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La ricerca find articoli where soggetti phrase all words 'LEMLI-OPITZ SYNDROME' sort by level,fasc_key/DESCEND, pagina_ini_num/ASCEND ha restituito 231 riferimenti
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    1. Kelley, RI
      Inborn errors of sterol biosynthesis

      ANNUAL REVIEW OF GENOMICS AND HUMAN GENETICS
    2. Wilkie, AOM; Morriss-Kay, GM
      Genetics of craniofacial development and malformation

      NATURE REVIEWS GENETICS
    3. Sugawara, T; Fujimoto, Y; Ishibashi, T
      Molecular cloning and structural analysis of human sterol C5 desaturase

      BIOCHIMICA ET BIOPHYSICA ACTA-MOLECULAR AND CELL BIOLOGY OF LIPIDS
    4. Nwokoro, NA; Wassif, CA; Porter, FD
      Genetic disorders of cholesterol biosynthesis in mice and humans

      MOLECULAR GENETICS AND METABOLISM
    5. Battaile, KP; Battaile, BC; Merkens, LS; Maslen, CL; Steiner, RD
      Carrier frequency of the common mutation IVS8-IG > C in DHCR7 and estimateof the expected incidence of Smith-Lemli-Opitz syndrome

      MOLECULAR GENETICS AND METABOLISM
    6. Woollett, LA
      Fetal lipid metabolism

      FRONTIERS IN BIOSCIENCE
    7. Johnson, DW
      Analysis of alcohols, as dimethylglycine esters, by electrospray ionization tandem mass spectrometry

      JOURNAL OF MASS SPECTROMETRY
    8. Witsch-Baumgartner, M; Loffler, J; Utermann, G
      Mutations in the human DHCR7 gene

      HUMAN MUTATION
    9. Gofflot, F; Gaoua, W; Bourguignon, L; Roux, C; Picard, JJ
      Expression of Sonic Hedgehog downstream genes is modified in rat embryos exposed in utero to a distal inhibitor of cholesterol biosynthesis

      DEVELOPMENTAL DYNAMICS
    10. Garcia-Roman, N; Alvarez, AM; Toro, MJ; Montes, A; Lorenzo, MJ
      Lovastatin induces apoptosis of spontaneously immortalized rat brain neuroblasts: Involvement of nonsterol isoprenoid biosynthesis inhibition

      MOLECULAR AND CELLULAR NEUROSCIENCE
    11. Houten, SM; Koster, J; Romeijn, GJ; Frenkel, J; Di Rocco, M; Caruso, U; Landrieu, P; Kelley, RI; Kuis, W; Poll-The, BT; Gibson, KM; Wanders, RJA; Waterham, HR
      Organization of the mevalonate kinase (MVK) gene and identification of novel mutations causing mevalonic aciduria and hyperimmunoglobulinaemia D and periodic fever syndrome

      EUROPEAN JOURNAL OF HUMAN GENETICS
    12. Anstey, A
      Photomedicine: lessons from the Smith-Lemli-Opitz syndrome

      JOURNAL OF PHOTOCHEMISTRY AND PHOTOBIOLOGY B-BIOLOGY
    13. Souka, AP; Krampl, E; Bakalis, S; Heath, V; Nicolaides, KH
      Outcome of pregnancy in chromosomally normal fetuses with increased nuchaltranslucency in the first trimester

      ULTRASOUND IN OBSTETRICS & GYNECOLOGY
    14. Woollett, LA
      The origins and roles of cholesterol and fatty acids in the fetus

      CURRENT OPINION IN LIPIDOLOGY
    15. Dietschy, JM; Turley, SD
      Cholesterol metabolism in the brain

      CURRENT OPINION IN LIPIDOLOGY
    16. Seo, KW; Kelley, RI; Okano, S; Watanabe, T
      Mouse Td(ho) abnormality results from double point mutations of the emopamil binding protein gene (Ebp)

      MAMMALIAN GENOME
    17. Herz, J
      The LDL receptor gene family: (Un)expected signal transducers in the brain

      NEURON
    18. Wolf, C; Koumanov, K; Tenchov, B; Quinn, PJ
      Cholesterol favors phase separation of sphingomyelin

      BIOPHYSICAL CHEMISTRY
    19. Meyer, D; Maritz, FJ; Liebenberg, PH; Parkin, DP; Burgess, LJ
      Cortical lens opacities in the young patient - An indication for a lipogram?

