-
1
-
-
0017692771
-
Frequency of chromosomal abnormalities in miscarriages and perinatal deaths
-
E.D. Alberman M.R. Creasy Frequency of chromosomal abnormalities in miscarriages and perinatal deaths J. Med. Genet. 14 1977 313-315
-
(1977)
J. Med. Genet.
, vol.14
, pp. 313-315
-
-
Alberman, E.D.1
Creasy, M.R.2
-
2
-
-
0035985727
-
Presumptive monosomy 21 with neuronal migration disorder re-diagnosed as de novo unbalanced translocation t(18p;21q) by fluorescence in situ hybridization
-
M. Alkan G.P. Ramelli H. Hirsiger I. Kese L. Remonda E.M. Bühler H. Moser Presumptive monosomy 21 with neuronal migration disorder re-diagnosed as de novo unbalanced translocation t(18p;21q) by fluorescence in situ hybridization Genet. Counsel. 13 2002 151-156
-
(2002)
Genet. Counsel.
, vol.13
, pp. 151-156
-
-
Alkan, M.1
Ramelli, G.P.2
Hirsiger, H.3
Kese, I.4
Remonda, L.5
Bühler, E.M.6
Moser, H.7
-
3
-
-
0033851760
-
Morphology and DNA content analysis in the evaluation of first trimester placentas for partial hydatiform mole (PHM)
-
S.H. Chew E.J. Perlman R. Williams R.J. Kurman B.M. Ronnett Morphology and DNA content analysis in the evaluation of first trimester placentas for partial hydatiform mole (PHM) Hum. Pathol. 31 8 2000 914-924
-
(2000)
Hum. Pathol.
, vol.31
, Issue.8
, pp. 914-924
-
-
Chew, S.H.1
Perlman, E.J.2
Williams, R.3
Kurman, R.J.4
Ronnett, B.M.5
-
4
-
-
0024370092
-
Immunohistochemical assessment of estrogen and progesterone receptors in stored imprints and cryostat sections of breast carcinomas
-
C.M. DeRosa L. Ozzello D.V. Habif J.G. Konrath G.L. Greene Immunohistochemical assessment of estrogen and progesterone receptors in stored imprints and cryostat sections of breast carcinomas Ann. Surg. 210 1989 224-228
-
(1989)
Ann. Surg.
, vol.210
, pp. 224-228
-
-
DeRosa, C.M.1
Ozzello, L.2
Habif, D.V.3
Konrath, J.G.4
Greene, G.L.5
-
5
-
-
0035878547
-
Chromosomal gains and losses are uncommon in hairy cell leukemia; a study based on comparative genomic hybridization and interphase fluorescence in situ hybridization
-
J. Dierlamm M. Stefanova I. Wlodarska L. Michaux K. Hinz E.M. Penas B. Maes A. Hagemeijer C. De Wolf-Peeters D.K. Hossfeld Chromosomal gains and losses are uncommon in hairy cell leukemia; a study based on comparative genomic hybridization and interphase fluorescence in situ hybridization Cancer Genet. Cytogenet. 128 2 2001 164-167
-
(2001)
Cancer Genet. Cytogenet.
, vol.128
, Issue.2
, pp. 164-167
-
-
Dierlamm, J.1
Stefanova, M.2
Wlodarska, I.3
Michaux, L.4
Hinz, K.5
Penas, E.M.6
Maes, B.7
Hagemeijer, A.8
De Wolf-Peeters, C.9
Hossfeld, D.K.10
-
6
-
-
0035935629
-
FISH characterization of a supernumerary r(1)(::cen->q22::q22->sq21::) chromosome associated with multiple anomalies and bilateral cataracts
-
P. Finelli P. Cavalli D. Giardino G. Gottardi F. Natacci S. Savasta L. Larissa FISH characterization of a supernumerary r(1)(:QCen->q22::q22->sq21::) chromosome associated with multiple anomalies and bilateral cataracts Am. J. Med. Genet. 104 2 2001 157-164
-
(2001)
Am. J. Med. Genet.
