biomedicina slovenica


pr=Canki : 90

  1. Canki Nina
    Izvlečki 3. kongres genetikov Jugoslavije z mednarodno udeležbo; 1987 maj 31 - jun 4; Ljubljana
    [Abstracts of the 3rd Congress of Yugoslav geneticists with international participation; 1987 May 31 - Jun 4; Ljubljana]
    1987
  2. Canki-Klain Nina; Kovačić Sanja
    What's new in the diagnosis, treatment and prevention of cystic fibrosis? Programme and abstracts of the 1st eastern European CF conference; 2008 Nov 28-30; Zagreb
    2008
  3. Sršen Valentina; Koršič Marjan; Pečak F; Tršinar B; Tonin M; Kač-Vičar M; Kopač Š; Canki N
    Mielomeningokela
    1987
  4. Milič A; Piluso G; Ventriglia V; Damico F; Kovač B; Trlaja A; Mitrovič Z; Zurak N; Politano L; Canki-Klain N
    Mutation spectrum of CAPN3 gene in LGMD2A patients in Croatia
    2002
  5. Milič A; Kovač B; Leturcq F; Zurak N; Canki-Klain N
    High incidence of 550delA mutation in limb-girdle muscular dystrophy type 2A (LGMD2A) in Croatia
    2001
  6. Canki-Klain N
    The impact of molecular diagnosis on management and counselling in major inherited neuromuscular disorders
    2003
  7. Canki-Klain N; Milic A; Kovac B; Trlaja A; Grgicevic D; Zurak N; Feingold J
    Carrier frequency of 550delA mutation of CAPN3 gene in Croatia
    2002
  8. Stirn-Kranjc B; Canki-Klain N; Kaplan J
    Diagnostika Norrijeve bolezni
    1998
  9. Canki Nina; Rethore Marie odile
    Kromosomopatije in dermatoglifi
    1976
  10. Canki Nina; Debevec Marija; Rainer Srečko
    Pomen morfologije kromatid v klinični citogenetiki
    1975
  11. Canki Nina; Rainer Srečko
    Tip in protitip
    1976
  12. Canki N; Rainer S
    Pomen zgodnje amniocenteze pri določanju dednih bolezni
    1976
  13. Eržen M; Canki N; Zupan J; Talan T
    Multidisciplinarna diagnostika embrijske in fetalne patologije
    1984
  14. Canki N
    Etiologija intereseksualnih stanj s poudarkom na praktični pomen
    1984
  15. Eržen M; Canki N; Rainer S; Debevec M; Šinkovec J; Novak Ž; Cerar V
    Multidisciplinary diagnostic approach to embryonal and fetal pathology in preventing the birth of abnormal children
    1985
  16. Canki N; Rainer S; Debevec M
    Preprečevanje razvojnih nepravilnosti živčne cevi s pomočjo metod prenatalne diagnostike
    1985
  17. Canki N
    Maladie amniotique chez la mere et cardipathies graves chez deux enfants
    1985
  18. Eržen M; Canki N; Rainer S; Šinkovec J; Cerar V; Novak-Antolič Ž
    Značaj multidisciplinarne diagnostike embrijske i fetalne patologije u sprečavanju abnormalnog nasledstva
    1985
  19. Canki N; Bratanič B; Brezigar A; Brus L; Debevec M; Grošelj I; Rainer S
    Kromosomske anomalije kot povzročitelji ženske infertilnosti in sterilnosti
    1981
  20. Canki N; Grošelj I
    Važnost antenatalne dijagnostike u sprečavanju rođenja abnormalne djece
    1983
  21. Canki N
    Kromosomske anomalije kot povzročitelji subfertilnosti pri moškem
    1982
  22. Canki N
    Razvojne nepravilnosti živčane cijevi i genetsko savjetovanje
    1984
  23. Canki N; Rainer S
    Genetika, pravo i trudnoća
    1983
  24. Canki N; Tivadar I; Župančič N; Debevec M
    Citogenetska študija sedmih bolnic z ataksijo-teleangiektazijo
    1983
  25. Tivadar I; Canki N; Župančič N; Jeras J
    Ataksija - teleangiektazija
    1983
