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La ricerca find articoli where soggetti phrase all words 'TURNER SYNDROME' sort by level,fasc_key/DESCEND, pagina_ini_num/ASCEND ha restituito 530 riferimenti
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    1. Kagan-Krieger, S
      Factors that affect coping with turner syndrome

      JOURNAL OF NURSING SCHOLARSHIP
    2. Zinn, AR; Ross, JL
      Molecular analysis of genes on Xp controlling turner syndrome and premature ovarian failure (POF)

      SEMINARS IN REPRODUCTIVE MEDICINE
    3. Leppig, KA; Disteche, CM
      Ring X and other structural X chromosome abnormalities: X inactivation andphenotype

      SEMINARS IN REPRODUCTIVE MEDICINE
    4. Lahn, BT; Pearson, NM; Jegalian, K
      The human Y chromosome, in the light of evolution

      NATURE REVIEWS GENETICS
    5. Uehara, S; Sato, K; Hashiyada, M; Obara, Y; Matsuzaki, S; Nata, M; Okamura, K
      X chromosome inactivation patterns in 45,X/46,XX mosaics

      JOURNAL OF HUMAN GENETICS
    6. Leneman, M; Buchanan, L; Rovet, J
      Where and what visuospatial processing in adolescents with congenital hypothyroidism

      JOURNAL OF THE INTERNATIONAL NEUROPSYCHOLOGICAL SOCIETY
    7. Abir, R; Fisch, B; Nahum, R; Orvieto, R; Nitke, S; Ben Rafael, Z
      Turner's syndrome and fertility: current status and possible putative prospects

      HUMAN REPRODUCTION UPDATE
    8. Bramswig, JH
      Long-term results of growth hormone therapy in Turner syndrome

      ENDOCRINE
    9. Perry, J; Palmer, S; Gabriel, A; Ashworth, A
      A short pseudoautosomal region in laboratory mice

      GENOME RESEARCH
    10. Zinn, AR
      The X chromosome and the ovary

      JOURNAL OF THE SOCIETY FOR GYNECOLOGIC INVESTIGATION
    11. Muscat, P; Lidov, M; Nahar, T; Tuhrim, S; Weinberger, J
      Vertebral artery dissection in Turner's syndrome: Diagnosis by magnetic resonance imaging

      JOURNAL OF NEUROIMAGING
    12. Calabrese, EJ
      Estrogen and related compounds: Biphasic dose responses

      CRITICAL REVIEWS IN TOXICOLOGY
    13. Naldi, L
      Turner's syndrome, melanocytic nevi and melanoma

      DERMATOLOGY
    14. Gibbs, P; Brady, BMR; Gonzalez, R; Robinson, WA
      Nevi and melanoma: Lessons from Turner's syndrome

      DERMATOLOGY
    15. Bagci, G; Acar, H; Tomruk, H
      Different chromosome Y abnormalities in Turner syndrome

      GENETIC COUNSELING
    16. Ogata, T; Onigata, K; Hotsubo, T; Matsuo, N; Rappold, G
      Growth hormone and gonadotropin-releasing hormone analog therapy in haploinsufficiency of SHOX

      ENDOCRINE JOURNAL
    17. Orliaguet, O; Pepin, JL; Bettega, G; Ferretti, G; Mignotte, HN; Levy, P
      Sleep apnoea and Turner's syndrome

      EUROPEAN RESPIRATORY JOURNAL
    18. Moldavsky, M; Lev, D; Lerman-Sagie, T
      Behavioral phenotypes of genetic syndromes: A reference guide for psychiatrists

      JOURNAL OF THE AMERICAN ACADEMY OF CHILD AND ADOLESCENT PSYCHIATRY
    19. Mumm, S; Herrera, L; Waeltz, PW; Scardovi, A; Nagaraja, R; Esposito, T; Schlessinger, D; Rocchi, M; Forabosco, A
      X/autosomal translocations in the Xq critical region associated with premature ovarian failure fall within and outside genes

      GENOMICS
    20. Uechi, T; Tanaka, T; Kenmochi, N
      A complete map of the human ribosomal protein genes: Assignment of 80 genes to the cytogenetic map and implications for human disorders

      GENOMICS
    21. Simon, JPA; Fabry, G
      Parsonage-Turner syndrome after total-hip arthroplasty

