamo P, Gasparini P, Zeviani M.

    Am J Hum Genet. 2008 Jun;82(6):1281-9. Epub 2008 May 22.PMID: 18499082 [PubMed - indexed for MEDLINE]Related articlesFree article

    24.

    REGgamma proteasome activator is involved in the maintenance of chromosomal stability.

    Zannini L, Lecis D, Buscemi G, Carlessi L, Gasparini P, Fontanella E, Lisanti S, Barton L, Delia D.

    Cell Cycle. 2008 Feb 15;7(4):504-12. Epub 2007 Nov 23.PMID: 18235248 [PubMed - indexed for MEDLINE]Related articles

    25.

    Photochemically enhanced delivery of a cell-penetrating peptide nucleic acid conjugate targeting human telomerase reverse transcriptase: effects on telomere status and proliferative potential of human prostate cancer cells.

    Folini M, Bandiera R, Millo E, Gandellini P, Sozzi G, Gasparini P, Longoni N, Binda M, Daidone MG, Berg K, Zaffaroni N.

    Cell Prolif. 2007 Dec;40(6):905-20.PMID: 18021178 [PubMed - indexed for MEDLINE]Related articles

    26.

    The role of chromosomal alterations in human cancer development.

    Gasparini P, Sozzi G, Pierotti MA.

    J Cell Biochem. 2007 Oct 1;102(2):320-31. Review.PMID: 17722107 [PubMed - indexed for MEDLINE]Related articles

    27.

    Relationship between p53 and p27 expression following HER2 signaling.

    Casalini P, Iorio MV, Berno V, Bergamaschi A, Børresen Dale AL, Gasparini P, Orlandi R, Casati B, Tagliabue E, Ménard S.

    Breast. 2007 Dec;16(6):597-605. Epub 2007 Jun 28.PMID: 17604627 [PubMed - indexed for MEDLINE]Related articles

    28.

    A functional study of plasma-membrane calcium-pump isoform 2 mutants causing digenic deafness.

    Ficarella R, Di Leva F, Bortolozzi M, Ortolano S, Donaudy F, Petrillo M, Melchionda S, Lelli A, Domi T, Fedrizzi L, Lim D, Shull GE, Gasparini P, Brini M, Mammano F, Carafoli E.

    Proc Natl Acad Sci U S A. 2007 Jan 30;104(5):1516-21. Epub 2007 Jan 18.PMID: 17234811 [PubMed - indexed for MEDLINE]Related articlesFree article

    29.

    Radiation effects on development of HER2-positive breast carcinomas.

    Castiglioni F, Terenziani M, Carcangiu ML, Miliano R, Aiello P, Bertola L, Triulzi T, Gasparini P, Camerini T, Sozzi G, Fossati-Bellani F, Ménard S, Tagliabue E.

    Clin Cancer Res. 2007 Jan 1;13(1):46-51.PMID: 17200337 [PubMed - indexed for MEDLINE]Related articlesFree article

    30.

    A novel t(2;3)(p11;q27) in a case of follicular lymphoma.

    Tapinassi C, Micucci C, Lahortiga I, Malazzi O, Gasparini P, Gorosquieta A, Odero MD, Belloni E.

    Cancer Genet Cytogenet. 2007 Jan 1;172(1):70-3.PMID: 17175383 [PubMed - indexed for MEDLINE]Related articles

    31.

    Oncogene-induced senescence is a DNA damage response triggered by DNA hyper-replication.

    Di Micco R, Fumagalli M, Cicalese A, Piccinin S, Gasparini P, Luise C, Schurra C, Garre' M, Nuciforo PG, Bensimon A, Maestro R, Pelicci PG, d'Adda di Fagagna F.

    Nature. 2006 Nov 30;444(7119):638-42.PMID: 17136094 [PubMed - indexed for MEDLINE]Related articles

    32.

    Exclusion of chromosome region 22q12.1-q12.3 as a second locus for Costello syndrome.

    Bertelli M, Cecchin S, Fabbri A, Lapucci C, Gasparini P.

    Panminerva Med. 2006 Jun;48(2):145-6. No abstract available. PMID: 16953153 [PubMed - indexed for MEDLINE]Related articles

    33.

    Microarray and large-scale in silico--based identification of genes functionally related to Haptoglobin and/or Hemopexin.

    Fagoonee S, Di Cunto F, Vozzi D, Volinia S, Pellegrino M, Gasparini P, Silengo L, Altruda F, Tolosano E.

    DNA Cell Biol. 2006 Jun;25(6):323-30.PMID: 16792502 [PubMed - indexed for MEDLINE]Related articles

    34.

    MPV17 encodes an inner mitochondrial membrane protein and is mutated in infantile hepatic mitochondrial DNA depletion.