  26. Canki N; Tivadar I; Župančič N; Debevec M
    Kromosomske nepravilnosti u ataksiji-teleangiektaziji
    1983
  27. Canki N; Reiner Ž
    Teratogeno djelovanje antikonvulziva s posebnim osvrtom na fetalni hidantoinski sindrom
    1983
  28. Debevec M; Canki N
    PERICENTRIčNA INVERZIJA KROMOSOMA 9 PRI STERILNI žENI IN NJENI MATERI: INV(9) (P23Q31)
    1982
  29. Canki N; Boue J; Cerar V; Debevec M; Eržen M; Grošelj I; Istenič V; Lenart L; Meden H; Novak Ž; Rainer S
    ULOGA TIMSKOG RADA U SPREčAVANJU ROÐENJA NENORMALNE DJECE
    1982
  30. Canki N; Debevec M; Rainer S; Rethore MO
    DELNA MONOSOMIJA KRATKEGA KRAKA KROMOSOMA 9 ZARADI RECIPROčNE TRANSLOKACIJE PRI OčETU T (9;15) (P22;Q26) PAT
    1982
  31. Canki N; Brus L; Matajc L
    POSTUPAKPRI INTERSEKSUALNIM STANJIMA U NOVOROÐENAčKO DOBA
    1981
  32. Canki N
    OSNOVNA SPOZNANJA HUMANE GENETIKE
    1981
  33. Rainer S; Canki N; Debevec M
    IDENTIFICATION DES CHROMOSOMES ET LE CONSEIL GENETIQUE
    1980
  34. Rainer S; Canki N; Debevec M
    CHROMOSOMOPATHIES IN FAMILY PLANNING
    1980
  35. Canki N; Debevec M; Turk M; Avanzo-Velkavrh M
    TRISOMIJA 11Q USLIJED T (11; 14) (Q14;P12) MAS: PRIKAZ SLUčAJA
    1981
  36. Eržen M; Canki N; Vončina D
    CEREBRO-HEPATO-RENAL (ZELLWEGER'S) SYNDROME
    1980
  37. Debevec M; Canki N
    A PERICENTRIC INVERSION OF CHROMOSOME 9 IN STERILE WOMAN AND HER MOTHER: INV(9) (P23Q31)
    1980
  38. Canki N; Debevec M; Reš P
    FAMILIAL MALE STERILITY ASSOCIATED WITH REARRANGEMENTS OF CHROMOSOME STRUCTURE TRANSMITED BY MOTHER: 45,XX,-15,-20,-21,+T(15Q20Q),+T(20P21Q),INV(9)(P11Q1209)
    1980
  39. Canki N; Rainer S; Brus L; Debevec M; Matajc L
    MANAGEMENT OF PATIENTS WITH INTERSEX STATES
    1979
  40. Canki N
    UčINKI GENSKE KOLIčINE PRI ANOMALIJAH X KROMOSOMA
    1981
  41. Canki N; Boue J
    ZNAčENJE UPOTREBE KROMOSOMSKIH TEHNIKA PRUGA U ANTENATALNOJ DIJAGNOSTICI
    1980
  42. Canki N
    UčINCI KOLIčINE GENA KOD ANOMALIJA X-KROMOSOMA
    1980
  43. Canki N; Konjajev Z; Debevec M; Rainer S; Rethore M-O
    TRISOMIE 10Q24 - 10QTER TRANSLOCATION FAMILIALE T (10;14) (Q24;Q32)
    1980
  44. Canki N
    GENETSKO SVETOVANJE
    1979
  45. Cindro J; Fetih A; Kos L; Canki N
    HOLOACARDIUS ACEPHALUS. DIAGNOSTIčNI PROBLEM IN VODSTVO PORODA
    1979
  46. Canki N; Rainer S; Brus L; Debevec M; Matajc L
    MANAGEMENT OF PATIENTS WITH INTERSEX STATES
    1979
  47. Canki N; Debevec M; Rainer S; Reš P
    PARACENTRIC INVERSION (5) (Q21;Q32) IN MOTHER AND HER 47, XXY SON
    1978
  48. Canki N; Debevec M; Rainer S
    ULOGA KLINIčKE CITOGENETIKE U PEDIJATRIJI
    1978
  49. Canki N; Debevec M; Rainer S; Bravar D
    L'IMPORTANCE TECHNIQUES DE MARQUAGE CHROMOSOMIQUE EN DIAGNOSTIC PRENATAL A PROPOS D'UNE TRISOMIE 10P PAR T (10,21) (Q21 ; Q21) PAT
    1979
  50. Canki N; Dutrillaux B; Debevec M; Rainer S
    LES INVERSIONS PARACENTRIQUES ET LES ANOMALIES CHROMOSOMIQUES CONCOMITANTES. A PROPOS DE DEUX CAS: 45, X, INV (7) (Q11.3Q22.3) PAT, 47, XX, INV (5) (Q21Q32) MAT
    1978
  51. Canki N; Dutrillaux B; Tivadar I
    DYSTROPHIE MUSCULAIRE DE DUCHENNE CHEZ UNE PETITE FILLE PORTEUSE D'UNE TRANSLOCATION T(X;3) (P21;Q13) DE NOVO
    1979
  52. Eržen M; Canki N; Vončina D
    CEREBRO-HEPATO-RENALNI (ZELLWEGEROV) SINDROM: PATOANATOMSKA I GENETSKA ANALIZA SLUčAJA