      JOURNAL OF ARTHROPLASTY
    22. Noordam, C; van der Burgt, I; Sengers, RCA; Delemarre-van de Waal, HA; Otten, BJ
      Growth hormone treatment in children with Noonan's syndrome: four year results of a partly controlled trial

      ACTA PAEDIATRICA
    23. Naeraa, RW; Gravholt, CH; Kastrup, KW; Svenstrup, B; Christiansen, JS
      Morning versus evening administration of estradiol to girls with Turner syndrome receiving growth hormone: impact on growth hormone and metabolism. Arandomized placebo-controlled crossover study

      ACTA PAEDIATRICA
    24. Harder, T; Kohlhoff, R; Dorner, G; Rohde, W; Plagemann, A
      Perinatal 'programming' of insulin resistance in childhood: critical impact of neonatal insulin and low birth weight in a risk population

      DIABETIC MEDICINE
    25. Bernasconi, S; Mariani, S; Falcinelli, C; Milioli, S; Iughetti, L; Forabosco, A
      SHOX gene in Leri-Weill syndrome and in idiopathic short stature

      JOURNAL OF ENDOCRINOLOGICAL INVESTIGATION
    26. Quintana-Murci, L; Krausz, C; McElreavey, K
      The human Y chromosome: function, evolution and disease

      FORENSIC SCIENCE INTERNATIONAL
    27. Stenberg, AE; Wang, H; Fish, J; Schrott-Fisher, A; Sahlin, L; Hultcrantz, M
      Estrogen receptors in the normal adult and developing human inner ear and in Turner's syndrome

      HEARING RESEARCH
    28. Grigelioniene, G; Schoumans, J; Neumeyer, L; Ivarsson, SA; Eklof, O; Enkvist, O; Tordai, P; Fosdal, I; Myhre, AG; Westphal, O; Nilsson, NO; Elfving, M; Ellis, I; Anderlid, BM; Fransson, I; Tapia-Paez, I; Nordenskjold, M; Hagenas, L; Dumanski, JP
      Analysis of short stature homeobox-containing gene (SHOX) and auxological phenotype in dyschondrosteosis and isolated Madelung deformity

      HUMAN GENETICS
    29. Giltay, JC; Ausems, MGEM; van Seumeren, I; Zewald, RA; Sinke, RJ; Faas, B; de Vroede, M
      Short stature as the only presenting feature in a patient with an isodicentric (Y)(q11.23) and gonadoblastoma. A clinical and molecular cytogenetic study

      EUROPEAN JOURNAL OF PEDIATRICS
    30. Lejarraga, H; Martinez, A; Rudaz, CG; Hauspie, R; Tibaldi, F; Keselman, A; Heinrich, J
      Height velocity in Argentinean girls with Turner's syndrome

      JOURNAL OF PEDIATRIC ENDOCRINOLOGY & METABOLISM
    31. Lebl, J; Pruhova, S; Zapletalova, J; Pechova, M
      IGF-I resistance and Turner's syndrome

      JOURNAL OF PEDIATRIC ENDOCRINOLOGY & METABOLISM
    32. Guarneri, MP; Abusrewil, SAS; Bernasconi, S; Bona, G; Cavallo, L; Cicognani, A; Di Battista, E; Salvatoni, A
      Turner's syndrome

      JOURNAL OF PEDIATRIC ENDOCRINOLOGY & METABOLISM
    33. Drop, SLS; Greggio, N; Cappa, M; Bernasconi, S
      Current concepts in tall stature and overgrowth syndromes

      JOURNAL OF PEDIATRIC ENDOCRINOLOGY & METABOLISM
    34. Binder, G; Fritsch, H; Schweizer, R; Ranke, MB
      Radiological signs of Leri-Weill dyschondrosteosis in Turner syndrome

      HORMONE RESEARCH
    35. Thomas, M; Massa, G; Bourguignon, JP; Craen, M; De Schepper, J; de Zegher, F; Dooms, L; Du Caju, M; Francois, I; Heinrichs, C; Malvaux, P; Rooman, R; Thiry-Counson, G; Vandeweghe, M; Maes, M
      Final height in children with idiopathic growth hormone deficiency treatedwith recombinant human growth hormone: The Belgian experience