, vol.104
, Issue.2
, pp. 157-164
-
-
Finelli, P.1
Cavalli, P.2
Giardino, D.3
Gottardi, G.4
Natacci, F.5
Savasta, S.6
Larissa, L.7
-
7
-
-
0036468296
-
Occurrence of chromosome 9 and p53 alterations in multifocal dysplasia and carcionoma in situ of human urinary bladder
-
A. Hartmann G. Schlake D. Zaak E. Hungerhuber A. Hofstetter F. Hofstaedter R. Knuechel Occurrence of chromosome 9 and p53 alterations in multifocal dysplasia and carcionoma in situ of human urinary bladder Cancer Res. 62 3 2002 809-818
-
(2002)
Cancer Res.
, vol.62
, Issue.3
, pp. 809-818
-
-
Hartmann, A.1
Schlake, G.2
Zaak, D.3
Hungerhuber, E.4
Hofstetter, A.5
Hofstaedter, F.6
Knuechel, R.7
-
8
-
-
0024710120
-
Holoprosencephaly, polydactyly and normal chromosomes: Pseudo-trisomy 13?
-
B.G. Hewitt M.J. Seller C.P. Bennett D.M. Maxwell Holoprosencephaly, polydactyly and normal chromosomes: Pseudo-trisomy 13? Clin. Genet. 36 1989 141-143
-
(1989)
Clin. Genet.
, vol.36
, pp. 141-143
-
-
Hewitt, B.G.1
Seller, M.J.2
Bennett, C.P.3
Maxwell, D.M.4
-
9
-
-
0032946214
-
Investigation of chromosomal aberrations in hepatocellular carcinoma by fluorescence in situ hybridization
-
S.F. Huang H.C. Hsu J.A. Fletcher Investigation of chromosomal aberrations in hepatocellular carcinoma by fluorescence in situ hybridization Cancer Genet. Cytogenet. 111 1999 21-27
-
(1999)
Cancer Genet. Cytogenet.
, vol.111
, pp. 21-27
-
-
Huang, S.F.1
Hsu, H.C.2
Fletcher, J.A.3
-
10
-
-
0030965056
-
Effect of fixation on interphase cytogenetic analysis by direct fluorescence in situ hybridization on cell imprints
-
N. Kapranos G. Kontogeorgos K. Frangia E. Kokka Effect of fixation on interphase cytogenetic analysis by direct fluorescence in situ hybridization on cell imprints Biotech. Histochem. 72 1997 148-151
-
(1997)
Biotech. Histochem.
, vol.72
, pp. 148-151
-
-
Kapranos, N.1
Kontogeorgos, G.2
Frangia, K.3
Kokka, E.4
-
11
-
-
0001259866
-
The perinatal autopsy
-
J.W. Keeling (Ed.). first ed Springer London
-
J.W. Keeling The perinatal autopsy, in: J.W. Keeling (Ed.). Fetal and Neonatal Pathology first ed 1987 Springer London 1-43
-
(1987)
Fetal and Neonatal Pathology
, pp. 1-43
-
-
Keeling, J.W.1
-
13
-
-
0036381652
-
Atypical lipomatous tumor in 14-year-old patient: Distinction from lipoblastoma using FISH analysis
-
C. Kuhnen T. Mentzel A. Fisseler-Eckhoff M. Debiec-Rychter R. Sciot Atypical lipomatous tumor in 14-year-old patient: Distinction from lipoblastoma using FISH analysis Virchows Arch. 441 3 2002 299-302
-
(2002)
Virchows Arch.
, vol.441
, Issue.3
, pp. 299-302
-
-
Kuhnen, C.1
Mentzel, T.2
Fisseler-Eckhoff, A.3
Debiec-Rychter, M.4
Sciot, R.5
-
14
-
-
0017231757
-
Chromosome anomalies of infants dying during the perinatal period and premature newborn
-
N.P. Kuleshov Chromosome anomalies of infants dying during the perinatal period and premature newborn Hum. Genet. 31 1976 151-160
-
(1976)
Hum. Genet.
, vol.31
, pp. 151-160
-
-
Kuleshov, N.P.1
-
15
-
-
0036366826
-
Detection of c-erB-2 (HER-2/neu) amplification in breast carcionoma by fluorescence in situ hybridization on tissue sections and imprinted cells
-
K. Kunitomo T. Takehana S. Inoue H. Fujii S. Suzuki Y. Matsumoto A. Ooi Detection of c-erB-2 (HER-2/neu) amplification in breast carcionoma by fluorescence in situ hybridization on tissue sections and imprinted cells Pathol. Int. 52 7 2002 451-457
-
(2002)
Pathol. Int.