    1979
  53. Canki N; Debevc M; Rainer S
    GENETSKO SAVJETOVANJE
    1978
  54. Canki N; Debevec M; Kenda S; Rainer S
    PRESENTATION D'UN CAS DE SYNDROME OCULO-CEREBRO-RENAL CHEZ UN NOUVEAU-NE
    1976
  55. Canki N; Debevec M; Rainer S; Rethore M-O
    TRISOMIE 4Q26 4QTER PAR TRANSLOCATION T(4;18) (Q26;Q23)MAT
    1977
  56. Stirn-Kranjc B; Canki-Klain N; Kaplan J
    Norriejeva bolezen
    1999
  57. Kazazan Haig H; Ravnik-Glavač Metka; Glavač Damjan; Komel Radovan; Ferec C; Canki-Klain N; Durie P; Rozen R; Morgan K; Fujiwara M
    Population variation of common cystic fibrosis mutations
    1994
  58. Veble A; Canki-Klain N; Debevec M; Gregorčič J; Meden-Vrtovec H; Tomaževič T
    Chromosomal analysis of early pregnancy losses in patients after in vitro fertilization
    1997
  59. Devoto M; Romeo G; ten Kate LP; Chevalier F; Bozon D; Estivill X; Casals T; Abeliovich D; Lerer I; Canki-Klain N; Ravnik-Glavač M
    No evidence for segregation distortion of cystic fibrosis alleles among sibs of cystic fibrosis patients
    1995
  60. Canki-Klain N
    Medical geneticist and abnormal fetus
    1994
  61. Battelino T; Kržišnik C; Canki-Klain N
    Prenatalna diagnostika in ukrepi pri motnjah diferenciacije spola
    1995
  62. Canki-Klain N
    Genetski vidiki diferenciacije spola
    1995
  63. Debevec M; Canki-Klain N; Brezigar A; Blejec T; Cerar V
    Abnormal pregnancy sonogram and chromosomal anomalies
    1992
  64. Warburton D; Byrne J; Canki N
    Chromosome anomalies and prenatal development: an atlas
    1991
  65. Mercier B; Lissens W; Novelli G; Kalaydjieva L; de Arce M; Kapranov N; Canki-Klain N; Estivill X; Palacio Ana; Cashman S
    A cluster of cystic fibrosis mutations in exon 17b of the CFTR gene: a site for rare mutations
    1994
  66. Canki-Klain N; Stanescu V; Bebler P; Maroteaux P
    Pseudodiastrophic dysplasia evolution with age and management. Report of two new cases and review of the literature
    1990
  67. Peterlin B; Canki-Klain N; Morela V; Stirn B; Rainer S; Cerar V
    Prevalence of retinitis pigmentosa in Slovenia
    1992
  68. Veble A; Canki-Klein N; Debevec M; Tomaževič T
    Chromosomal analysis of spontaneous abortions after in vitro fertilization (IVF)
    1992
  69. Mercier B; Lissens W; Novelli G; Kalaydjieva L; De Arce M; Kapranov N; Canki-Klain N; Lenoir G; Chauveau P; Lenaerts C; Rault G; Cashman S
    Identification of eight novel mutations in a collaborative analysis of a part of the second transmembrane domain of the CFTR gene
    1993
  70. Audrezet MP; Canki-Klain N; Mercier B; Bracar D; Verlingue C; Ferec C
    Identification of three novel mutations (457 TAT-->G, D192G, Q685X) in the Slovenian CF patients
    1994
  71. Canki-Klain N
    Cyclotocephaly: severe form of midline malformation association
    1993
  72. Debevec M; Canki-Klain N
    Prenatalna diagnostika kromosomskih anomalij v Sloveniji: analiza 1834 primerov
    [Prenatal diagnosis of chromosomal anomalies in Slovenia: an analysis of 1834 cases]
    1994
  73. Canki-Klain N; Stanescu V; Stanescu R; Šinkovec J; Debevec M; Maroteaux P
    Lethal short limb dwarfism with dysmorphic face, omphalocele and severe ossification defect: Piepkorn syndrome or severe "boomerang dysplasia"?