      HORMONE RESEARCH
    36. Lebl, J; Zahradnikova, M; Vlasak, I; Neuhuber, F
      Discordant growth pattern and ovarian function in monozygotic twins with 45,X/46,XX mosaicism

      HORMONE RESEARCH
    37. Blaschke, RJ; Rappold, GA
      SHOX in short stature syndromes

      HORMONE RESEARCH
    38. Kim, JY; Rosenfeld, SR; Keyak, JH
      Increased prevalence of scoliosis in Turner syndrome

      JOURNAL OF PEDIATRIC ORTHOPAEDICS
    39. Wang, YH; McWilliam, SM; Barendse, W; Kata, SR; Womack, JE; Moore, SS; Lehnert, SA
      Mapping of 12 bovine ribosomal protein genes using a bovine radiation hybrid panel

      ANIMAL GENETICS
    40. Gravholt, CH; Frystyk, J; Flyvbjerg, A; Orskov, H; Christiansen, JS
      Reduced free IGF-I and increased IGFBP-3 proteolysis in Turner syndrome: modulation by female sex steroids

      AMERICAN JOURNAL OF PHYSIOLOGY-ENDOCRINOLOGY AND METABOLISM
    41. Boman, UW; Bryman, I; Halling, K; Moller, A
      Women with Turner syndrome: psychological well-being, self-rated health and social life

      JOURNAL OF PSYCHOSOMATIC OBSTETRICS AND GYNECOLOGY
    42. Uehara, S; Hanew, K; Harada, N; Yamamori, S; Nata, M; Niikawa, N; Okamura, K
      Isochromosome consisting of terminal short arm and proximal long arm X in a girl with short stature

      AMERICAN JOURNAL OF MEDICAL GENETICS
    43. Thomas, NS; Huson, SM
      Atypical phenotype in a female with a large Xp deletion

      AMERICAN JOURNAL OF MEDICAL GENETICS
    44. Keller, K; Williams, C; Seagle, B
      Klinefelter syndrome and cutis verticis gyrata

      AMERICAN JOURNAL OF MEDICAL GENETICS
    45. Wei, FL; Cheng, S; Badie, N; Elder, F; Scott, C; Nicholson, L; Ross, JL; Zinn, AR
      A man who inherited his SRY gene and Leri-Weill dyschondrosteosis from hismother and neurofibromatosis type 1 from his father

      AMERICAN JOURNAL OF MEDICAL GENETICS
    46. Mazzocco, MMM; Kelley, RI
      Preliminary evidence for a cognitive phenotype in Barth syndrome

      AMERICAN JOURNAL OF MEDICAL GENETICS
    47. Stankiewicz, P; Thiele, H; Giannakudis, I; Schlicker, M; Baldermann, C; Kruger, A; Dorr, S; Starke, H; Hansmann, I
      Kabuki syndrome-like features associated with a small ring chromosome X and XIST gene expression

      AMERICAN JOURNAL OF MEDICAL GENETICS
    48. Aviv, H; Heller, D; Fajardo, A; Hoot, A; Mavaro, L
      Sex chromosome mosaicism in gonads of a fetus with cystic hygroma and deletion of the short arm of Y chromosome including loss of SRY

      AMERICAN JOURNAL OF MEDICAL GENETICS
    49. Reinehr, T; Jauch, A; Zoll, B; Engel, U; Bartels, I; Andler, W
      Short stature in a mother and daughter caused by familial der(X)t(X;X)(p22.1-3;q26)

      AMERICAN JOURNAL OF MEDICAL GENETICS
    50. Stankiewicz, P; Helias-Rodzewicz, Z; Jakubow-Durska, K; Bocian, E; Obersztyn, E; Rappold, GA; Mazurczak, T
      Cytogenetic and molecular characterization of two isodicentric Y chromosomes

      AMERICAN JOURNAL OF MEDICAL GENETICS
    51. Digilio, MC; Marino, B; Toscano, A; Giannotti, A; Dallapiccola, B
      Congenital heart defects in Kabuki syndrome

      AMERICAN JOURNAL OF MEDICAL GENETICS
    52. Corballis, MC
      Is the handedness gene on the X chromosome? Comment on Jones and Martin (2000)

      PSYCHOLOGICAL REVIEW
    53. Morin, A; Guimarey, L; Apezteguia, M; Santucci, Z
      Effect of estrogen therapy on the growth of Turner Syndrome girls treated with growth hormone.