      SOUTH AFRICAN MEDICAL JOURNAL
    20. Masturzo, B; Hyett, JA; Kalache, KD; Rumsby, G; Jauniaux, E; Rodeck, CH
      Increased nuchal translucency as a prenatal manifestation of congenital adrenal hyperplasia

      PRENATAL DIAGNOSIS
    21. Shackleton, CHL; Roitman, E; Kratz, L; Kelley, R
      Dehydro-oestriol and dehydropregnanetriol are candidate analytes for prenatal diagnosis of Smith-Lemli-Opitz syndrome

      PRENATAL DIAGNOSIS
    22. Witters, I; Moerman, P; Muenke, M; Van Assche, FA; Devriendt, K; Legius, E; Van Schoubroeck, D; Fryns, JP
      Semilobar holoprosencephaly in a 46,XY female fetus

      PRENATAL DIAGNOSIS
    23. Haas, D; Kelley, RI; Hoffmann, GF
      Inherited disorders of cholesterol biosynthesis

      NEUROPEDIATRICS
    24. Hennekam, RCM; Waterham, HR; Wanders, RJA; Aronson, DC
      No cholesterol metabolism anomalies detectable in infants with hypertrophic pyloric stenosis

      AMERICAN JOURNAL OF MEDICAL GENETICS
    25. Tierney, E; Nwokoro, NA; Porter, FD; Freund, LS; Ghuman, JK; Kelley, RI
      Behavior phenotype in the RSH/Smith-Lemli-Opitz syndrome

      AMERICAN JOURNAL OF MEDICAL GENETICS
    26. Bellini, C; Bonioli, E; Josso, N; Belville, C; Mazzella, M; Costabel, S; Sementa, AR; Marino, CE; Toma, P; Hennekam, RCM; Serra, G
      Persistence of Mullerian derivatives and intestinal lymphangiectasis in two newborn brothers: Confirmation of the Urioste syndrome

      AMERICAN JOURNAL OF MEDICAL GENETICS
    27. Nowaczyk, MJM; Siu, VM; Krakowiak, PA; Porter, FD
      Adrenal insufficiency and hypertension in a newborn infant with Smith-Lemli-Opitz syndrome

      AMERICAN JOURNAL OF MEDICAL GENETICS
    28. Nowaczyk, MJM; Farrell, SA; Sirkin, WL; Velsher, L; Krakowiak, PA; Waye, JS; Porter, FD
      Smith-Lemli-Opitz (RHS) syndrome: Holoprosencephaly and homozygous IVS8-1G-> C genotype

      AMERICAN JOURNAL OF MEDICAL GENETICS
    29. Nowaczyk, MJM; Nakamura, LM; Eng, B; Porter, FD; Waye, JS
      Frequency and ethnic distribution of the common DHCR7 mutation in Smith-Lemli-Opitz syndrome

      AMERICAN JOURNAL OF MEDICAL GENETICS
    30. Nowaczyk, MJM; McCaughey, D; Whelan, DT; Porter, FD
      Incidence of Smith-Lemli-Opitz syndrome in Ontario, Canada

      AMERICAN JOURNAL OF MEDICAL GENETICS
    31. Witsch-Baumgartner, M; Loeffler, J; Menzel, HJ; Utermann, G; Neuhaus, C
      Mutation screening in the DHCR7 gene of patients with attention deficit and hyperactivity disorder

      AMERICAN JOURNAL OF MEDICAL GENETICS
    32. Nowaczyk, MJM; Heshka, T; Eng, B; Feigenbaum, AJ; Waye, JS
      DHCR7 genotypes of cousins with Smith-Lemli-Opitz syndrome

      AMERICAN JOURNAL OF MEDICAL GENETICS
    33. Nowaczyk, MJM; Nakamura, LM; Waye, JS
      DHCR7 and Smith-Lemli-Opitz syndrome

      CLINICAL AND INVESTIGATIVE MEDICINE-MEDECINE CLINIQUE ET EXPERIMENTALE
    34. Opitz, JM
      A little cholesterol in time ....