    Spinazzola A, Viscomi C, Fernandez-Vizarra E, Carrara F, D'Adamo P, Calvo S, Marsano RM, Donnini C, Weiher H, Strisciuglio P, Parini R, Sarzi E, Chan A, DiMauro S, Rötig A, Gasparini P, Ferrero I, Mootha VK, Tiranti V, Zeviani M.

    Nat Genet. 2006 May;38(5):570-5. Epub 2006 Apr 2.PMID: 16582910 [PubMed - indexed for MEDLINE]Related articles

    35.

    Mitochondrial 12S rRNA gene mutations affect RNA secondary structure and lead to variable penetrance in hearing impairment.

    Ballana E, Morales E, Rabionet R, Montserrat B, Ventayol M, Bravo O, Gasparini P, Estivill X.

    Biochem Biophys Res Commun. 2006 Mar 24;341(4):950-7. Epub 2006 Jan 24.PMID: 16458854 [PubMed - indexed for MEDLINE]Related articles

    36.

    Identification of a novel mutation in the myosin VIIA motor domain in a family with autosomal dominant hearing loss (DFNA11).

    Di Leva F, D'Adamo P, Cubellis MV, D'Eustacchio A, Errichiello M, Saulino C, Auletta G, Giannini P, Donaudy F, Ciccodicola A, Gasparini P, Franzè A, Marciano E.

    Audiol Neurootol. 2006;11(3):157-64. Epub 2006 Jan 9.PMID: 16449806 [PubMed - indexed for MEDLINE]Related articles

    37.

    Dissecting clinical findings: platelet defects segregate independently of deafness and cataract in a family affected by an apparent syndromic form of macrothrombocytopenia.

    Gangarossa S, Seri M, Pecci A, Di Bari F, Cusano R, Balduini C, Gasparini P, Savoia A.

    Int J Mol Med. 2005 Sep;16(3):437-41.PMID: 16077952 [PubMed - indexed for MEDLINE]Related articles

    38.

    Stomatocytic haemolysis and macrothrombocytopenia (Mediterranean stomatocytosis/macrothrombocytopenia) is the haematological presentation of phytosterolaemia.

    Rees DC, Iolascon A, Carella M, O'marcaigh AS, Kendra JR, Jowitt SN, Wales JK, Vora A, Makris M, Manning N, Nicolaou A, Fisher J, Mann A, Machin SJ, Clayton PT, Gasparini P, Stewart GW.

    Br J Haematol. 2005 Jul;130(2):297-309.PMID: 16029460 [PubMed - indexed for MEDLINE]Related articles

    39.

    Frequent loss of heterozygosity without loss of genetic material in acute myeloid leukemia with a normal karyotype.

    Gorletta TA, Gasparini P, D'Elios MM, Trubia M, Pelicci PG, Di Fiore PP.

    Genes Chromosomes Cancer. 2005 Nov;44(3):334-7.PMID: 16015648 [PubMed - indexed for MEDLINE]Related articles

    40.

    Espin gene (ESPN) mutations associated with autosomal dominant hearing loss cause defects in microvillar elongation or organisation.

    Donaudy F, Zheng L, Ficarella R, Ballana E, Carella M, Melchionda S, Estivill X, Bartles JR, Gasparini P.

    J Med Genet. 2006 Feb;43(2):157-61. Epub 2005 Jun 1.PMID: 15930085 [PubMed - indexed for MEDLINE]Related articlesFree article

    41.

    Audiometric evaluation of carriers of the connexin 26 mutation 35delG.

    Franzé A, Caravelli A, Di Leva F, Marciano E, Auletta G, D'Aulos F, Saulino C, Esposito L, Carella M, Gasparini P.

    Eur Arch Otorhinolaryngol. 2005 Nov;262(11):921-4. Epub 2005 May 14.PMID: 15895291 [PubMed - indexed for MEDLINE]Related articles

    42.

    FISH analysis of hematological neoplasias with 1p36 rearrangements allows the definition of a cluster of 2.5 Mb included in the minimal region deleted in 1p36 deletion syndrome.

    Lahortiga I, Vázquez I, Belloni E, Román JP, Gasparini P, Novo FJ, Zudaire I, Pelicci PG, Hernández JM, Calasanz MJ, Odero MD.

    Hum Genet. 2005 May;116(6):476-85. Epub 2005 Mar 3.PMID: 15744521 [PubMed - indexed for MEDLINE]Related articles

    43.

    Autosomal recessive progressive myoclonus epilepsy with ataxia and mental retardation.

    Coppola G, Criscuolo C, De Michele G, Striano S, Barbieri F, Striano P, Perretti A, Santoro L, Brescia Morra V, Saccà F, Scarano V, D'Adamo AP, Banfi S, Gasparini P, Santorelli FM, Lehesjoki AE, Filla A.

