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La ricerca find articoli where soggetti phrase all words 'PRENATAL-DIAGNOSIS' sort by level,fasc_key/DESCEND, pagina_ini_num/ASCEND ha restituito 4154 riferimenti
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    1. Messineo, A; Fusaro, F; Mognato, G; Sabatti, M; D'Amore, ESG; Guglielmi, M
      Lung volume reduction surgery in lieu of pneumonectomy in an infant with severe unilateral pulmonary interstitial emphysema

      PEDIATRIC PULMONOLOGY
    2. Beeri, M; Haramati, Z; Rein, JJTA; Nir, A
      Parental knowledge and views of pediatric congenital heart disease

      ISRAEL MEDICAL ASSOCIATION JOURNAL
    3. Keegan, CE; Killeen, AA
      An overview of molecular diagnosis of steroid 21-hydroxylase deficiency

      JOURNAL OF MOLECULAR DIAGNOSTICS
    4. Tarantal, AF; O'Rourke, JP; Case, SS; Newbound, GC; Li, J; Lee, CI; Baskin, CR; Kohn, DB; Bunnell, RA
      Rhesus monkey model for fetal gene transfer: Studies with retroviral-basedvector systems

      MOLECULAR THERAPY
    5. Allen, VM; Windrim, R; Barrett, J; Ohlsson, A
      Management of monoamniotic twin pregnancies: a case series and systematic review of the literature

      BRITISH JOURNAL OF OBSTETRICS AND GYNAECOLOGY
    6. Whitby, E; Paley, MN; Davies, N; Sprigg, A; Griffiths, PD
      Ultrafast magnetic resonance imaging of central nervous system abnormalities in utero in the second and third trimester of pregnancy: comparison withultrasound

      BRITISH JOURNAL OF OBSTETRICS AND GYNAECOLOGY
    7. Gardiner, HM
      Successes and shortcomings of fetal echocardiography

      HOSPITAL MEDICINE
    8. Torricelli, F; Pescucci, C
      Isolation of fetal cells from the maternal circulation: Prospects for the non-invasive prenatal diagnosis

      CLINICAL CHEMISTRY AND LABORATORY MEDICINE
    9. Tredano, M; de Blic, J; Griese, M; Fournet, JC; Elion, J; Bahuau, M
      Clinical biological and genetic heterogeneity of the inborn errors of pulmonary surfactant metabolism

      CLINICAL CHEMISTRY AND LABORATORY MEDICINE
    10. Adinolfi, M; Sherlock, J
      Fetal cells in transcervical samples at an early stage of gestation

      JOURNAL OF HUMAN GENETICS
    11. Zhong, XY; Holzgreve, W; Hahn, S
      Risk free simultaneous prenatal identification of fetal Rhesus D status and sex by multiplex real-time PCR using cell free fetal DNA in maternal plasma

      SWISS MEDICAL WEEKLY
    12. Vial, Y; Tran, C; Addor, MC; Hohlfeld, P
      Screening for foetal malformations: performance of routine ultrasonographyin the population of the Swiss Canton of Vaud

      SWISS MEDICAL WEEKLY
    13. Rashed, MS
      Clinical applications of tandem mass spectrometry: ten years of diagnosis and screening for inherited metabolic diseases

      JOURNAL OF CHROMATOGRAPHY B
    14. Grangeot-Keros, L; Cointe, D
      Diagnosis and prognostic markers of HCMV infection

      JOURNAL OF CLINICAL VIROLOGY
    15. Gouarin, S; Palmer, P; Cointe, D; Rogez, S; Vabret, A; Rozenberg, F; Denis, F; Freymuth, F; Lebon, P; Grangeot-Keros, L
      Congenital HCMV infection: a collaborative and comparative study of virus detection in amniotic fluid by culture and by PCR

      JOURNAL OF CLINICAL VIROLOGY
    16. Eftedal, I; Schwartz, M; Bendtsen, H; Andersen, AN; Ziebe, S
      Single intragenic microsatellite preimplantation genetic diagnosis for cystic fibrosis provides positive allele identification of all CFTR genotypes for informative couples

      MOLECULAR HUMAN REPRODUCTION
    17. Cirigliano, V; Ejarque, M; Canadas, MP; Lloveras, E; Plaja, A; Perez, MD; Fuster, C; Egozcue, J
      Clinical application of multiplex quantitative fluorescent polymerase chain reaction (QF-PCR) for the rapid prenatal detection of common chromosome aneuploidies

