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Journal
Club List
The Journal Club order
form is now available on line to print from this web site.
READING LIST 21
- 1993
1. Cryptic Translocations and Telomeric Integrity.
2. Rapid Detection of Chromosome Aneuploid in Unculture Amniocytes
by using Fluorescence In Situ Hybridization (FISH).
3. A Prospective Cytogenetic Study of 36 Cases of Digeorge Syndrome.
READING LIST 22 - 1994
1. Uniparental Disomy for Chromosome 16 in Humans.
2. Flow Cytometric and Cytogenetic Analyses in Human Spontaneous
Abortions.
3. Constitutional 1p36 Deletion in a Child with Neuroblastoma.
READING LIST 23
- 1994
1. Characterization of Supernumerary Ringmarker Chromosome by
FISH.
2. A Rare Inherited Euchromatic Haleromorphism on Chromosome
One.
3. Attitudes of Women of Childbearing Age Towards Prenatal Diagnosis
in Southeastern France.
READING LIST 24
- 1994
1. Cytogenetic and Molecular Studies in the Prader-Willi and
Angelman Syndromes: An Overview.
2. Mosaic Isochromosome 8p.
3. Brief Clinical Report: Isochromosomes 18p in a Mother and
Her Child.
READING LIST 25
- 1995
1. An Extra Band Within the Human 9qh+ Region that Behaves Like
the Surrounding Constitutive Heterochromatin.
2. Diploid/Triploid Mosaicism: Further Delineation of the Phenotype.
3. Tetrasomy 12p (Pallister-Killian Syndrome): Ultrasound Indicators
and Confirmation by Interphase FISH.
READING LIST 26
- 1995
1. Satellited 4q Identified in Amniotic Fluid Cells
2. New Heritable Fragile Site with Spontaneous Expression at
1q41
3. Rapid Prenatal Diagnosis of 14 Cases of Triploidy Using FISH
with Multiple Probes
READING LIST 27 - 1995
1. Segregation of Frax E in a Large Family: Clinical, Psychometric,
Cytogenetic and Molecular Data
2. Karyotype Abnormalities in Fetuses Diagnosed as Abnormal on
Ultrasound Before 20 Weeks' Gestational Age
3. Mosaic Uniparental Disomy in Beckwith-Wiedemann Syndrome
READING LIST 28 - 1995
1. Prenatal Diagnosis of Trisomy 9. Six Cases and a Review of
the Literature
2. Sex Chromosome Loss and Aging: In Situ Hybridization Studies
on Human Interphase Nuclei
3. The Genetics of XX Gonadal Dysgenesis
READING LIST 29 - 1997
1. Meiotic Orgin of Trisomy in Confined Placental Mosaicism is
Correlated with Presence of Fetal Uniparental Disomy, High Levels
of Trisomy in Trophoblast, and Increased Risk of Fetal Intrauterine
Growth Restriction
2. Microdissection and DOP-PCR-based Reverse Chromosome Painting
as a Fast and Reliable Strategy in the Analysis of Various Structural
Chromosome Abnormalities.
3. Estimated Rates of and Indication for Postnatal Diagnosis
with Implications for Prenatal Counselling.
READING LIST 30
- 1999
1. Male Infertility and the Y Chromosome.
2. Gonadoblastoma, Testicular and Prostate Cancers, and the TSPY
Gene.
3. Genetics of Angelman Syndrome.
4. Noninvasive Test for Fragile X Syndrome, using hair root analysis.
READING LIST 31 2000
1. Parental origin and phenotype
of triploidy in spontaneous abortions: predominance of diandry
and association with the partial hydatidiform mole.
2. Jumping translocations in spontaneous abortions
3. Cytogenetics and mechanisms of spontaneous abortions: increased
apoptosis and decreased cell proliferation in chromosomally abnormal
villi.
READING LIST 32 2001
1. World Health Organization classification
of neoplastic diseases of the hematopoietic and lymphoid tissues:
a progress report
2. World Health Organization classification of neoplastic diseases
of the hematopoietic and lymphoid tissues: report of the clinical
advisory committee
READING LIST 33 2001
1. FISH identifies inv(16)(p14q22)
masked by translocations in three cases of acute myeloid leukemia
2. t(11;14)-positive mantle cell lymphomas exhibit complex karyotypes
and share similarities with B-cell chronic lymphocytic leukemia
3. Isodicentric 7p, idic(7)(q11.3), in acute myeloid leukemia
associated with older age and favorable response to induction
chemotherapy: a new clinical entity?
READING LIST 34 2001
1. Comparative Genomic Hybridization
in Combination with Flow Cytometry Improves Results of Cytogenetic
Analysis of Spontaneous Abortions
2. Comparative Genomic Hybridization: A New Approach to Screening
for Intrauterine Complete or Mosaic Aneuploidy
3. Limitations of Chromosome Classification by Multicolor Karyotyping
READING LIST 35 2001
1. Prenatal Diagnosis of Mosaic
Trisomy 8 with Investigations of the Extent and Origin of Trisomic
Cells
2. Genetics of Beckwith-Wiedemann Syndrome Associated Tumors:
Common Genetic Pathways
3. Velo-cardio-Facial Syndrome: A Distinctive Behavioral Phenotype
READING LIST 36 - 2002
1. Identification of Uniparental
Disomy Following prenatal Detection of Robertsonian Translocations
and Isochromosomes.
2. Prenatal Diagnosis using interphase Fluorescence in situ
Hybridiation (FISH): 2 year Multi-Center Retrospective Study
and Review of the Literature
3. Preimplantation Genetic diagnosis of Pericentric Inversions
READING LIST #37 - 2002
1. Pharmacogenetics
2. Consent and Privacy in Pharmacogenetic Testing
3. Genetic Information, Genomic Technologies, and the Future
of Drug Discovery
4. Mapping a Role for SNP's in Drug Development
READING LIST 38 2002
1. Double Minute Chromosomes in Acute Myeloid Leukemia and Myelodysplastic
Syndrome: Identification of New Amplification Regions by Fluorescence
In Situ Hybridization and Spectral Karyotyping
2. Common Fragile Sites Associated with the Breakpoints of Chromosomal
Aberrations in Hematologic Neoplasms
3. High Frequency of Leukemic Clones in Newborn Screening Blood
Samples of Children with B-precursor Acute Lymphoblastic Leukemia
READING LIST 39 2002
1. Prediction by FISH Analysis of the Occurrence of Wilms Tumor
in Aniridia Patients
2. Comprehensive Karyotyping of the HT-29 Colon Adenocarcinoma
Cell Line
3. Cytogenetic Clues to Breast Carcinogenesis
READING LIST 40
2002
1. From Chromosomal Alterations to Target Genes for Therapy:
Integrating Cytogenetics and Functional Genomic Views of the
Breast Cancer Genome
2. High-throughput Genomic and Proteomic Analysis Using Microarray
Technology
3. DNA Analysis in a Paternity Case Involving a Triploid Fetus
Note: Availability of articles on-line
does not imply the service is free. Some journals require a subscription
or impose a fee. The web
addresses are included for the convenience of those wishing to
obtain the articles in this way.
Copy right law prohibits AGT from supplying
readers with the actual journal articles (electronically or otherwise).
Journal Club order forms are available
in the Journal of the Association of Genetic Technologists, GeneTalk
or by contacting the AGT Executive Office at agt-info@goAMP.com.
This list is current as of
9/1/2002.
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