      MEDICINA-BUENOS AIRES
    54. Jolley, C; Langham, MR; Dillard, R; Novak, D
      Intraoperative endoscopy in a child with Turner's syndrome and gastrointestinal hemorrhage: A case report

      JOURNAL OF PEDIATRIC SURGERY
    55. Boucher, CA; Sargent, CA; Ogata, T; Affara, NA
      Breakpoint analysis of Turner patients with partial Xp deletions: implications for the lymphoedema gene location

      JOURNAL OF MEDICAL GENETICS
    56. Giannotti, A; Tiberio, G; Castro, M; Virgilii, F; Colistro, F; Ferretti, F; Digilio, MC; Gambarara, M; Dallapiccola, B
      Coeliac disease in Williams syndrome

      JOURNAL OF MEDICAL GENETICS
    57. Ogata, T; Matsuo, N; Nishimura, G
      SHOX haploinsufficiency and overdosage: impact of gonadal function status

      JOURNAL OF MEDICAL GENETICS
    58. Beck-Engeser, GB; Monach, PA; Mumberg, D; Yang, F; Wanderling, S; Schreiber, K; Espinosa, R; Le Beau, MM; Meredith, SC; Schreiber, H
      Point mutation in essential genes with loss or mutation of the second allele: Relevance to the retention of tumor-specific antigens

      JOURNAL OF EXPERIMENTAL MEDICINE
    59. Padero, C; Friedman, T; Salehian, B
      Comment on "Editorial: The role of androgens in women"

      JOURNAL OF CLINICAL ENDOCRINOLOGY AND METABOLISM
    60. Elgar, K; Campbell, R
      Annotation: The cognitive neuroscience of face recognition: Implications for developmental disorders

      JOURNAL OF CHILD PSYCHOLOGY AND PSYCHIATRY AND ALLIED DISCIPLINES
    61. Schwinger, E; Gembruch, U
      Intrauterine growth restriction. Some chromosomal, genetic and exogenic causes

      GYNAKOLOGE
    62. Cervantes, A; Guevara-Yanez, R; Lopez, M; Monroy, N; Aguinaga, M; Valdez, H; Sierra, C; Canun, S; Guizar, J; Navarrete, C; Zafra, G; Salamanca, F; Kofman-Alfaro, S
      PCR-PRINS-FISH analysis of structurally abnormal sex chromosomes in eight patients with Turner phenotype

      CLINICAL GENETICS
    63. Gray, BA; Bent-Williams, A; Wolff, DJ; Zori, RT
      A non-sex chromosome marker in a patient with an atypical Ullrich-Turner phenotype and mosaicism of 46,X,mar/46,XX

      CLINICAL GENETICS
    64. Krepischi-Santos, ACV; Carneiro, JDA; Svartman, M; Bendit, I; Odone, V; Vianna-Morgante, AM
      Deletion of the factor IX gene as a result of translocation t(X;1) in a girl affected by haemophilia B

      BRITISH JOURNAL OF HAEMATOLOGY
    65. Kirk, JMW; Betts, PR; Butler, GE; Donaldson, MDC; Dunger, DB; Johnston, DI; Kelnar, CJH; Price, DA; Wilton, P
      Short stature in Noonan syndrome: response to growth hormone therapy

      ARCHIVES OF DISEASE IN CHILDHOOD
    66. Johnston, DI; Betts, P; Dunger, D; Barnes, N; Swift, PGF; Buckler, JMH; Butler, GE
      A multicentre trial of recombinant growth hormone and low dose oestrogen in Turner syndrome: near final height analysis

      ARCHIVES OF DISEASE IN CHILDHOOD
    67. Paoloni-Giacobino, A; Lespinasse, J; Moix, I; Dahoun, SP
      A case of (X;15) translocation diagnosed as a paracentric inversion of Xp:diagnostic revision with FISH

      ANNALES DE GENETIQUE
    68. Musarella, MA; Verma, RS
      An infant with Turner-Down aneuploidy and massive capillary hemangioma of the orbit: a case report with review

      ANNALES DE GENETIQUE
    69. Bortolai, A; Melaragno, MI
      Cell-cycle kinetics of cell lines from patients with chromosomal mosaicism