      MOLECULAR HUMAN REPRODUCTION
    18. Sahinoglu, Z; Uludogan, M; Gurbuz, A; Kol, E
      Prenatal detection of fetal anomalies by ultrasonography in the second trimester: Our first results from Turkey

      PRENATAL AND NEONATAL MEDICINE
    19. Panagopoulos, P; Kanellopoulos, N; Deligeoroglou, E; Economou, A; Botsis, D
      Prenatal diagnosis of congenital bladder diverticulum

      PRENATAL AND NEONATAL MEDICINE
    20. Huggon, IC
      Practical guide to fetal echocardiography

      PRENATAL AND NEONATAL MEDICINE
    21. Gardiner, HM
      Fetal echo cardiography: 20 years of progress

      HEART
    22. Acquila, M; Bottini, F; Valetto, A; Caprino, D; Mori, PG; Bicocchi, MP
      A new strategy for prenatal diagnosis in a sporadic haemophilia B family

      HAEMOPHILIA
    23. Klein, I; Andrikovics, H; Bors, A; Nemes, L; Tordai, A; Varadi, A
      A haemophilia A and B molecular genetic diagnostic programme in Hungary: ahighly informative and cost-effective strategy

      HAEMOPHILIA
    24. Oranwiroon, S; Akkarapatumwong, V; Pung-Amritt, P; Treesucon, A; Veerakul, G; Mahasandana, C; Panyim, S; Yenchitsomanus, P
      Determination of haemophilia A carrier status by mutation analysis

      HAEMOPHILIA
    25. Lo, YMD
      Fetal DNA in maternal plasma: application to noninvasive blood group genotyping of the fetus

      TRANSFUSION CLINIQUE ET BIOLOGIQUE
    26. Kupferschmidt, O; Kruger, D; Held, TK; Ellerbrok, H; Siegert, W; Janitschke, K
      Quantitative detection of Toxoplasma gondii DNA in human body fluids by TaqMan polymerase chain reaction

      CLINICAL MICROBIOLOGY AND INFECTION
    27. Davies, SC; Oni, L
      Sickle cell disease screening programs - Integration into managed care

      DISEASE MANAGEMENT & HEALTH OUTCOMES
    28. Palau, F
      Friedreich's ataxia and frataxin: Molecular genetics, evolution and pathogenesis (Review)

      INTERNATIONAL JOURNAL OF MOLECULAR MEDICINE
    29. Crawford, DC; Acuna, JM; Sherman, SL
      FMR1 and the fragile X syndrome: Human genome epidemiology review

      GENETICS IN MEDICINE
    30. Zamerowski, ST; Lumley, MA; Arreola, RA; Dukes, K; Sullivan, L
      Favorable attitudes toward testing for chromosomal abnormalities via analysis of fetal cells in maternal blood

      GENETICS IN MEDICINE
    31. Driscoll, DA
      Prenatal diagnosis of the 22q11.2 deletion syndrome

      GENETICS IN MEDICINE
    32. Manji, S; Roberson, JR; Wiktor, A; Vats, S; Rush, P; Diment, S; Van Dyke, DL
      Prenatal diagnosis of 22q11.2 deletion when ultrasound examination revealsa heart defect

      GENETICS IN MEDICINE
    33. Applegarth, DA; Toone, JR
      Nonketotic hyperglycinemia (glycine encephalopathy): Laboratory diagnosis

      MOLECULAR GENETICS AND METABOLISM
    34. Bach, G
      Mucolipidosis type IV

      MOLECULAR GENETICS AND METABOLISM
    35. Yang, BZ; Mallory, JM; Roe, DS; Brivet, M; Strobel, GD; Jones, KM; Ding, JH; Roe, CR
      Carnitine/acylcarnitine translocase deficiency (neonatal phenotype): Successful prenatal and postmortem diagnosis associated with a novel mutation ina single family

      MOLECULAR GENETICS AND METABOLISM
    36. Hahn, S; Cho, K; Ryu, K; Kim, J; Pai, K; Kim, M; Park, H; Yoo, O
      Identification of four novel mutations in classical menkes disease and successful prenatal DNA diagnosis