, vol.52
, Issue.7
, pp. 451-457
-
-
Kunitomo, K.1
Takehana, T.2
Inoue, S.3
Fujii, H.4
Suzuki, S.5
Matsumoto, Y.6
Ooi, A.7
-
16
-
-
0028849455
-
Use of fluorescence in situ hybridization (FISH) in the diagnosis of DiGeorge sequence and related diseases
-
R.S. Larson M.G. Butler Use of fluorescence in situ hybridization (FISH) in the diagnosis of DiGeorge sequence and related diseases Diagn. Mol. Pathol. 4 1995 274-278
-
(1995)
Diagn. Mol. Pathol.
, vol.4
, pp. 274-278
-
-
Larson, R.S.1
Butler, M.G.2
-
17
-
-
0027211943
-
Use of fluorescence in situ hybridization for retrospective detection of aneuploidy in multiple myeloma
-
W. Lee K. Han R.M. Drut C. Harris L. Meisner Use of fluorescence in situ hybridization for retrospective detection of aneuploidy in multiple myeloma Genes Chromosomes Cancer 7 3 1993 137-143
-
(1993)
Genes Chromosomes Cancer
, vol.7
, Issue.3
, pp. 137-143
-
-
Lee, W.1
Han, K.2
Drut, R.M.3
Harris, C.4
Meisner, L.5
-
19
-
-
0020071675
-
The immunoperoxidase method for rapid diagnosis of Herpes simplex encephalitis (HSE) using touch preparations
-
K.H. Merkel M. Zimmer The immunoperoxidase method for rapid diagnosis of Herpes simplex encephalitis (HSE) using touch preparations Am. J. Clin. Pathol. 77 1982 605-607
-
(1982)
Am. J. Clin. Pathol.
, vol.77
, pp. 605-607
-
-
Merkel, K.H.1
Zimmer, M.2
-
20
-
-
0037308632
-
Fluorescence in situ hybridizations for detecting TP16 MTS1/CDK 41 gene deletions in squamous cell carcinoma of the head and neck
-
A. Namazie S. Alavi N. Aghamohammadi M. Aghamohammadi T.C. Calcaterra M.B. Wang E.S. Srivatson Fluorescence in situ hybridizations for detecting TP16 MTS1/CDK 41 gene deletions in squamous cell carcinoma of the head and neck Cancer Genet. Cytogenet. 141 1 2003 49-55
-
(2003)
Cancer Genet. Cytogenet.
, vol.141
, Issue.1
, pp. 49-55
-
-
Namazie, A.1
Alavi, S.2
Aghamohammadi, N.3
Aghamohammadi, M.4
Calcaterra, T.C.5
Wang, M.B.6
Srivatson, E.S.7
-
21
-
-
0029597872
-
Trisomy 1 and 8 occur frequently in hepatocellular carcinoma but not in liver cell adenoma and focal nodular hyperplasia. A fluorescence in situ hybridization study
-
A. Nasarek M. Werner M. Nolte J. Klempnauer A. Georgii Trisomy 1 and 8 occur frequently in hepatocellular carcinoma but not in liver cell adenoma and focal nodular hyperplasia. A fluorescence in situ hybridization study Virchows Arch. 427 1995 373-378
-
(1995)
Virchows Arch.
, vol.427
, pp. 373-378
-
-
Nasarek, A.1
Werner, M.2
Nolte, M.3
Klempnauer, J.4
Georgii, A.5
-
22
-
-
0036480714
-
Prenatal diagnosis of tetralogy of Fallot associated with chromosome 22q11 deletion
-
D.C. Oh J.Y. Min M.H. Lee Y.M. Kim S.Y. Park H.S. Won I.K. Kim Y.H. Lee S.J. Yoo H.M. Ryu Prenatal diagnosis of tetralogy of Fallot associated with chromosome 22q11 deletion J. Korean Med. Sci. 17 1 2002 125-128
-
(2002)