      ANNALES DE GENETIQUE
    70. Hass, AD; Simmons, KE; Davenport, ML; Proffit, WR
      The effect of growth hormone on craniofacial growth and dental maturation in Turner syndrome

      ANGLE ORTHODONTIST
    71. Bione, S; Toniolo, D
      X chromosome genes and premature ovarian failure

      SEMINARS IN REPRODUCTIVE MEDICINE
    72. Murray, A
      Premature ovarian failure and the FMR1 gene

      SEMINARS IN REPRODUCTIVE MEDICINE
    73. Kenmochi, N; Yoshihama, M; Higa, S; Tanaka, T
      The human ribosomal protein L6 gene in a critical region for Noonan syndrome

      JOURNAL OF HUMAN GENETICS
    74. Dean, G; Nevin, NC; Mikkelsen, M; Karadima, G; Petersen, MB; Kelly, M; O'Sullivan, J
      Investigation of a cluster of children with Down's syndrome born to mothers who had attended a school in Dundalk, Ireland

      OCCUPATIONAL AND ENVIRONMENTAL MEDICINE
    75. MAZZANTI L; CAUDARELLA R; BERGAMASCHI R; BUFFA A; SCARANO E; PERRI A; MASI A; ZANZANI B; CACCIARI E
      Bone mineral metabolism in patients with Turner's syndrome treated with GH and estrogen: cross-sectional and longitudinal data

      Italian journal of mineral and electrolyte metabolism
    76. Clayton, PE; Cowell, CT
      Safety issues in children and adolescents during growth hormone therapy - a review

      GROWTH HORMONE & IGF RESEARCH
    77. Chrast, R; Scott, HS; Papasavvas, MP; Rossier, C; Antonarakis, ES; Barras, C; Davisson, MT; Schmidt, C; Estivill, X; Dierssen, M; Pritchard, M; Antonarakis, SE
      The mouse brain transcriptome by SAGE: Differences in gene expression between P30 brains of the partial trisomy 16 mouse model of Down syndrome (Ts65Dn) and normals

      GENOME RESEARCH
    78. Reiss, AL; Eliez, S; Schmitt, JE; Patwardhan, A; Haberecht, M
      Brain imaging in neurogenetic conditions: Realizing the potential of behavioral neurogenetics research

      MENTAL RETARDATION AND DEVELOPMENTAL DISABILITIES RESEARCH REVIEWS
    79. Mazzocco, MMM
      Advances in research on the fragile X syndrome

      MENTAL RETARDATION AND DEVELOPMENTAL DISABILITIES RESEARCH REVIEWS
    80. Geschwind, DH; Boone, KB; Miller, BL; Swerdloff, RS
      Neurobehavioral phenotype of Klinefelter syndrome

      MENTAL RETARDATION AND DEVELOPMENTAL DISABILITIES RESEARCH REVIEWS
    81. Ross, J; Zinn, A; McCauley, E
      Neurodevelopmental and psychosocial aspects of Turner syndrome

      MENTAL RETARDATION AND DEVELOPMENTAL DISABILITIES RESEARCH REVIEWS
    82. Cmejla, R; Blafkova, J; Stopka, T; Zavadil, J; Pospisilova, D; Mihal, V; Petrtylova, K; Jelinek, J
      Ribosomal protein S19 gene mutations in patients with Diamond-Blackfan anemia and identification of ribosomal protein S19 pseudogenes

      BLOOD CELLS MOLECULES AND DISEASES
    83. Lipman, TH; McKnight, HJ
      Children with chronic conditions: The importance of growth assessment

      NURSE PRACTITIONER FORUM-CURRENT TOPICS AND COMMUNICATIONS
    84. Attie, KM
      Genetic studies in idiopathic short stature

      CURRENT OPINION IN PEDIATRICS
    85. Mock, BA; Markert, UR; Vogelsang, H; Jager, L
      Selective T-cell deficiency in Turner's syndrome

      JOURNAL OF INVESTIGATIONAL ALLERGOLOGY & CLINICAL IMMUNOLOGY
    86. Moore, GE; Ruangvutilert, P; Chatzimeletiou, K; Bell, G; Chen, CK; Johnson, P; Harper, JC
      Examination of trisomy 13, 18 and 21 foetal tissues at different gestational ages using FISH