      MOLECULAR GENETICS AND METABOLISM
    37. Toone, JR; Applegarth, DA; Coulter-Mackie, MB; James, ER
      Recurrent mutations in P- and T-proteins of the glycine cleavage complex and a novel T-protein mutation (N1451): A strategy for the molecular investigation of patients with nonketotic hyperglycinemia (NKH)

      MOLECULAR GENETICS AND METABOLISM
    38. Hogema, BM; Akaboshi, S; Taylor, M; Salomons, GS; Jakobs, C; Schutgens, RB; Wilcken, B; Worthington, S; Maropoulos, G; Grompe, M; Gibson, KM
      Prenatal diagnosis of succinic semialdehyde dehydrogenase deficiency: Increased accuracy employing DNA, enzyme, and metabolite analyses

      MOLECULAR GENETICS AND METABOLISM
    39. Miyazaki, Y; Ichikawa, I
      Role of the angiotensin receptor in the development of the mammalian kidney and urinary tract

      COMPARATIVE BIOCHEMISTRY AND PHYSIOLOGY A-MOLECULAR AND INTEGRATIVE PHYSIOLOGY
    40. Bendon, RW
      Review of some causes of stillbirth

      PEDIATRIC AND DEVELOPMENTAL PATHOLOGY
    41. Daikha-Dahmane, F; Dommergues, M; Narcy, F; Gubler, MC; Dumez, Y; Gauthier, E; Nordmann, Y; Nessmann, C; Terrasse, G; Muller, F
      Congenital erythropoietic porphyria: Prenatal diagnosis and autopsy findings in two sibling fetuses

      PEDIATRIC AND DEVELOPMENTAL PATHOLOGY
    42. Tan, KL; Tan, JAMA; Wong, YC; Wee, YC; Thong, MK; Yap, SF
      Combine-ARMS: A rapid and cost-effective protocol for molecular characterization of beta-thalassemia in Malaysia

      GENETIC TESTING
    43. Yang, YP; Corley, N; Garcia-Heras, J
      Reverse dot-blot hybridization as an improved tool for the molecular diagnosis of point mutations in congenital adrenal hyperplasia caused by 21-hydroxylase deficiency

      MOLECULAR DIAGNOSIS
    44. Roizen, NJ
      Down syndrome: Progress in research

      MENTAL RETARDATION AND DEVELOPMENTAL DISABILITIES RESEARCH REVIEWS
    45. Stockman, JA; de Alarcon, PA
      Overview of the state of the art of Rh disease: History, current clinical management, and recent progress

      JOURNAL OF PEDIATRIC HEMATOLOGY ONCOLOGY
    46. Lazzarotto, T; Galli, C; Pulvirenti, R; Rescaldani, R; Vezzo, R; La Gioia, A; Martinelli, C; La Rocca, S; Agresti, G; Grillner, L; Nordin, M; van Ranst, M; Combs, B; Maine, GT; Landini, MP
      Evaluation of the Abbott AxSYM cytomegalovirus (CMV) immunoglobulin M (IgM) assay in conjunction with other CMV IgM tests and a CMV IgG avidity assay

      CLINICAL AND DIAGNOSTIC LABORATORY IMMUNOLOGY
    47. Coata, G; Tilesi, F; Fizzotti, M; Lauro, V; Pennacchi, L; Tabilio, A; Di Renzo, GC
      Prenatal diagnosis of genetic abnormalities using fetal CD34(+) stem cellsin maternal circulation and evidence they do not affect diagnosis in laterpregnancies

      STEM CELLS
    48. Brookes, A
      Women's voices: Prenatal diagnosis and care for the disabled

      HEALTH CARE ANALYSIS
    49. Kemp, S; Pujol, A; Waterham, HR; van Geel, BM; Boehm, CD; Raymond, GV; Cutting, GR; Wanders, RJA; Hugo, HW
      ABCD1 mutations and the X-linked adrenoleukodystrophy mutation database: Role in diagnosis and clinical correlations

      HUMAN MUTATION
    50. Rossi, A; Superti-Furga, A
      Mutations in the diastrophic dysplasia sulfate transporter (DTDST) gene (SLC26A2): 22 Novel mutations, mutation review, associated skeletal phenotypes, and diagnostic relevance

      HUMAN MUTATION
    51. Strauss, RP
      "Only skin deep": Health, resilience, and craniofacial care

