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1. The worth of a child
by Murray, Thomas H., 1946
1996, ISBN 0520088360, xiv, 207
Ethics | Parent and child | Moral and ethical aspects | Parenthood | Childbirth | Children and adults | Eltern | Kind
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2. Image analysis system and its use in cytogenetic analysis
by Ahmad, Equebal and Kucheria, Kiran
Image analysis system and its use in cytogenetic analysis, 12/2002
Cytogenetic analysis is an important tool in the diagnosis of genetic disorders. It involves cell culture, metaphase arrest, hypotonic treatment, cell... 
Image analysis system, cytogenetics, karyotyping
Journal
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3. Chromosome analysis protocols
by Gosden, John R and SpringerLink (Online service)
1994, Methods in molecular biology, ISBN 0896032892, Volume 29., xi, 508
Chromosomes, as the genetic vehicles, provide the basic material for a large proportion of genetic investigations, from the construction of gene maps and... 
Human cytogenetics | Cytogenetics | Research | Technique | Methodology | Chromosomes | Human genetics | Human Genetics | Biomedicine
Book
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4. Full Text Nonmammalian genomic analysis
: a practical guide
by Birren, Bruce W and Lai, Eric Hon Cheong, 1957
1996, ISBN 0121012859, 369
Offering detailed protocols for those needing to construct a variety of maps and isolate genes, this unique book is intended to popularize the new techniques... 
Microbial genetics | Gene mapping | Laboratory manuals | Plant genetics | Biology, life sciences
eBook
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5. Full Text Additional information from chromosomal microarray analysis (CMA) over conventional karyotyping when diagnosing chromosomal abnormalities in miscarriage: a systematic review and meta‐analysis
by Dhillon, RK and Hillman, SC and Morris, RK and McMullan, D and Williams, D and Coomarasamy, A and Kilby, MD
BJOG: An International Journal of Obstetrics & Gynaecology, ISSN 1470-0328, 01/2014, Volume 121, Issue 1, pp. 11 - 21
BackgroundApproximately 50% of spontaneous miscarriages are associated with chromosome abnormalities. Identification of these karyotypic abnormalities helps to... 
microarray | karyotyping | array | CGH | miscarriage | CMA | arrayCGH | GENETIC-ANALYSIS | ARRAY-CGH | SPONTANEOUS-ABORTIONS | COMPARATIVE GENOMIC HYBRIDIZATION | OBSTETRICS & GYNECOLOGY | Karyotyping - methods | Microarray Analysis - methods | Pregnancy | Abortion, Spontaneous - genetics | Humans | Chromosome Aberrations | Chromosome Disorders - diagnosis | Female | Comparative Genomic Hybridization - methods | DNA microarrays | Diagnosis | Miscarriage | Chromosomes | Analysis | Genomics | Cytogenetics | Systematic review | Medical diagnosis
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6. Full Text Statin therapy and plasma coenzyme Q10 concentrations—A systematic review and meta-analysis of placebo-controlled trials
by Banach, Maciej and Serban, Corina and Ursoniu, Sorin and Rysz, Jacek and Muntner, Paul and Toth, Peter P and Jones, Steven R and Rizzo, Manfredi and Glasser, Stephen P and Watts, Gerald F and Blumenthal, Roger S and Lip, Gregory Y.H and Mikhailidis, Dimitri P and Sahebkar, Amirhossein and Lipid & Blood Pressure and Lipid and Blood Pressure Meta-analysis Collaboration (LBPMC) Group
Pharmacological Research, ISSN 1043-6618, 09/2015, Volume 99, pp. 329 - 336
Statin therapy may lower plasma coenzyme Q10 (CoQ10) concentrations, but the evidence as to the significance of this effect is unclear. We assessed the impact... 
Mitochondrial dysfunction | Ubiquinone | Coenzyme Q10 | Statin therapy | Myopathy | COQ | ANTIOXIDANTS | INTOLERANCE | PEROXIDATION | DEFINITION. POSITION PAPER | SKELETAL-MUSCLE | PHARMACOLOGY & PHARMACY | COA-REDUCTASE INHIBITORS | SIMVASTATIN | Double-Blind Method | Placebo Effect | Humans | Middle Aged | Ubiquinone - analogs & derivatives | Male | Case-Control Studies | Randomized Controlled Trials as Topic | Ubiquinone - blood | Hydroxymethylglutaryl-CoA Reductase Inhibitors - therapeutic use | Adult | Female | Aged | Hypertension | Enzymes | Medical colleges | Drugstores | Family medicine | College teachers | Cardiovascular agents | Preventive health services | Prevention | Analysis | Pharmacy | Cytogenetics | Heart diseases | Medicine, Preventive | Statins
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7. Full Text Prognostic relevance of FLT3-TKD mutations in AML: The combination matters an analysis of 3082 patients
by Bacher, Ulrike and Haferlach, Claudia and Kern, Wolfgang and Haferlach, Torsten and Schnittger, Susanne
Blood, ISSN 0006-4971, 03/2008, Volume 111, Issue 5, pp. 2527 - 2537
We characterized the mutational status of the FLT3 tyrosine kinase domain (FLT3-TLD) in 3082 patients with newly diagnosed AML. FLT3-TKD mutations were... 
