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Results of search for 'au:"Stumm, M"', page 1 of 3
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Authors
Albig, M
Allhoff, E P
Antoccia, A
Becker, R
Chrzanowska, K H
Chudoba, I
Entezami, M
Gatti, R A
Jakubiczka, S
Krebs, P
Liehr, T
Müsebeck, J
Reis, A
Sperling, K
Stumm, M
Tönnies, H
Volleth, M
Wegner, R D
Wieacker, P
Wieacker, P F
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Adolescent
Adult
Animals
Ataxia Telangiectasia
Child
Child, Preschool
Chromosome Aberrations
Chromosome Banding
Chromosome Breakage
Chromosome Mapping
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Humans
In Situ Hybridization, Fluorescence
Karyotyping
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Your search returned 58 results.
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1.
[Portal hypertension and angiogenesis].
[electronic resource]
by
Stumm, M
Sieber, C
Producer:
20000420
In:
Schweizerische medizinische Wochenschrift
vol. 130
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2.
[Prenatal diagnostics: current medical aspects].
[electronic resource]
by
Stumm, M
Entezami, M
Producer:
20150406
In:
Bundesgesundheitsblatt, Gesundheitsforschung, Gesundheitsschutz
vol. 56
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3.
Noncomplementation of radiation-induced chromosome aberrations in ataxia-telangiectasia/ataxia-telangiectasia-variant heterodikaryons.
[electronic resource]
by
Stumm, M
Sperling, K
Wegner, R D
Producer:
19970603
In:
American journal of human genetics
vol. 60
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4.
Molecular cytogenetic techniques for the diagnosis of chromosomal abnormalities in childhood disease.
[electronic resource]
by
Stumm, M
Tönnies, H
Wieacker, P F
Producer:
19990824
In:
European journal of pediatrics
vol. 158
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5.
Multi-locus (ML)-FISH is a reliable tool for nondisjunction studies in human oocytes.
[electronic resource]
by
Eckel, H
Kleinstein, J
Wieacker, P
Stumm, M
Producer:
20040528
In:
Cytogenetic and genome research
vol. 103
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6.
Interphase M-FISH applications using commercial probes in prenatal and PGD diagnostics.
[electronic resource]
by
Stumm, M
Wegner, R-D
Bloechle, M
Eckel, H
Producer:
20060918
In:
Cytogenetic and genome research
vol. 114
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7.
Genotype/phenotype correlation in a patient with partial monosomy 15 and partial trisomy 14.
[electronic resource]
by
Volleth, M
Stumm, M
Bürger, J
Muschke, P
Wieacker, P
Producer:
20050621
In:
Cytogenetic and genome research
vol. 108
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8.
Two Decades of Endovascular Repair of Popliteal Artery Aneurysm--A Meta-analysis.
[electronic resource]
by
von Stumm, M
Teufelsbauer, H
Reichenspurner, H
Debus, E S
Producer:
20151116
In:
European journal of vascular and endovascular surgery : the official journal of the European Society for Vascular Surgery
vol. 50
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9.
Suspicious Prenasal Skin Thickness-to-Nasal Bone Length Ratio: Prevalence and Correlation with Other Markers in Second and Third Trimester Fetuses with Down Syndrome.
[electronic resource]
by
Hagen, A
Albig, M
Keller, T
Stumm, M
Entezami, M
Producer:
20160901
In:
Ultraschall in der Medizin (Stuttgart, Germany : 1980)
vol. 36
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10.
[Trisomy 4p as result of a maternal translocation t(4;8)(q11;p23)].
[electronic resource]
by
Stumm, M
Reuter, M
Mandon, U
Brückner, R
Wieacker, P
Producer:
19990407
In:
Klinische Padiatrie
vol. 211
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11.
High reliability and sensitivity of the BCR/ABL1 D-FISH test for the detection of BCR/ABL rearrangements.
[electronic resource]
by
Pelz, A F
Kröning, H
Franke, A
Wieacker, P
Stumm, M
Producer:
20020606
In:
Annals of hematology
vol. 81
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12.
Trisomy 8 mosaicism in a with patient tetraamelia.
[electronic resource]
by
Götze, A
Krebs, P
Stumm, M
Wieacker, P
Allhoff, E P
Producer:
19991105
In:
American journal of medical genetics
vol. 86
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13.
A novel translocation (17;19)(p13;p13) in a patient with acute myelomonocytic leukemia.
[electronic resource]
by
Brückner, R
Jentsch-Ullrich, K
Franke, A
Wieacker, P
Stumm, M
Producer:
20000608
In:
Cancer genetics and cytogenetics
vol. 119
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14.
Impaired p53-mediated DNA damage response, cell-cycle disturbance and chromosome aberrations in Nijmegen breakage syndrome lymphoblastoid cell lines.
[electronic resource]
by
Antoccia, A
Stumm, M
Saar, K
Ricordy, R
Maraschio, P
Tanzarella, C
Producer:
19990629
In:
International journal of radiation biology
vol. 75
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15.
Comparative genomic hybridization based strategy for the analysis of different chromosome imbalances detected in conventional cytogenetic diagnostics.
[electronic resource]
by
Tönnies, H
Stumm, M
Wegner, R D
Chudoba, I
Kalscheuer, V
Neitzel, H
Producer:
20011004
In:
Cytogenetics and cell genetics
vol. 93
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16.
Preferential inactivation of a dupX(q23 --> q27-28) chromosome in a girl with mental retardation and dysmorphy.
[electronic resource]
by
Volleth, M
Stumm, M
Mohnike, K
Kalscheuer, V M
Jakubiczka, S
Wieacker, P
Producer:
20011207
In:
Human heredity
vol. 52
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17.
G2-phase radiation response in lymphoblastoid cell lines from Nijmegen breakage syndrome.
[electronic resource]
by
Antoccia, A
di Masi, A
Maraschio, P
Stumm, M
Ricordy, R
Tanzarella, C
Producer:
20020502
In:
Cell proliferation
vol. 35
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18.
High frequency of spontaneous translocations revealed by FISH in cells from patients with the cancer-prone syndromes ataxia telangiectasia and Nijmegen breakage syndrome.
[electronic resource]
by
Stumm, M
Neubauer, S
Keindorff, S
Wegner, R D
Wieacker, P
Sauer, R
Producer:
20010802
In:
Cytogenetics and cell genetics
vol. 92
Online resources:
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19.
Mosaic tetrasomy 9p in a girl with multiple congenital anomalies: cytogenetic and molecular-cytogenetic studies.
[electronic resource]
by
Stumm, M
Tönnies, H
Mandon, U
Götze, A
Krebs, P
Wieacker, P F
Producer:
19990824
In:
European journal of pediatrics
vol. 158
Online resources:
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20.
Partial trisomy/monosomy 6q in fetal cells and CVS long-term culture not present in CVS short-term culture.
[electronic resource]
by
Wegner, R D
Schröck, E
Obladen, M
Becker, R
Stumm, M
Sperling, K
Producer:
19970117
In:
Prenatal diagnosis
vol. 16
Online resources:
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