      EUROPEAN JOURNAL OF HUMAN GENETICS
    87. Schiller, S; Spranger, S; Schechinger, B; Fukami, M; Merker, S; Drop, SLS; Troger, J; Knoblauch, H; Kunze, J; Seidel, J; Rappold, GA
      Phenotypic variation and genetic heterogeneity in Leri-Weill syndrome

      EUROPEAN JOURNAL OF HUMAN GENETICS
    88. Giglio, S; Pirola, B; Arrigo, G; Dagrada, P; Bardoni, B; Bernardi, F; Russo, G; Argentiero, L; Forabosco, A; Carrozzo, R; Zuffardi, O
      Opposite deletions/duplications of the X chromosome: two novel reciprocal rearrangements

      EUROPEAN JOURNAL OF HUMAN GENETICS
    89. Gole, LA; Anandakumar, C; Yang, R; Chan, J; Wong, YC; Bongso, A
      Discrepancy between cytogenetic and FISH results on an amniotic fluid sample of 45,X/46,X,idic(Y)(p11)

      FETAL DIAGNOSIS AND THERAPY
    90. Siffroi, JP; Dupuy, O; Joye, N; Le Bourhis, C; Benzacken, B; Portnoi, MF; Berkane, N; Franco, JC; Studer, C; Carbonne, B; Gonzales, M; Bucourt, M; Uzan, S; Uzan, M; Milliez, J; Wolf, JP; Taillemite, JL; Dadoune, JP
      Usefulness of fluorescence in situ hybridization for the diagnosis of turner mosaic fetuses with small ring X chromosomes

      FETAL DIAGNOSIS AND THERAPY
    91. Finsterer, J; Zartl, M; Samec, P
      Spontaneous cerebral haemorrhage without hypertension in non-mosaic 45X Turner's syndrome

      JOURNAL OF CLINICAL NEUROSCIENCE
    92. Rosati, P; Guariglia, L
      Prognostic value of ultrasound findings of fetal cystic hygroma detected in early pregnancy by transvaginal sonography

      ULTRASOUND IN OBSTETRICS & GYNECOLOGY
    93. Idilman, R; De Maria, N; Colantoni, A; Kugelmas, M; Van Thiel, DH
      Cirrhosis in Turner's syndrome: case report and literature review

      EUROPEAN JOURNAL OF GASTROENTEROLOGY & HEPATOLOGY
    94. Paoloni-Giacobino, A; Dahoun, SP; Sizonenko, PC; Stalberg, A; Chardonnens, D; Campana, A
      A case of 45,X Turner syndrome with spontaneous ovulation proven by ultrasonography

      GYNECOLOGICAL ENDOCRINOLOGY
    95. Tsuchiya, KD; Willard, HF
      Chromosomal domains and escape from X inactivation: comparative X inactivation analysis in mouse and human

      MAMMALIAN GENOME
    96. Fanos, V; Schena, S; Dal Moro, A; Portuese, A; Antoniazzi, F
      Multicystic kidney dysplasia and Turner syndrome: two cases and a literature review

      PEDIATRIC NEPHROLOGY
    97. Bilge, I; Kayserili, H; Emre, S; Nayir, A; Sirin, A; Tukel, T; Bas, F; Kilic, G; Basaran, S; Gunoz, H; Apak, M
      Frequency of renal malformations in Turner syndrome: analysis of 82 Turkish children

      PEDIATRIC NEPHROLOGY
    98. Chang, P; Tsai, WY; Hou, JW; Hsiao, PH; Lee, JS
      Autoimmune thyroiditis in children with Turner syndrome

      JOURNAL OF THE FORMOSAN MEDICAL ASSOCIATION
    99. Chang, P; Tsau, YK; Tsai, WY; Tsai, WS; Hou, JW; Hsiao, PH; Lee, JS
      Renal malformations in children with Turner's syndrome

      JOURNAL OF THE FORMOSAN MEDICAL ASSOCIATION
    100. Kawabata, G; Sato, M; Okamoto, Y; Mizuno, Y; Akematsu, T; Okada, H
      Laparoscopic removal of gonads in a Turner's syndrome mosaic female patient with isodicentric Y chromosome

      INTERNATIONAL JOURNAL OF UROLOGY


ASDD Area Sistemi Dipartimentali e Documentali, Università di Bologna, Catalogo delle riviste ed altri periodici
Documento generato il 22/01/21 alle ore 05:44:49