      CLINICAL AND INVESTIGATIVE MEDICINE-MEDECINE CLINIQUE ET EXPERIMENTALE
    35. Beby-Defaux, A; Maille, L; Chabot, S; Nassimi, A; Oriot, D; Agius, G
      Fatal adenovirus type 7b infection in a child with Smith-Lemli-Opitz syndrome

      JOURNAL OF MEDICAL VIROLOGY
    36. Snijders, R
      First-trimester ultrasound

      CLINICS IN PERINATOLOGY
    37. Nissenkorn, A; Michelson, M; Ben-Zeev, B; Lerman-Sagie, T
      Inborn errors of metabolism - A cause of abnormal brain development

      NEUROLOGY
    38. Haave, NC; Innis, SM
      Cholesterol synthesis and accretion within various tissues of the fetal and neonatal rat

      METABOLISM-CLINICAL AND EXPERIMENTAL
    39. Boehmer, ALM; Nijman, RJM; Lammers, BAS; De Coninck, SJF; Van Hemel, JO; Themmen, APN; Mureau, MAM; De Jong, FH; Brinkmann, AO; Niermeijer, MF; Drop, SLS
      Etiological studies of severe or familial hypospadias

      JOURNAL OF UROLOGY
    40. Amiel, J; Lyonnet, S
      Hirschsprung disease, associated syndromes, and genetics: a review

      JOURNAL OF MEDICAL GENETICS
    41. Lindenthal, B; Aldaghlas, TA; Kelleher, JK; Henkel, SM; Tolba, R; Haidl, G; von Bermann, K
      Neutral sterols of rat epididymis: high concentrations of dehydrocholesterols in rat caput epididymidis

      JOURNAL OF LIPID RESEARCH
    42. McConihay, JA; Horn, PS; Woollett, LA
      Effect of maternal hypercholesterolemia on fetal sterol metabolism in the Golden Syrian hamster

      JOURNAL OF LIPID RESEARCH
    43. Johnson, DW; ten Brink, HJ; Jakobs, C
      A rapid screening procedure for cholesterol and dehydrocholesterol by electrospray ionization tandem mass spectrometry

      JOURNAL OF LIPID RESEARCH
    44. Salero, E; Perez-Sen, R; Aruga, J; Gimenez, C; Zafra, F
      Transcription factors Zic1 and Zic2 bind and transactivate the apolipoprotein E gene promoter

      JOURNAL OF BIOLOGICAL CHEMISTRY
    45. Kim, JH; Lee, JN; Paik, YK
      Cholesterol biosynthesis from lanosterol - A concerted role for Sp1 and NF-Y-binding sites for sterol-mediated regulation of rat 7-dehydrocholesterolreductase gene expression

      JOURNAL OF BIOLOGICAL CHEMISTRY
    46. Nowaczyk, MJM; Waye, JS
      The Smith-Lemli-Opitz syndrome: a novel metabolic way of understanding developmental biology, embryogenesis, and dysmorphology

      CLINICAL GENETICS
    47. Chace, DH
      Mass spectrometry in the clinical laboratory

      CHEMICAL REVIEWS
    48. Azurdia, RM; Anstey, AV; Rhodes, LE
      Cholesterol supplementation objectively reduces photosensitivity in the Smith-Lemli-Opitz syndrome

      BRITISH JOURNAL OF DERMATOLOGY
    49. Serfis, AB; Brancato, S; Fliesler, SJ
      Comparative behavior of sterols in phosphatidylcholine-sterol monolayer films

      BIOCHIMICA ET BIOPHYSICA ACTA-BIOMEMBRANES
    50. Hegele, RA
      Monogenic dyslipidemias: Window on determinants of plasma lipoprotein metabolism

      AMERICAN JOURNAL OF HUMAN GENETICS
    51. Waterham, HR; Koster, J; Romeijn, GJ; Hennekam, RCM; Vreken, P; Andersson, HC; FitzPatrick, DR; Kelley, RI; Wanders, RJA
      Mutations in the 3 beta-hydroxysterol Delta(24)-reductase gene cause desmosterolosis, an autosomal recessive disorder of cholesterol biosynthesis

      AMERICAN JOURNAL OF HUMAN GENETICS
    52. Nanni, L; Schelper, RL; Muenke, M
      Molecular genetics of holoprosencephaly

      PEDIATRIC PATHOLOGY & MOLECULAR MEDICINE
    53. Incardona, JP; Roelink, H
      The role of cholesterol in Shh signaling and teratogen-induced holoprosencephaly