    1992
  74. Stern MH; Soulier J; Rosenzwajg M; Nakahara K; Canki-Klain N; Aurias A; Sigaux F; Kirsch IR
    MTCP-1: a novel gene on the human chromosome Xq28 translocated to the T cell receptor alpha/delta locus in mature T cell proliferations
    1993
  75. Canki-Klain N
    Genetsko svetovanje
    1993
  76. Prodan M; Canki-Klain N
    Diagnostika in zdravljenje genetskih bolezni
    1993
  77. Peterlin B; Zidar J; Meznarič-Petruša M; Canki-Klain N; Komel R; Boileau C; Župančič N
    Pristop k diagnostiki Duchennove in Beckerjeve mišične distrofije
    1992
  78. Ravnik-Glavač M; Gasparini P; Peterlin B; Štrukelj M; Glavač D; Canki-Klain N; Pignatti PF; Komel R
    Cystic fibrosis gene mutations and linked RFLPs in the Slovenian population
    1992
  79. Ravnik-Glavač M; Komel R; Peterlin B; Pignatti PF; Štrukelj M; Canki-Klain N; Cerar V; Debevec M
    Določanje informativnosti in prenatalna diagnostika cistične fibroze z metodo PCR
    [Determination of informativity and prenatal diagnosis of cystic fibrosis with PCR method]
    1992
  80. Kokalj-Vokač N; Canki-Klain N; Debevec M; Veble A
    46,XX,inv(10)(p14q22)mat pri ženski s spontanimi splavi
    [46,XX,inv(10)(p14q22)mat in a woman with spontaneous abortions]
    1992
  81. Canki N
    Genetika u reprodukciji
    1990
  82. Canki N
    3.kongres genetikov Jugoslavije z mednarodno udeležbo: izvlečki
    1987
  83. Canki-Klain N
    Principi genetskog savjetovanja s posebnim osvrtom na prenatalnu dijagnostiku
    1990
  84. Canki N; Debevec M; Blejec T; Cerar V; Rainer S; Grošelj I
    Uporaba horionskih resic v prenatalni diagnostiki
    1986
  85. Canki-Klain N; Cerar V
    Cistična fibroza in genetsko svetovanje
    [Cystic fibrosis and genetic counselling]
    1990
  86. Canki N
    Genetski vzroki neplodnosti pri ženski in moškem
    1989
  87. Canki N
    Genetski dejavniki v reprodukciji
    1989
  88. Brezigar A; Canki N; Debevec M; Cerar V; Završnik T; Malenšek B
    Detection of familial translocation t(4;8) (p153;p21) by ultrasound screening of malformed fetus
    1988
  89. Canki N; Warburton D; Byrne J
    Morphological characteristics of monosomy X in spontaneous abortions
    1988
  90. Eržen Mojca; Canki Nina; Rainer Srečko; Debevec Marija; Gubina Marija; Novak-Antolič Živa; Cerar Vasilij
    Pomen multidisciplinarne diagnostike embrijske in fetalne patologije pri preprečevanju abnormalnega potomstva
    [Role of multidisciplinary diagnostic approach to embryonal and fetal pathology in preventing the birth of abnormal children]
    1986


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