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1. 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
   
   G.H. Schuring-Blom et al., "A placental diploid cell line is not essential for ongoing trisomy 13 or 18 pregnancies", EUR J HUM G, 9(4), 2001, pp. 286-290
2. Schuring-Blom, GH; Hoovers, JMN; van Lith, JMM; Knegt, AD; Leschot, NJ
   FISH analysis of fetal nucleated red blood cells from CVS washings in cases of aneuploidy
   PRENATAL DIAGNOSIS
   
   G.H. Schuring-Blom et al., "FISH analysis of fetal nucleated red blood cells from CVS washings in cases of aneuploidy", PRENAT DIAG, 21(10), 2001, pp. 864-867
3. de Vries, JWA; Repping, S; Oates, R; Carson, R; Leschot, NJ; van der Veen, F
   Absence of deleted in azoospermia (DAZ) genes in spermatozoa of infertile men with somatic DAZ deletions
   FERTILITY AND STERILITY
   
   J.W.A. de Vries et al., "Absence of deleted in azoospermia (DAZ) genes in spermatozoa of infertile men with somatic DAZ deletions", FERT STERIL, 75(3), 2001, pp. 476-479
4. Goddijn, M; Leschot, NJ
   Genetic aspects of miscarriage
   BEST PRACTICE & RESEARCH IN CLINICAL OBSTETRICS & GYNAECOLOGY
   
   M. Goddijn e N.J. Leschot, "Genetic aspects of miscarriage", BEST P R CL, 14(5), 2000, pp. 855-865
5. Leschot, NJ
   Qigong: A personal experience
   ALTERNATIVE THERAPIES IN HEALTH AND MEDICINE
   
   N.J. Leschot, "Qigong: A personal experience", ALTERN TH H, 6(5), 2000, pp. 98-99
6. de Pater, JM; Schuring-Blom, GH; Nieste-Otter, MA; van Nesselrooij, B; Kapitein, B; Christiaens, GCML; Leschot, NJ
   Trisomy 8 in chorionic villi - unpredictable results in follow-up
   PRENATAL DIAGNOSIS
   
   J.M. de Pater et al., "Trisomy 8 in chorionic villi - unpredictable results in follow-up", PRENAT DIAG, 20(5), 2000, pp. 435-437
7. de Graaf, IM; Cuckle, HS; Pajkrt, E; Leschot, NJ; Bleker, OP; van Lith, JMM
   Co-variables in first trimester maternal serum screening
   PRENATAL DIAGNOSIS
   
   I.M. de Graaf et al., "Co-variables in first trimester maternal serum screening", PRENAT DIAG, 20(3), 2000, pp. 186-189
8. Mohrschladt, MF; Bijlsma, EK; Sluijter, S; De Coo, RFM; Hoovers, JMN; Leschot, NJ
   A patient with a de novo t(6;9) and an interstitial duplication of (9)(q21.2q22.1)
   CLINICAL DYSMORPHOLOGY
   
   M.F. Mohrschladt et al., "A patient with a de novo t(6;9) and an interstitial duplication of (9)(q21.2q22.1)", CLIN DYSMOR, 8(3), 1999, pp. 211-214
9. Hoogerwaard, EM; van der Wouw, PA; Wilde, AAM; Bakker, E; Ippel, PF; Oosterwijk, JC; Majoor-Krakauer, DF; van Essen, AJ; Leschot, NJ; de Visser, M
   Cardiac involvement in carriers of Duchenne and Becker muscular dystrophy
   NEUROMUSCULAR DISORDERS
   
   E.M. Hoogerwaard et al., "Cardiac involvement in carriers of Duchenne and Becker muscular dystrophy", NEUROMUSC D, 9(5), 1999, pp. 347-351
10. de Graaf, IM; Pajkrt, E; Keessen, M; Leschot, NJ; Bilardo, CM
    Enlarged nuchal translucency and low serum protein concentrations as possible markers for Zellweger syndrome
    ULTRASOUND IN OBSTETRICS & GYNECOLOGY
    
    I.M. de Graaf et al., "Enlarged nuchal translucency and low serum protein concentrations as possible markers for Zellweger syndrome", ULTRASOUN O, 13(4), 1999, pp. 268-270
11. de Graaf, IM; Jakobs, ME; Leschot, NJ; Ravkin, I; Goldbard, S; Hoovers, JMN
    Enrichment, identification and analysis of fetal cells from maternal blood: Evaluation of a prenatal diagnosis system
    PRENATAL DIAGNOSIS
    