      CELLULAR AND MOLECULAR LIFE SCIENCES
    54. Houten, SM; Wanders, RJA; Waterham, HR
      Biochemical and genetic aspects of mevalonate kinase and its deficiency

      BIOCHIMICA ET BIOPHYSICA ACTA-MOLECULAR AND CELL BIOLOGY OF LIPIDS
    55. Schoonjans, K; Brendel, C; Mangelsdorf, D; Auwerx, J
      Sterols and gene expression: control of affluence

      BIOCHIMICA ET BIOPHYSICA ACTA-MOLECULAR AND CELL BIOLOGY OF LIPIDS
    56. Mann, RK; Beachy, PA
      Cholesterol modification of proteins

      BIOCHIMICA ET BIOPHYSICA ACTA-MOLECULAR AND CELL BIOLOGY OF LIPIDS
    57. Herman, GE
      X-linked dominant disorders of cholesterol biosynthesis in man and mouse

      BIOCHIMICA ET BIOPHYSICA ACTA-MOLECULAR AND CELL BIOLOGY OF LIPIDS
    58. Nanni, L; Schelper, RL; Muenke, M
      Molecular genetics of holoprosencephaly

      FRONTIERS IN BIOSCIENCE
    59. Muenke, M; Cohen, MM
      Genetic approaches to understanding brain development: Holoprosencephaly as a model

      MENTAL RETARDATION AND DEVELOPMENTAL DISABILITIES RESEARCH REVIEWS
    60. Moebius, FF; Fitzky, BU; Glossmann, H
      Genetic defects in postsqualene cholesterol biosynthesis

      TRENDS IN ENDOCRINOLOGY AND METABOLISM
    61. Chiurazzi, P; Oostra, BA
      Genetics of mental retardation

      CURRENT OPINION IN PEDIATRICS
    62. Tercanli, S; Uyanik, G; Hosli, I; Cagdas, A; Holzgreve, W
      Increased nuchal translucency in a case of long-chain 3-hydroxyacyl-coenzyme A dehydrogenase deficiency

      FETAL DIAGNOSIS AND THERAPY
    63. Shearman, AM; Ordovas, JM; Cupples, LA; Schaefer, EJ; Harmon, MD; Shao, YJ; Keen, JD; DeStefano, AL; Joost, O; Wilson, PWF; Housman, DE; Myers, RH
      Evidence for a gene influencing the TG/HDL-C ratio on chromosome 7q32.3-qter: a genome-wide scan in the Framingham Study

      HUMAN MOLECULAR GENETICS
    64. Yu, HW; Lee, MH; Starck, L; Elias, ER; Irons, M; Salen, G; Patel, SB; Tint, GS
      Spectrum of Delta(7)-dehydrocholesterol reductase mutations in patients with the Smith-Lemli-Opitz (RSH) syndrome

      HUMAN MOLECULAR GENETICS
    65. Choe, S; Tanaka, A; Noguchi, T; Fujioka, S; Takatsuto, S; Ross, AS; Tax, FE; Yoshida, S; Feldman, KA
      Lesions in the sterol Delta(7) reductase gene of Arabidopsis cause dwarfism due to a block in brassinosteroid biosynthesis

      PLANT JOURNAL
    66. Incardona, JP; Eaton, S
      Cholesterol in signal transduction

      CURRENT OPINION IN CELL BIOLOGY
    67. Hebrok, M; Kim, SK; St-Jacques, B; McMahon, AP; Melton, DA
      Regulation of pancreas development by hedgehog signaling

      DEVELOPMENT
    68. Jang, JC; Fujioka, S; Tasaka, M; Seto, H; Takatsuto, S; Ishii, A; Aida, M; Yoshida, S; Sheen, J
      A critical role of sterols in embryonic patterning and meristem programming revealed by the fackel mutants of Arabidopsis thaliana

      GENES & DEVELOPMENT
    69. Frenkel, J; Houten, SM; Waterham, HR; Wanders, RJA; Rijkers, GT; Kimpen, JLL; Duran, R; Poll-The, BT; Kuis, W
      Mevalonate kinase deficiency and Dutch type periodic fever

      CLINICAL AND EXPERIMENTAL RHEUMATOLOGY
    70. Fliesler, SJ; Richards, MJ; Miller, CY; Peachey, NS; Cenedella, RJ
      Retinal structure and function in an animal model that replicates the biochemical hallmarks of desmosterolosis