INTERNAL TANDEM DUPLICATION | STUDY-GROUP ULM | KINASE DOMAIN MUTATIONS | ACUTE MYELOGENOUS LEUKEMIA | ACTIVATING POINT MUTATIONS | NORMAL CYTOGENETICS | ACUTE MYELOID-LEUKEMIA | HEMATOLOGY | MINIMAL RESIDUAL DISEASE | RECEPTOR TYROSINE KINASE | ACUTE PROMYELOCYTIC LEUKEMIA | Protein Structure, Tertiary | Recurrence | Prognosis | Leukemia, Myeloid, Acute - pathology | Humans | Middle Aged | Survival Rate | Genetic Markers | Mutation - genetics | fms-Like Tyrosine Kinase 3 - chemistry | Leukemia, Myeloid, Acute - mortality | fms-Like Tyrosine Kinase 3 - genetics | Thermodynamics | Leukemia, Myeloid, Acute - diagnosis | DNA Mutational Analysis | Karyotyping | Adolescent | Aged, 80 and over | Adult | Aged | Neoplasm Proteins - genetics | Leukemia, Myeloid, Acute - genetics
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8. Full Text Added value of chromosomal microarray analysis over conventional karyotyping in stillbirth work‐up: systematic review and meta‐analysis
by Martinez‐Portilla, R. J and Pauta, M and Hawkins‐Villarreal, A and Rial‐Crestelo, M and Paz y Miño, F and Madrigal, I and Figueras, F and Borrell, A
Ultrasound in Obstetrics & Gynecology, ISSN 0960-7692, 05/2019, Volume 53, Issue 5, pp. 590 - 597
This article's abstract has been translated into Spanish and Chinese. Follow the links from the abstract to view the translations. 
stillbirth | microarray | single‐proportion meta‐analysis | qfPCR | CMA | G‐banding karyotype | single-proportion meta-analysis | G-banding karyotype | GENETIC EVALUATION | ARRAY | ABNORMALITIES | DEATH | CYTOGENETIC ANALYSIS | OBSTETRICS & GYNECOLOGY | ACOUSTICS | PRODUCTS | FETUSES | COMPARATIVE GENOMIC HYBRIDIZATION | UTILITY | RADIOLOGY, NUCLEAR MEDICINE & MEDICAL IMAGING | PRENATAL-DIAGNOSIS | DNA microarrays | Still-birth | Chromosomes | Analysis | Sensitivity analysis | Identification methods | Fetuses | Stillbirth | Gestation | Subgroups | Genetic screening | Heterogeneity | Webs | Quality control | Diagnostic software | Diagnostic systems | Yield | Quality assessment | Added value | Anomalies
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9. Full Text Genomic analysis of the DNA replication timing program during mitotic S phase in maize (Zea mays) root tips
by Wear, Emily E and Song, Jawon and Zynda, Gregory J and LeBlanc, Chantal and Lee, Tae-Jin and Mickelson-Young, Leigh and Concia, Lorenzo and Mulvaney, Patrick and Szymanski, Eric S and Allen, George C and Martienssen, Robert A and Vaughn, Matthew W and Hanley-Bowdoin, Linda and Thompson, William F
Plant Cell, ISSN 1040-4651, 09/2017, Volume 29, Issue 9, pp. 2126 - 2149
All plants and animals must replicate their DNA, using a regulated process to ensure that their genomes are completely and accurately replicated. DNA... 