J. Korean Med. Sci.
, vol.17
, Issue.1
, pp. 125-128
-
-
Oh, D.C.1
Min, J.Y.2
Lee, M.H.3
Kim, Y.M.4
Park, S.Y.5
Won, H.S.6
Kim, I.K.7
Lee, Y.H.8
Yoo, S.J.9
Ryu, H.M.10
-
23
-
-
0034755952
-
Differentiation of Candida albicans and Candida dubliniensis by fluorescent in situ hybridization with peptide nucleic acid probes
-
K. Oliveira G. Haase C. Kurtzman J.J. Hyldig-Nielsen H. Stender Differentiation of Candida albicans and Candida dubliniensis by fluorescent in situ hybridization with peptide nucleic acid probes J. Clin. Microbiol. 39 2001 4138-4141
-
(2001)
J. Clin. Microbiol.
, vol.39
, pp. 4138-4141
-
-
Oliveira, K.1
Haase, G.2
Kurtzman, C.3
Hyldig-Nielsen, J.J.4
Stender, H.5
-
24
-
-
0036080936
-
A new method to extract nuclei from paraffin-embedded tissue to study lymphomas using interphase fluorescence in situ hybridization
-
S.F. Paternoster S.R. Brockman R.F. McClure E.D. Remstein P.J. Kurtin G.W. Dewald A new method to extract nuclei from paraffin-embedded tissue to study lymphomas using interphase fluorescence in situ hybridization Am. J. Pathol. 160 6 2002 1967-1972
-
(2002)
Am. J. Pathol.
, vol.160
, Issue.6
, pp. 1967-1972
-
-
Paternoster, S.F.1
Brockman, S.R.2
McClure, R.F.3
Remstein, E.D.4
Kurtin, P.J.5
Dewald, G.W.6
-
25
-
-
0343319476
-
Fluorescence in situ hybridization with human chromosome-specific libraries: Detection of trisomy of 21 and translocations of chromosome 4
-
D. Pinkel J. Landegent C. Collins J. Fuscoe R. Segraves J. Lucas J. Gray Fluorescence in situ hybridization with human chromosome-specific libraries: Detection of trisomy of 21 and translocations of chromosome 4 Proc. Natl. Acad. Sci. USA 85 1988 9138-9142
-
(1988)
Proc. Natl. Acad. Sci. USA
, vol.85
, pp. 9138-9142
-
-
Pinkel, D.1
Landegent, J.2
Collins, C.3
Fuscoe, J.4
Segraves, R.5
Lucas, J.6
Gray, J.7
-
26
-
-
0036120928
-
Interphase luorescence in situ hybridization and DNA flow cytometry analysis of medulloblastomas with a normal karyotype
-
E. Rajcan-Separovic G. Hendson S. Tang E. Seto T. Thomson D. Phillips D. Kalousek Interphase luorescence in situ hybridization and DNA flow cytometry analysis of medulloblastomas with a normal karyotype Cancer Genet. Cytogenet. 133 1 2002 94-97
-
(2002)
Cancer Genet. Cytogenet.
, vol.133
, Issue.1
, pp. 94-97
-
-
Rajcan-Separovic, E.1
Hendson, G.2
Tang, S.3
Seto, E.4
Thomson, T.5
Phillips, D.6
Kalousek, D.7
-
27
-
-
14644403323
-
DNA extraction and quantification from touch and scrape preparations obtained from autopsy liver cells
-
in press
-
C.N.M. Ribeiro, L.C. Peres, J.M. Pina-Neto, DNA extraction and quantification from touch and scrape preparations obtained from autopsy liver cells, Braz. J. Med. Biol. Res. (2002), in press
-
(2002)
Braz. J. Med. Biol. Res.
-
-
Ribeiro, C.N.M.1
Peres, L.C.2
Pina-Neto, J.M.3
-
28
-
-
0035079006
-
De novo unbalanced t(11q;21q) leading to a partial monosomy 21pter-q22.2 and 11q24-qter in a patient initially diagnosed as monosomy 21
-
M. Riegel A. Baumer A. Piram D. Ortolan L.C. Peres J.M. Pina-Neto De novo unbalanced t(11q;21q) leading to a partial monosomy 21pter-q22.2 and 11q24-qter in a patient initially diagnosed as monosomy 21, Genet. Counsel. 12 2001 69-75
-
(2001)
Genet. Counsel.
, vol.12
, pp. 69-75
-
-
Riegel, M.1
Baumer, A.2
Piram, A.3
Ortolan, D.4
Peres, L.C.5
Pina-Neto, J.M.6
-
30
-
-
0022989733
-
Human teratoagenicity
-
T.H. Shepard Human teratoagenicity Adv. Pediatr. 33 1986 225-268
-
(1986)
Adv. Pediatr.