      NEUROCHEMICAL RESEARCH
    71. Wolf, C; Chachaty, C
      Compared effects of cholesterol and 7-dehydrocholesterol on sphingomyelin-glycerophospholipid bilayers studied by ESR

      BIOPHYSICAL CHEMISTRY
    72. Linck, LM; Hayflick, SJ; Lin, DS; Battaile, KP; Ginat, S; Burlingame, T; Gibson, KM; Honda, M; Honda, A; Salen, G; Tint, GS; Connor, WE; Steiner, RD
      Fetal demise with Smith-Lemli-Opitz syndrome confirmed by tissue sterol analysis and the absence of measurable 7-dehydrocholesterol Delta(7)-reductase activity in chorionic villi

      PRENATAL DIAGNOSIS
    73. Sahir, N; Bahi, N; Evrard, P; Gressens, P
      Caffeine induces in vivo premature appearance of telencephalic vesicles

      DEVELOPMENTAL BRAIN RESEARCH
    74. Nowaczyk, MJM; Heshka, T; Kratz, LE; Kelley, RE
      Difficult prenatal diagnosis in mild Smith-Lemli-Opitz syndrome

      AMERICAN JOURNAL OF MEDICAL GENETICS
    75. Loffler, J; Trojovsky, A; Casati, B; Kroisel, PM; Utermann, G
      Homozygosity for the W151X stop mutation in the Delta 7-sterol reductase gene (DHCR7) causing a lethal form of Smith-Lemli-Opitz syndrome: Retrospective molecular diagnosis

      AMERICAN JOURNAL OF MEDICAL GENETICS
    76. Krakowiak, PA; Nwokoro, NA; Wassif, CA; Battaile, KP; Nowaczyk, MJM; Connor, WE; Maslen, C; Steiner, RD; Porter, FD
      Mutation analysis and description of sixteen RSH/Smith-Lemli-Opitz syndrome patients: Polymerase chain reaction-based assays to simplify genotyping

      AMERICAN JOURNAL OF MEDICAL GENETICS
    77. Bacino, CA; Stockton, DW; Sierra, RA; Heilstedt, HA; Lewandowski, R; Van den Veyver, IB
      Terminal osseous dysplasia and pigmentary defects: Clinical characterization of a novel male lethal X-linked syndrome

      AMERICAN JOURNAL OF MEDICAL GENETICS
    78. Linck, LM; Lin, DS; Flavell, D; Connor, WE; Steiner, RD
      Cholesterol supplementation with egg yolk increases plasma cholesterol anddecreases plasma 7-dehydrocholesterol in Smith-Lemli-Opitz syndrome

      AMERICAN JOURNAL OF MEDICAL GENETICS
    79. Patrono, C; Rizzo, C; Tessa, A; Giannotti, A; Borrelli, P; Carrozzo, R; Piemonte, F; Bertini, E; Dionisi-Vici, C; Santorelli, FM
      Novel 7-DHCR mutation in a child with Smith-Lemli-Opitz syndrome

      AMERICAN JOURNAL OF MEDICAL GENETICS
    80. Grange, DK; Kratz, LE; Braverman, NE; Kelley, RI
      CHILD syndrome caused by deficiency of 3 beta-hydroxysteroid-Delta(8), Delta(7)-isomerase

      AMERICAN JOURNAL OF MEDICAL GENETICS
    81. Opitz, JM
      Behold the CHILD

      AMERICAN JOURNAL OF MEDICAL GENETICS
    82. Konig, A; Happle, R; Bornholdt, D; Engel, H; Grzeschik, KH
      Mutations in the NSDHL gene, encoding a 3 beta-hydroxysteroid dehydrogenase, cause CHILD syndrome

      AMERICAN JOURNAL OF MEDICAL GENETICS
    83. Yu, HW; Tint, GS; Salen, G; Patel, SB
      Detection of a common mutation in the RSH or Smith-Lemli-Opitz syndrome bya PCR-RFLP assay: IVS8-1G -> C is found in over sixty percent of US propositi

      AMERICAN JOURNAL OF MEDICAL GENETICS
    84. Ness, GC; Chambers, CM
      Feedback and hormonal regulation of hepatic 3-hydroxy-3-methylglutaryl coenzyme A reductase: The concept of cholesterol buffering capacity