    I.M. de Graaf et al., "Enrichment, identification and analysis of fetal cells from maternal blood: Evaluation of a prenatal diagnosis system", PRENAT DIAG, 19(7), 1999, pp. 648-652
12. de Graaf, IM; Pajkrt, E; Bilardo, CM; Leschot, NJ; Cuckle, HS; van Lith, JMM
    Early pregnancy screening for fetal aneuploidy with serum markers and nuchal translucency
    PRENATAL DIAGNOSIS
    
    I.M. de Graaf et al., "Early pregnancy screening for fetal aneuploidy with serum markers and nuchal translucency", PRENAT DIAG, 19(5), 1999, pp. 458-462
13. de Graaf, IM; van Bezouw, SMCA; Jakobs, ME; Leschot, NJ; Zondervan, HA; Bilardo, CM; Hoovers, JMN
    First-trimester non-invasive prenatal diagnosis of triploidy
    PRENATAL DIAGNOSIS
    
    I.M. de Graaf et al., "First-trimester non-invasive prenatal diagnosis of triploidy", PRENAT DIAG, 19(2), 1999, pp. 175-177
14. Hoogerwaard, EM; Bakker, E; Ippel, PF; Oosterwijk, JC; Majoor-Krakauer, DF; Leschot, NJ; Van Essen, AJ; Brunner, HG; van der Wouw, PA; Wilde, AAM; de Visser, M
    Signs and symptoms of Duchenne muscular dystrophy and Becker muscular dystrophy among carriers in the Netherlands: a cohort study
    LANCET
    
    E.M. Hoogerwaard et al., "Signs and symptoms of Duchenne muscular dystrophy and Becker muscular dystrophy among carriers in the Netherlands: a cohort study", LANCET, 353(9170), 1999, pp. 2116-2119
15. VANDERKOOI AJ; DEVISSER M; VANMEEGEN M; GINJAAR HB; VANESSEN AJ; JENNEKENS FGI; JONGEN PJH; LESCHOT NJ; BOLHUIS PA
    A NOVEL GAMMA-SARCOGLYCAN MUTATION CAUSING CHILDHOOD-ONSET, SLOWLY PROGRESSIVE LIMB-GIRDLE MUSCULAR-DYSTROPHY
    Neuromuscular disorders
    
    A.J. Vanderkooi et al., "A NOVEL GAMMA-SARCOGLYCAN MUTATION CAUSING CHILDHOOD-ONSET, SLOWLY PROGRESSIVE LIMB-GIRDLE MUSCULAR-DYSTROPHY", Neuromuscular disorders, 8(5), 1998, pp. 305-308
16. HANSSON K; POELMA WMJ; ZONDERVAN HA; LESCHOT NJ
    LOW-LEVEL MOSAICISM FOR BOTH TRISOMY-15 AND MONOSOMY-X IN AMNIOTIC-FLUID CELLS CONFIRMED IN FETAL TISSUES
    Prenatal diagnosis
    
    K. Hansson et al., "LOW-LEVEL MOSAICISM FOR BOTH TRISOMY-15 AND MONOSOMY-X IN AMNIOTIC-FLUID CELLS CONFIRMED IN FETAL TISSUES", Prenatal diagnosis, 18(9), 1998, pp. 975-978
17. LESCHOT NJ; VEJERSLEV LO
    PRENATAL-DIAGNOSIS IN EUROPE - PROCEEDINGS OF AN EUCROMIC WORKSHOP ONPRENATAL-DIAGNOSIS, PARIS, MAY 23-24, 1996
    European journal of human genetics
    
    N.J. Leschot e L.O. Vejerslev, "PRENATAL-DIAGNOSIS IN EUROPE - PROCEEDINGS OF AN EUCROMIC WORKSHOP ONPRENATAL-DIAGNOSIS, PARIS, MAY 23-24, 1996", European journal of human genetics, 5, 1997, pp. 1-6
18. LESCHOT NJ; KLOOSTERMAN MD
    PRENATAL-DIAGNOSIS IN THE NETHERLANDS
    European journal of human genetics
    
    N.J. Leschot e M.D. Kloosterman, "PRENATAL-DIAGNOSIS IN THE NETHERLANDS", European journal of human genetics, 5, 1997, pp. 51-56
19. MEUWISSEN RLJ; MEERTS I; HOOVERS JMN; LESCHOT NJ; HEYTING C
    HUMAN SYNAPTONEMAL COMPLEX PROTEIN-1 (SCP1) - ISOLATION AND CHARACTERIZATION OF THE CDNA AND CHROMOSOMAL LOCALIZATION OF THE GENE
    Genomics
    