ARABIDOPSIS-THALIANA | SPATIOTEMPORAL ORGANIZATION | CHROMOSOMAL DOMAINS | BIOCHEMISTRY & MOLECULAR BIOLOGY | EMBRYONIC STEM | HUMAN TRANSCRIPTOME MAP | MAMMALIAN-CELLS | PLANT SCIENCES | CELL BIOLOGY | PLURIPOTENT STEM-CELLS | HIGHER-PLANT-CELLS | HISTONE H3 | GENE-EXPRESSION | Meristem - cytology | Zea mays - genetics | Genes, Plant | DNA Replication Timing - genetics | Genomics | Mitosis - genetics | S Phase - genetics | Zea mays - cytology | Meristem - genetics | Time Factors | Base Sequence | DNA Transposable Elements - genetics | Transcription, Genetic | Models, Genetic | Chromosomes, Plant - genetics | Tandem Repeat Sequences - genetics | DNA replication | Chromatin | DNA | Genetic research | Corn | Genomes | Genetic transcription | Plants | Chromosomes | Plant cytogenetics | Mitosis | Analysis | Physiological aspects | Genetic aspects | Yeast | Genomic analysis | Transcription | Nucleotide sequence | Knobs | Maize | Gene sequencing | DNA biosynthesis | Windows (intervals) | Heterochromatin | Replicating | S phase | Cell cycle | Replication | Deoxyribonucleic acid--DNA | Tips | Large-Scale Biology
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10. Full Text Genomic Imbalance in Products of Conception: Single-Nucleotide Polymorphism Chromosomal Microarray Analysis
by Levy, Brynn and Sigurjonsson, Styrmir and Pettersen, Barbara and Maisenbacher, Melissa K and Hall, Megan P and Demko, Zachary and Lathi, Ruth B and Tao, Rosina and Aggarwal, Vimla and Rabinowitz, Matthew
Obstetrics & Gynecology, ISSN 0029-7844, 08/2014, Volume 124, Issue 2, PART 1, pp. 202 - 209
OBJECTIVE:To report the full cohort of identifiable anomalies, regardless of known clinical significance, in a large-scale cohort of postmiscarriage... 
1ST-TRIMESTER SPONTANEOUS-ABORTIONS | KARYOTYPES | DIAGNOSIS | MISCARRIAGES | DATABASE | VARIANTS | ABNORMALITIES | UNIPARENTAL DISOMY | HYBRIDIZATION | CYTOGENETIC ANALYSIS | OBSTETRICS & GYNECOLOGY | Abortion, Spontaneous - genetics | Oligonucleotide Array Sequence Analysis | Humans | Middle Aged | Uniparental Disomy | Aneuploidy | Genotyping Techniques | Pregnancy | Tetraploidy | Young Adult | Aborted Fetus | Adolescent | Chromosome Aberrations | Polymorphism, Single Nucleotide - genetics | Adult | Female | Triploidy
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11. Full Text Analysis for loss of heterozygosity on chromosome arm 13q by STR analysis or SNP sequencing can replace analysis of FLT3‐ITD to detect patients with prognostically adverse AML
by Schnittger, Susanne and Haferlach, Claudia and Kern, Wolfgang and Haferlach, Torsten
Genes, Chromosomes and Cancer, ISSN 1045-2257, 12/2014, Volume 53, Issue 12, pp. 1008 - 1017
We aimed at developing novel assays for Loss of Heterozygosity (LOH) detection on 13q as a substitute for FLT3 ‐ITD analysis to identify acute myeloid leukemia... 
INTERNAL TANDEM DUPLICATION | IMPACT | ONCOLOGY | LOAD | JUXTAMEMBRANE | SIZE | GENETICS & HEREDITY | ACUTE MYELOID-LEUKEMIA | MUTATIONS | INHIBITORS | SORAFENIB | CYTOGENETICS | Chromosomes, Human, Pair 13 - genetics | Prognosis | Leukemia, Myeloid, Acute - pathology | Humans | Middle Aged | Male | Loss of Heterozygosity | Sequence Analysis, DNA | Young Adult | fms-Like Tyrosine Kinase 3 - genetics | Leukemia, Myeloid, Acute - diagnosis | Adolescent | Aged, 80 and over | Adult | Female | Aged | Polymorphism, Single Nucleotide | Microsatellite Repeats | Cohort Studies | Genetic research | Analysis | Single nucleotide polymorphisms | Survival analysis | Medical research | Leukemia
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12. Full Text Outcome of older patients with acute myeloid leukemia: An Analysis of SEER Data over 3 Decades
by Thein, Mya S and Ershler, William B and Jemal, Ahmedin and Yates, Jerome W and Baer, Maria R
Cancer, ISSN 0008-543X, 08/2013, Volume 119, Issue 15, pp. 2720 - 2727
BACKGROUND Acute myeloid leukemia (AML) is the common form of acute leukemia in adults, accounting for over 80% of all acute leukemias in individuals aged >18... 