, vol.33
, pp. 225-268
-
-
Shepard, T.H.1
-
31
-
-
0035693147
-
A light and electron microscopic histopathological study of human bladder mucosa after intravesical resinferatoxin application
-
C. Silva A. Avelino C. Souto-Moura F. Cruz A light and electron microscopic histopathological study of human bladder mucosa after intravesical resinferatoxin application BJU Int. 88 2001 355-360
-
(2001)
BJU Int.
, vol.88
, pp. 355-360
-
-
Silva, C.1
Avelino, A.2
Souto-Moura, C.3
Cruz, F.4
-
32
-
-
0028267297
-
Rapid detection of prognostic genetic factors in neuroblastoma using fluorescence in situ hybridization on tumour imprints and bone marrow smears
-
C.P.F. Taylor A.G. McGuckin N.P. Bown M.M. Reid A.J. Malcolm A.D.J. Pearson D. Sheer Rapid detection of prognostic genetic factors in neuroblastoma using fluorescence in situ hybridization on tumour imprints and bone marrow smears Br. J. Cancer 69 1994 445-451
-
(1994)
Br. J. Cancer
, vol.69
, pp. 445-451
-
-
Taylor, C.P.F.1
McGuckin, A.G.2
Bown, N.P.3
Reid, M.M.4
Malcolm, A.J.5
Pearson, A.D.J.6
Sheer, D.7
-
33
-
-
0036841057
-
Genomic gain of PIK3CA and increased expression of p110 alpha are associated with progression of dysplasia into invasive squamous cell carcinoma
-
J. Woenckhaus K. Steger E. Werner I. Fenic U. Gamaerdinger T. Dreyer U. Stahl Genomic gain of PIK3CA and increased expression of p110 alpha are associated with progression of dysplasia into invasive squamous cell carcinoma J. Pathol. 198 3 2002 335-342
-
(2002)
J. Pathol.
, vol.198
, Issue.3
, pp. 335-342
-
-
Woenckhaus, J.1
Steger, K.2
Werner, E.3
Fenic, I.4
Gamaerdinger, U.5
Dreyer, T.6
Stahl, U.7
-
34
-
-
0035882367
-
Deletions at chromosome regions 7q11.23 and 7q36 in a patient with Williams syndrome
-
C.H. Wouters H.J. Meijers-Heijboer B.J. Eussen A.A. van der Heide R.B. van Luijk E. van Drunen B.B. Beverloo F. Visscher J.O. Van Hemel Deletions at chromosome regions 7q11.23 and 7q36 in a patient with Williams syndrome Am. J. Med. Genet. 102 3 2001 261-265
-
(2001)
Am. J. Med. Genet.
, vol.102
, Issue.3
, pp. 261-265
-
-
Wouters, C.H.1
Meijers-Heijboer, H.J.2
Eussen, B.J.3
van der Heide, A.A.4
van Luijk, R.B.5
van Drunen, E.6
Beverloo, B.B.7
Visscher, F.8
Van Hemel, J.O.9
-
35
-
-
0028799264
-
Novel fluorescence in situ hybridization approaches in solid tumors. Characterization of frozen specimens, touch preparations, and cytological preparations
-
S. Xiao A. Renshaw E.S. Cibas T.J. Hudson J.A. Fletcher Novel fluorescence in situ hybridization approaches in solid tumors. Characterization of frozen specimens, touch preparations, and cytological preparations Am. J. Pathol. 147 1995 896-904
-
(1995)
Am. J. Pathol.
, vol.147
, pp. 896-904
-
-
Xiao, S.1
Renshaw, A.2
Cibas, E.S.3
Hudson, T.J.4
Fletcher, J.A.5
-
36
-
-
0027492416
-
Liver-derived fetal hematopoietic stem cells selectively and preferentially home to the fetal bone marrow
-
E.D. Zanjani J.L. Ascensao M. Tavassoli Liver-derived fetal hematopoietic stem cells selectively and preferentially home to the fetal bone marrow Blood 81 1993 399-404
-
(1993)
Blood
, vol.81
, pp. 399-404
-
-
Zanjani, E.D.1
Ascensao, J.L.2
Tavassoli, M.3
|