    R.L.J. Meuwissen et al., "HUMAN SYNAPTONEMAL COMPLEX PROTEIN-1 (SCP1) - ISOLATION AND CHARACTERIZATION OF THE CDNA AND CHROMOSOMAL LOCALIZATION OF THE GENE", Genomics, 39(3), 1997, pp. 377-384
20. BLEIKER EMA; AARONSON NK; MENKO FH; HAHN DEE; VANASPEREN CJ; RUTGERS EJT; TENKATE LP; LESCHOT NJ
    GENETIC-COUNSELING FOR HEREDITARY CANCER - A PILOT-STUDY ON EXPERIENCES OF PATIENTS AND FAMILY MEMBERS
    Patient education and counseling
    
    E.M.A. Bleiker et al., "GENETIC-COUNSELING FOR HEREDITARY CANCER - A PILOT-STUDY ON EXPERIENCES OF PATIENTS AND FAMILY MEMBERS", Patient education and counseling, 32(1-2), 1997, pp. 107-116
21. DEPATER JM; SCHURINGBLOM GH; VANDENBOGAARD R; VANDERSIJSBOS CJM; CHRISTIAENS GCML; STOUTENBEEK P; LESCHOT NJ
    MATERNAL UNIPARENTAL DISOMY FOR CHROMOSOME-22 IN A CHILD WITH GENERALIZED MOSAICISM FOR TRISOMY-22
    Prenatal diagnosis
    
    J.M. Depater et al., "MATERNAL UNIPARENTAL DISOMY FOR CHROMOSOME-22 IN A CHILD WITH GENERALIZED MOSAICISM FOR TRISOMY-22", Prenatal diagnosis, 17(1), 1997, pp. 81-86
22. VANDERSIJSBOS CJM; STIGTER RH; CHRISTIAENS GCML; LESCHOT NJ
    PRENATAL AND POSTNATAL PREVALENCE OF TURNERS-SYNDROME - DATA PRESENTED WERE INSUFFICIENT TO CHALLENGE SPECIFICITY OF PRENATAL-DIAGNOSIS
    BMJ. British medical journal
    
    C.J.M. Vandersijsbos et al., "PRENATAL AND POSTNATAL PREVALENCE OF TURNERS-SYNDROME - DATA PRESENTED WERE INSUFFICIENT TO CHALLENGE SPECIFICITY OF PRENATAL-DIAGNOSIS", BMJ. British medical journal, 313(7048), 1996, pp. 47-47
23. LESCHOT NJ
    SPECIFIC APPROACHES TO FETAL CELLS ISOLATION FROM MATERNAL BLOOD - INTRODUCTION
    Early human development
    
    N.J. Leschot, "SPECIFIC APPROACHES TO FETAL CELLS ISOLATION FROM MATERNAL BLOOD - INTRODUCTION", Early human development, 47, 1996, pp. 69-72
24. GODDIJN M; VANDERVEEN F; SCHURINGBLOM GH; ANKUM WM; LESCHOT NJ
    CYTOGENETIC CHARACTERISTICS OF ECTOPIC PREGNANCY
    Human reproduction
    
    M. Goddijn et al., "CYTOGENETIC CHARACTERISTICS OF ECTOPIC PREGNANCY", Human reproduction, 11(12), 1996, pp. 2769-2771
25. LESCHOT NJ; SCHURINGBLOM GH; VANPROOIJENKNEGT AC; VERJAAL M; HANSSON K; WOLF H; KANHAI HHH; VANVUGT JMG; CHRISTIAENS GCML
    THE OUTCOME OF PREGNANCIES WITH CONFINED PLACENTAL CHROMOSOME MOSAICISM IN CYTOTROPHOBLAST CELLS
    Prenatal diagnosis
    
    N.J. Leschot et al., "THE OUTCOME OF PREGNANCIES WITH CONFINED PLACENTAL CHROMOSOME MOSAICISM IN CYTOTROPHOBLAST CELLS", Prenatal diagnosis, 16(8), 1996, pp. 705-712
26. VANLANGEN IM; OTTER MA; ARONSON DC; OVERWEGPLANDSOEN WCG; HENNEKAM RCM; LESCHOT NJ; HOOVERS JMN
    SUPERNUMERARY RING CHROMOSOME-20 CHARACTERIZED BY FLUORESCENCE IN-SITU HYBRIDIZATION
    Clinical genetics
    