      CLEFT PALATE-CRANIOFACIAL JOURNAL
    52. Lebo, RV; Maher, T; Farrer, L; Fenerci, EY; Milunsky, JM
      Highly polymorphic short tandem repeat analyses clarify complex molecular test results

      DIAGNOSTIC MOLECULAR PATHOLOGY
    53. Crowe, DA; Allan, LD
      Patterns of pulmonary venous flow in the fetus with disease of the left heart

      CARDIOLOGY IN THE YOUNG
    54. Wilson, RC; Nimkarn, S; New, MI
      Apparent mineralocorticoid excess

      TRENDS IN ENDOCRINOLOGY AND METABOLISM
    55. Bilardo, CM; Muller, MA; Pajkrt, E
      Outcome of fetuses with increased nuchal translucency

      CURRENT OPINION IN OBSTETRICS & GYNECOLOGY
    56. Michailidis, GD; Economides, DL; Schild, RL
      The role of three-dimensional ultrasound in obstetrics

      CURRENT OPINION IN OBSTETRICS & GYNECOLOGY
    57. Trincado, DE; Rawlinson, WD
      Congenital and perinatal infections with cytomegalovirus

      JOURNAL OF PAEDIATRICS AND CHILD HEALTH
    58. McGaughran, J; Souter, DJ; Kuschel, CA
      Alveolar capillary dysplasia with antenatal anomalies mimicking trisomy 21

      JOURNAL OF PAEDIATRICS AND CHILD HEALTH
    59. Musfeld, DA; Buhler, EM; Heinzl, S
      Roberts-SC phocomelia syndrome

      GYNAKOLOGISCH-GEBURTSHILFLICHE RUNDSCHAU
    60. Niemimaa, M; Suonpaa, M; Perheentupa, A; Seppala, M; Heinonen, S; Laitinen, P; Ruokonen, A; Ryynanen, M
      Evaluation of first trimester maternal serum and ultrasound screening for Down's syndrome in Eastern and Northern Finland

      EUROPEAN JOURNAL OF HUMAN GENETICS
    61. Schuring-Blom, GH; Boer, K; Leschot, NJ
      A placental diploid cell line is not essential for ongoing trisomy 13 or 18 pregnancies

      EUROPEAN JOURNAL OF HUMAN GENETICS
    62. Verloes, A; Gillerot, Y; Van Maldergem, L; Schoos, R; Herens, C; Jamar, M; Dideberg, V; Lesenfants, S; Koulischer, L
      Major decrease in the incidence of trisomy21 at birth in south Belgium: mass impact of triple test?

      EUROPEAN JOURNAL OF HUMAN GENETICS
    63. Witters, I; Moerman, P; Van Assche, FA; Fryns, JP
      Cystic hygroma colli as the first echographic sign of the fetal akinesia sequence

      GENETIC COUNSELING
    64. Douglas, L; Wilson, RD
      Prenatally diagnosed microcephaly: A review of etiologies

      FETAL DIAGNOSIS AND THERAPY
    65. Scharf, A; Ghazwiny, MF; Steinborn, A; Baier, P; Sohn, C
      Evaluation of two-dimensional versus three-dimensional ultrasound in obstetric diagnostics: A prospective study

      FETAL DIAGNOSIS AND THERAPY
    66. Denis, D; Maugey-Laulom, B; Carles, D; Pedespan, JM; Brun, M; Chateil, JF
      Prenatal diagnosis of schizencephaly by fetal magnetic resonance imaging

      FETAL DIAGNOSIS AND THERAPY
    67. Greco, P; Vimercati, A; De Cosmo, L; Laforgia, N; Mautone, A; Selvaggi, L
      Mild ventriculomegaly as a counselling challenge

      FETAL DIAGNOSIS AND THERAPY
    68. Becker, R; Stiemer, B; Neumann, L; Entezami, M
      Mild ventriculomegaly, mild cerebellar hypoplasia and dysplastic choroid plexus as early prenatal signs of CHARGE association

      FETAL DIAGNOSIS AND THERAPY
    69. Carbillon, L; Seince, N; Largilliere, C; Bucourt, M; Uzan, M
      First-trimester diagnosis of sirenomelia - A case report

      FETAL DIAGNOSIS AND THERAPY
    70. Percin, EF; Guvenal, T; Cetin, A; Percin, S; Goze, F; Arici, S
      First-trimester diagnosis of Robinow syndrome

      FETAL DIAGNOSIS AND THERAPY
    71. Walsh, DS; Adzick, NS; Sutton, LN; Johnson, MP
      The rationale for in utero repair of myelomeningocele

      FETAL DIAGNOSIS AND THERAPY
    72. MacKenzie, TC; Guttenberg, ME; Nisenbaum, HL; Johnson, MP; Adzick, NS
      A fetal lung lesion consisting of bronchogenic cyst, bronchopulmonary sequestration, and congenital cystic adenomatoid malformation: The missing link?