acute myeloid leukemia | age | Surveillance, Epidemiology and End Results data | survival | CYTOSINE-ARABINOSIDE | ACUTE MYELOCYTIC-LEUKEMIA | DAUNORUBICIN | CANCER | CYTOGENETICS | CHEMOTHERAPY TOXICITY | Epidemiology and End Results data | THERAPY | Surveillance | ONCOLOGY | GROUP-B | Leukemia, Myeloid, Acute - mortality | United States - epidemiology | SEER Program | Survival Rate - trends | Age Factors | Humans | Leukemia, Myeloid, Acute - drug therapy | Female | Male | Treatment Outcome | Aged | Incidence | Research | Epidemiology | Health aspects | Analysis | Survival after airplane accidents, shipwrecks, etc
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13. Full Text Full Karyotype Interphase Cell Analysis
by Baumgartner, Adi and Ferlatte Hartshorne, Christy and Polyzos, Aris A and Weier, Heinz-Ulrich G and Weier, Jingly Fung and O’Brien, Ben
Journal of Histochemistry & Cytochemistry, ISSN 0022-1554, 8/2018, Volume 66, Issue 8, pp. 595 - 606
Aneuploidy seems to play not only a decisive role in embryonal development but also in tumorigenesis where chromosomal and genomic instability reflect a... 
interphase nuclei | full karyotype analysis | chromosome enumeration | DNA probes | aneuploidy | FISH | spectral imaging | PREIMPLANTATION DIAGNOSIS | CHROMOSOMAL BREAKPOINTS | IN-SITU HYBRIDIZATION | HUMAN BLASTOCYSTS | CYTOGENETIC ANALYSIS | CELL BIOLOGY | HUMAN EMBRYOS | THYROID-CANCER | COMPARATIVE GENOMIC HYBRIDIZATION | Chromosomes, Artificial, Bacterial - genetics | Karyotyping - methods | Interphase | Single-Cell Analysis - methods | Humans | Plasmids - genetics | DNA Probes - genetics | Aneuploidy | Male | Image Processing, Computer-Assisted - methods | In Situ Hybridization, Fluorescence - methods | Karyotype
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14. Full Text Interphase fluorescent in situ hybridization deletion analysis of the 9p21 region and prognosis in childhood acute lymphoblastic leukaemia (ALL): results from a prospective analysis of 519 Nordic patients treated according to the NOPHO‐ALL 2000 protocol
by Kuchinskaya, Ekaterina and Heyman, Mats and Nordgren, Ann and Söderhäll, Stefan and Forestier, Erik and Wehner, Peder and Vettenranta, Kim and Jonsson, Olafur and Wesenberg, Finn and Sahlén, Sigrid and Nordenskjöld, Magnus and Blennow, Elisabeth and Medicinska fakulteten and Institutionen för klinisk vetenskap and Pediatrik and Umeå universitet
British Journal of Haematology, ISSN 0007-1048, 03/2011, Volume 152, Issue 5, pp. 615 - 622
Interphase fluorescent in situ hybridization (FISH) was applied on diagnostic BM smears from 519 children with acute lymphoblastic leukaemia (ALL) in order to... 
9p21 deletion | interphase fluorescent | hybridization | childhood acute lymphoblastic leukaemia | in situ | Childhood acute lymphoblastic leukaemia | Interphase fluorescent in situ hybridization | HOMOZYGOUS DELETION | P15(INK4B) DELETIONS | GENE REARRANGEMENTS | CDKN2A | interphase fluorescent in situ hybridization | INACTIVATION | RELAPSE | IMPACT | FREQUENT DELETION | MALIGNANCIES | COMPARATIVE GENOMIC HYBRIDIZATION | HEMATOLOGY | Chromosome Deletion | Precursor T-Cell Lymphoblastic Leukemia-Lymphoma - drug therapy | Prognosis | Prospective Studies | Humans | Child, Preschool | In Situ Hybridization, Fluorescence | Infant | Male | Treatment Outcome | Precursor B-Cell Lymphoblastic Leukemia-Lymphoma - genetics | Precursor Cell Lymphoblastic Leukemia-Lymphoma - genetics | Chromosomes, Human, Pair 9 - genetics | Precursor Cell Lymphoblastic Leukemia-Lymphoma - drug therapy | Precursor B-Cell Lymphoblastic Leukemia-Lymphoma - drug therapy | Antineoplastic Combined Chemotherapy Protocols - therapeutic use | Precursor T-Cell Lymphoblastic Leukemia-Lymphoma - genetics | Adolescent | Survival Analysis | Female | Child | Cytogenetics | Health aspects | Analysis | Pediatrics | Acute lymphatic leukemia | Lymphocytes B | Interphase | Fluorescence in situ hybridization | Oncology | Lymphocytes T | Children | Gene deletion | Age | childhood acute lymphoblastic leukaemia; 9p21 deletion; interphase fluorescent in situ hybridization
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