    I.M. Vanlangen et al., "SUPERNUMERARY RING CHROMOSOME-20 CHARACTERIZED BY FLUORESCENCE IN-SITU HYBRIDIZATION", Clinical genetics, 49(1), 1996, pp. 49-53
27. LUNSHOF S; BOER K; LESCHOT NJ; POMP M; WOLF H
    PREGNANCY OUTCOME AFTER TRANSCERVICAL CVS WITH A FLEXIBLE BIOPSY FORCEPS - EVALUATION OF RISK-FACTORS
    Prenatal diagnosis
    
    S. Lunshof et al., "PREGNANCY OUTCOME AFTER TRANSCERVICAL CVS WITH A FLEXIBLE BIOPSY FORCEPS - EVALUATION OF RISK-FACTORS", Prenatal diagnosis, 15(9), 1995, pp. 809-816
28. SIJMONS RH; SIKKEMARADDATZ B; KLOOSTERMAN MD; BRIET JW; DEJONG B; LESCHOT NJ
    46,XY,DUP(10Q) IN DIRECT CVS PREPARATION AND MOSAIC 48,XXXY,DUP(10Q) IN CVS LONG-TERM CULTURE AND FETAL TISSUE
    Prenatal diagnosis
    
    R.H. Sijmons et al., "46,XY,DUP(10Q) IN DIRECT CVS PREPARATION AND MOSAIC 48,XXXY,DUP(10Q) IN CVS LONG-TERM CULTURE AND FETAL TISSUE", Prenatal diagnosis, 15(3), 1995, pp. 285-290
29. HANSSON K; SCHURINGBLOM GH; LESCHOT NJ
    THE PRESERVING OF CHORIONIC VILLI BEFORE ESTABLISHING LONG-TERM CELL-CULTURES FOR CYTOGENETIC ANALYSIS
    Prenatal diagnosis
    
    K. Hansson et al., "THE PRESERVING OF CHORIONIC VILLI BEFORE ESTABLISHING LONG-TERM CELL-CULTURES FOR CYTOGENETIC ANALYSIS", Prenatal diagnosis, 15(11), 1995, pp. 1067-1069
30. LESCHOT NJ; DEGROOT CJ
    OORTHUYS,HANNA,W.E.,MD (1943-1992) - IN-MEMORIAM
    American journal of medical genetics
    
    N.J. Leschot e C.J. Degroot, "OORTHUYS,HANNA,W.E.,MD (1943-1992) - IN-MEMORIAM", American journal of medical genetics, 57(4), 1995, pp. 525-526
31. AALFS CM; HOOVERS JMN; NIESTEOTTER MA; MANNENS HMAM; HENNEKAM RCM; LESCHOT NJ
    FURTHER DELINEATION OF THE PARTIAL PROXIMAL TRISOMY 10Q SYNDROME
    Journal of Medical Genetics
    
    C.M. Aalfs et al., "FURTHER DELINEATION OF THE PARTIAL PROXIMAL TRISOMY 10Q SYNDROME", Journal of Medical Genetics, 32(12), 1995, pp. 968-971
32. DELOZIERBLANCHET CD; FRANCIPANE L; MORRIS MA; HOOVERS JMN; LESCHOT NJ; COX JN
    TRISOMY-3 MOSAICISM ON CVS - CASE-REPORT WITH LITERATURE-REVIEW AND PROPOSITIONS FOR INVESTIGATION AND COUNSELING
    Clinical genetics
    
    C.D. Delozierblanchet et al., "TRISOMY-3 MOSAICISM ON CVS - CASE-REPORT WITH LITERATURE-REVIEW AND PROPOSITIONS FOR INVESTIGATION AND COUNSELING", Clinical genetics, 48(6), 1995, pp. 308-312
33. SCHURINGBLOM GH; KEIJZER M; JAKOBS ME; VANDENBRANDE DM; VISSER HM; WIEGANT J; HOOVERS JMN; LESCHOT NJ
    MOLECULAR CYTOGENETIC ANALYSIS OF TERM PLACENTAE SUSPECTED OF MOSAICISM USING FLUORESCENCE IN-SITU HYBRIDIZATION
    Prenatal diagnosis
    
    G.H. Schuringblom et al., "MOLECULAR CYTOGENETIC ANALYSIS OF TERM PLACENTAE SUSPECTED OF MOSAICISM USING FLUORESCENCE IN-SITU HYBRIDIZATION", Prenatal diagnosis, 13(8), 1993, pp. 671-679