      FETAL DIAGNOSIS AND THERAPY
    73. Babu, R; Kyle, P; Spicer, RD
      Prenatal sonographic features of congenital lobar emphysema

      FETAL DIAGNOSIS AND THERAPY
    74. Jenderny, J; Schmidt, W; Hecher, K; Hackeloer, BJ; Kerber, S; Kochhan, L; Held, KR
      Increased nuchal translucency, hydrops fetalis or hygroma colli - A new test strategy for early fetal aneuploidy detection

      FETAL DIAGNOSIS AND THERAPY
    75. Hosono, T; Chiba, Y; Shinto, M; Kandori, A; Tsukada, K
      A fetal Wolff-Parkinson-White syndrome diagnosed prenatally by magnetocardiography

      FETAL DIAGNOSIS AND THERAPY
    76. Cengiz, B; Baxi, L
      Congenital cataract in triplet pregnancy after IVF with frozen embryos: Prenatal diagnosis and management

      FETAL DIAGNOSIS AND THERAPY
    77. Theodoropoulou, M; Barta, C; Szoke, M; Guttman, A; Staub, M; Niederland, T; Solyom, J; Fekete, G; Sasvari-Szekely, M
      Prenatal diagnosis of steroid 21-hydroxylase deficiency by allele-specificamplification

      FETAL DIAGNOSIS AND THERAPY
    78. Kamata, S; Sawai, T; Usui, N; Nose, K; Kitayama, Y; Nakai, H; Okuyama, H; Okada, A; Kawaguchi, H; Chiba, Y
      Bilateral diaphragmatic hernia followed by fetal ultrasonography - A report of two cases

      FETAL DIAGNOSIS AND THERAPY
    79. Noomen, P; van den Berg, C; de Ruyter, JLM; Van Opstal, D; Los, FJ
      Prevalence of tetraploid metaphases in semidirect and cultured chorionic villi

      FETAL DIAGNOSIS AND THERAPY
    80. Golombeck, K; Jacobs, VR; von Kaisenberg, C; Oppermann, HC; Reinecke-Luthge, A; Weisner, D; Jonat, W
      Short rib-polydactyly syndrome type III: Comparison of ultrasound, radiology, and pathology findings

      FETAL DIAGNOSIS AND THERAPY
    81. Goodyear, PWA; Bannister, CM; Russell, S; Rimmer, S
      Outcome in prenatally diagnosed fetal agenesis of the corpus callosum

      FETAL DIAGNOSIS AND THERAPY
    82. Haak, MC; Cobben, JM; van Vugt, JMG
      First trimester diagnosis of split hand/foot by transvaginal ultrasound

      FETAL DIAGNOSIS AND THERAPY
    83. Bon, GG; Kenemans, P; Verstraeten, AA; Go, S; Philipi, PA; van Kamp, GJ; van Geijn, HP; van Vugt, JMG
      Maternal serum CA125 and CA15-3 antigen levels in normal and pathological pregnancy

      FETAL DIAGNOSIS AND THERAPY
    84. Roberts, D; Sweeney, E; Walkinshaw, S
      Congenital cystic adenomatoid malformation of the lung coexisting with recombinant chromosome 18 - A case report

      FETAL DIAGNOSIS AND THERAPY
    85. Sikovanyecz, J; Horvath, E; Sallay, E; Gellen, J; Pal, A; Szabo, J
      Fetomaternal transfusion and pregnancy outcome after cordocentesis

      FETAL DIAGNOSIS AND THERAPY
    86. Perrotin, F; Ayeva-Derman, M; Lardy, H; Cloarec, S; Lansac, J; Body, G
      Prenatal diagnosis and postnatal outcome of congenital megalourethra - Report of two cases