    J Neurol. 2005 Aug;252(8):897-900. Epub 2005 Mar 8.PMID: 15742102 [PubMed - indexed for MEDLINE]Related articles

    44.

    [A double blind randomised clinical trial to assess the efficacy of the treatments of the superficial pressure sores]

    Di Giulio P, Saiani L, Laquintana D, Palese A, Perli S, Andreatta M, Rosa F, Chini P, Soraperra F, Ventura I, Suriani C, Romani S, Zancarli M, Martini M, Partel F, Bassetti S, Kaisermann R, Bortolotti C, Gianordoli M, Rizzoli I, Nardelli R, Pellizzari E, Valduga E, Castaman M, Pordenon M, Beltrame M, Bertolo C, Casasola E, Del Pin P, Giolo S, Marcatti E, Pecini D, Rodaro M, Zanon C, Stefanon L, Covre L, Babbo C, Martin I, Roilo A, Zanutel M, Sabbadin S, Boin L, Caron A, Martignago E, Venturin V, Greggio A, Frigo P, Lazzaron D, Tonietto A, Zanin B, Zorzi S, Zuanon A, Salmaso D, Frison T, Marin I, Buosi A, Fiorese E, Gasparin D, Goat B, Saccardo G, Simonetto O, Gomiero S, Baccara N, Ghirardello L, Niolu M, Silvestri S, Buffon ML, Casson P, Santantonio R, Albore P, Mazzorana E, Terziariol L, Bulgarelli G, Barani E, Gasparini P, Migliori S, Sasso E, Marfisi RM, Tognoni G, Sgaroni G, Noro G, Mattiuzzo M; Gruppo PARI-ETLD.

    Assist Inferm Ric. 2004 Oct-Dec;23(4):201-8. Italian. Erratum in: Assist Inferm Ric. 2005 Jan-Mar;24(1):51. Mattiuzzo, Mara [added]. PMID: 15709463 [PubMed - indexed for MEDLINE]Related articles

    45.

    A novel GJA1 mutation causes oculodentodigital dysplasia without syndactyly.

    Vitiello C, D'Adamo P, Gentile F, Vingolo EM, Gasparini P, Banfi S.

    Am J Med Genet A. 2005 Feb 15;133A(1):58-60.PMID: 15637728 [PubMed - indexed for MEDLINE]Related articles

    46.

    8p11 myeloproliferative syndrome with a novel t(7;8) translocation leading to fusion of the FGFR1 and TIF1 genes.

    Belloni E, Trubia M, Gasparini P, Micucci C, Tapinassi C, Confalonieri S, Nuciforo P, Martino B, Lo-Coco F, Pelicci PG, Di Fiore PP.

    Genes Chromosomes Cancer. 2005 Mar;42(3):320-5.PMID: 15609342 [PubMed - indexed for MEDLINE]Related articles

    47.

    Guidelines and recommendations for testing of Cx26 mutations and interpretation of results.

    Mazzoli M, Newton V, Murgia A, Bitner-Glindzicz M, Gasparini P, Read A, Parving A.

    Int J Pediatr Otorhinolaryngol. 2004 Nov;68(11):1397-8. No abstract available. PMID: 15488970 [PubMed - indexed for MEDLINE]Related articles

    48.

    A second locus mapping to 2q35-36 for familial pseudohyperkalaemia.

    Carella M, d'Adamo AP, Grootenboer-Mignot S, Vantyghem MC, Esposito L, D'Eustacchio A, Ficarella R, Stewart GW, Gasparini P, Delaunay J, Iolascon A.

    Eur J Hum Genet. 2004 Dec;12(12):1073-6.PMID: 15470366 [PubMed - indexed for MEDLINE]Related articlesFree article

    49.

    Genes transcriptionally modulated by interferon alpha2a correlate with the cytokine activity.

    Iolascon A, Volinia S, Borriello A, Giordani L, Moretti A, Servedio V, Maiorano N, Cucciolla V, Criniti V, Gasparini P, Indaco S, Della Ragione F.

    Haematologica. 2004 Sep;89(9):1046-53.PMID: 15377465 [PubMed - indexed for MEDLINE]Related articlesFree article

    50.

    Mitochondrial DNA mutations in patients with postlingual, nonsyndromic hearing impairment.

    Jacobs HT, Hutchin TP, Käppi T, Gillies G, Minkkinen K, Walker J, Thompson K, Rovio AT, Carella M, Melchionda S, Zelante L, Gasparini P, Pyykkö I, Shah ZH, Zeviani M, Mueller RF.

    Eur J Hum Genet. 2005 Jan;13(1):26-33.PMID: 15292920 [PubMed - indexed for MEDLINE]Related articlesFree article

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