      PROCEEDINGS OF THE SOCIETY FOR EXPERIMENTAL BIOLOGY AND MEDICINE
    85. Willner, JP
      Genetic evaluation and counseling in head and neck syndromes

      OTOLARYNGOLOGIC CLINICS OF NORTH AMERICA
    86. Fliesler, SJ; Richards, MJ; Miller, CY; Cenedella, RJ
      Cholesterol synthesis in the vertebrate retina: Effects of U18666A on rat retinal structure, photoreceptor membrane assembly, and sterol metabolism and composition

      LIPIDS
    87. Danzer, E; Schier, F; Giggel, S; Bondartschuk, M
      Smith-Lemli-Opitz syndrome: Case report and literature review

      JOURNAL OF PEDIATRIC SURGERY
    88. Kelley, RI; Hennekam, RCM
      The Smith-Lemli-Opitz syndrome

      JOURNAL OF MEDICAL GENETICS
    89. Jira, PE; Wevers, RA; de Jong, J; Rubio-Gozalbo, E; Janssen-Zijlstra, FSM; van Heyst, AFJ; Sengers, RCA; Smeitink, JAM
      Simvastatin: a new therapeutic approach for Smith-Lemli-Opitz syndrome

      JOURNAL OF LIPID RESEARCH
    90. McConihay, JA; Honkomp, AM; Granholm, NA; Woollett, LA
      Maternal high density lipoproteins affect fetal mass and extra-embryonic fetal tissue sterol metabolism in the mouse

      JOURNAL OF LIPID RESEARCH
    91. Incardona, JP; Gaffield, W; Lange, Y; Cooney, A; Pentchev, PG; Liu, S; Watson, JA; Kapur, RP; Roelink, H
      Cyclopamine inhibition of sonic hedgehog signal transduction is not mediated through effects on cholesterol transport

      DEVELOPMENTAL BIOLOGY
    92. Rizzo, C; Dionisi-Vici, C; D'Ippoliti, M; Fina, F; Sabetta, G; Federici, G
      A simple and rapid HPLC method for simultaneous determination of plasma 7-dehydrocholesterol and vitamin E: its application in Smith-Lemli-Opitz patients

      CLINICA CHIMICA ACTA
    93. Starck, L; Lovgren, A
      Diagnosis of Smith-Lemli-Opitz syndrome from stored filter paper blood specimens

      ARCHIVES OF DISEASE IN CHILDHOOD
    94. Nishino, H; Ishibashi, T
      Evidence for requirement of NADPH-cytochrome P450 oxidoreductase in the microsomal NADPH-sterol Delta 7-reductase system

      ARCHIVES OF BIOCHEMISTRY AND BIOPHYSICS
    95. Villavicencio, EH; Walterhouse, DO; Iannaccone, PM
      The Sonic hedgehog-Patched-Gli pathway in human development and disease

      AMERICAN JOURNAL OF HUMAN GENETICS
    96. Roux, C; Wolf, C; Mulliez, N; Gaoua, W; Cormier, V; Chevy, F; Citadelle, D
      Role of cholesterol in embryonic development

      AMERICAN JOURNAL OF CLINICAL NUTRITION
    97. Scriver, CR; Treacy, EP
      Is there treatment for "genetic" disease?

      MOLECULAR GENETICS AND METABOLISM
    98. Wallis, DE; Muenke, M
      Molecular mechanisms of holoprosencephaly

      MOLECULAR GENETICS AND METABOLISM
    99. Derry, JMJ; Gormally, E; Means, GD; Zhao, W; Meindl, A; Kelley, RI; Boyd, Y; Herman, GE
      Mutations in a Delta(8)-Delta(7) sterol isomerase in the tattered mouse and X-linked dominant chondrodysplasia punctata

      NATURE GENETICS
    100. Braverman, N; Lin, P; Moebius, FF; Obie, C; Moser, A; Glossmann, H; Wilcox, WR; Rimoin, DL; Smith, M; Kratz, L; Kelley, RI; Valle, D
      Mutations in the gene encoding 3 beta-hydroxysteroid-Delta(8),Delta(7)-isomerase cause X-linked dominant Conradi-Hunermann syndrome

      NATURE GENETICS


ASDD Area Sistemi Dipartimentali e Documentali, Università di Bologna, Catalogo delle riviste ed altri periodici
Documento generato il 15/08/20 alle ore 17:01:44