      FETAL DIAGNOSIS AND THERAPY
    87. Stipoljev, F; Latin, V; Kos, M; Miskovic, B; Kurjak, A
      Correlation of confined placental mosaicism with fetal intrauterine growthretardation - A case control study of placentas at delivery

      FETAL DIAGNOSIS AND THERAPY
    88. Mahieu-Caputo, D; Sonigo, P; Amiel, J; Simon, I; Aubry, MC; Lemerrer, M; Delezoide, AL; Gigarel, N; Dommergues, M; Dumez, Y
      Prenatal diagnosis of sporadic Apert syndrome: A sequential diagnostic approach combining three-dimensional computed tomography and molecular biology

      FETAL DIAGNOSIS AND THERAPY
    89. Hosono, T; Chiba, Y; Shinto, M; Miyashita, S; Muramaki, K; Kandori, A; Tsukada, K
      A case of fetal complete heart block recorded by magnetocardiography, ultrasonography and direct fetal electrocardiography

      FETAL DIAGNOSIS AND THERAPY
    90. Gruner, C; Kollert, A; Wildt, L; Dorr, HG; Beinder, E; Lang, N
      Intrauterine treatment of fetal goitrous hypothyroidism controlled by determination of thyroid-stimulating hormone in fetal serum - A case report andreview of the literature

      FETAL DIAGNOSIS AND THERAPY
    91. Hohmann, H; Michel, S; Reiber, W; Gunther, M; Claussen, U; von Eggeling, F
      Applicability of four new antibodies for the detection of fetal nucleated cells out of maternal blood by FISH analysis

      FETAL DIAGNOSIS AND THERAPY
    92. Park, SY; Kim, JW; Kim, YM; Kim, JM; Lee, MH; Lee, BY; Han, JY; Kim, MY; Yang, JH; Ryu, HM
      Frequencies of fetal chromosomal abnormalities at prenatal diagnosis: 10 years experiences in a single institution

      JOURNAL OF KOREAN MEDICAL SCIENCE
    93. Han, JY; Kim, KH; Park, JI; Kim, IH; Je, GH
      Detection of fetal erythroid cells from maternal blood using fluorescence in situ hybridization and liquid culture

      JOURNAL OF KOREAN MEDICAL SCIENCE
    94. Chaturvedi, LS; Srivastava, S; Mukherjee, M; Mittal, RD; Phadke, SR; Pradhan, S; Mittal, B
      Carrier detection in non-deletional Duchenne/Becker muscular dystrophy families using polymorphic dinucleotide (CA) repeat loci of dystrophin gene

      INDIAN JOURNAL OF MEDICAL RESEARCH
    95. Peckham, C; Tookey, P; Logan, S; Giaquinto, C
      Screening options for prevention of congenital cytomegalovirus infection

      JOURNAL OF MEDICAL SCREENING
    96. Berge, SJ; Plath, H; van de Vondel, PT; Appel, T; Niederhagen, B; Von Lindern, JJ; Reich, RH; Hansmann, M
      Fetal cleft lip and palate: sonographic diagnosis, chromosomal abnormalities, associated anomalies and postnatal outcome in 70 fetuses

      ULTRASOUND IN OBSTETRICS & GYNECOLOGY
    97. Cash, C; Set, P; Coleman, N
      The accuracy of antenatal ultrasound in the detection of facial clefts in a low-risk screening population

      ULTRASOUND IN OBSTETRICS & GYNECOLOGY
    98. Carroll, SGM; Lockyer, H; Andrews, H; Abdel-Fattah, S; McMillan, D; Kyle, PM; Soothill, PW
      Outcome of fetal talipes following in utero sonographic diagnosis

      ULTRASOUND IN OBSTETRICS & GYNECOLOGY
    99. Clementschitsch, G; Hasenohrl, G; Schaffer, H; Steiner, H
      Comparison between two- and three-dimensional ultrasound measurements of nuchal translucency

      ULTRASOUND IN OBSTETRICS & GYNECOLOGY
    100. Paul, C; Krampl, E; Skentou, C; Jurkovic, D; Nicolaides, KH
      Measurement of fetal nuchal translucency thickness by three-dimensional ultrasound

      ULTRASOUND IN OBSTETRICS & GYNECOLOGY


ASDD Area Sistemi Dipartimentali e Documentali, Università di Bologna, Catalogo delle riviste ed altri periodici
Documento generato il 31/05/20 alle ore 07:20:41