Recent Publications on Karyotyping: |  |
A Prospective Study on the Effect of Rapid Aneuploidy Testing (Amnio-PCR) on Anxiety Levels and Quality of Life Measures in Women and Their Partners with Positive Down Screening Result.
Objectives: To examine the effect of rapid aneuploidy testing by amnio-PCR...
Direct Link | 30th August, 2008
| Department of Obstetrics and Gynaecology, Kwong Wah Hospital, Hong Kong
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Clinical findings in prepubertal girls with inguinal hernia with special reference to the diagnosis of androgen insensitivity syndrome.
Objective. Complete androgen insensitivity syndrome (CAIS) is a rare...
Direct Link | 30th August, 2008
| Department of Paediatric Surgery, University Hospital, Turku, Finland.
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| Loss of the Y chromosome: an age-related or clonal phenomenon in acute myelogenous leukemia/myelodysplastic syndrome?
| 30th August, 2008
| Department of Pathology, Cedars-Sinai Medical Center, Los Angeles, CA
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| [The guideline 'Recurrent miscarriage' (first revision) of the Dutch Society for Obstetrics and Gynaecology]
| 22nd August, 2008
| Academisch Medisch Centrum/Universiteit van Amsterdam, afd. Verloskunde en
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| The histopathology of a human mesenchymal stem cell experimental tumor model: support for an hMSC origin for Ewing's sarcoma?
| 21st August, 2008
| Department of Endocrinology and Metabolism, Odense University Hospital,
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CGcgh: a tool for molecular karyotyping using DNA microarray-based comparative genomic hybridization (array-CGH).
Microarray-based comparative genomic hybridization (array-CGH) is a...
Direct Link | 21st August, 2008
| Genomic Medicine Research Core Laboratory, Chang Gung Memorial Hospital,
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Prenatal diagnosis of chromosomal abnormalities in a resource-poor setting.
OBJECTIVE: To compare the efficacy and efficiency of systematic,...
Direct Link | 19th August, 2008
| Department of Obstetrics and Gynecology, Tygerberg Hospital, University of
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The impact of trisomy 12, retinoblastoma gene and P53 in prognosis of B-cell chronic lymphocytic leukemia.
PURPOSE: Routine cytogenetic analysis frequently fails to identify an...
Direct Link | 16th August, 2008
| Clinical Oncology Center, Cairo University Hospital, Cairo University,
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A 10.7 Mb interstitial deletion of 13q21 without phenotypic effect defines a further non-pathogenic euchromatic variant.
Chromosome 13 deletions are associated with widely varying phenotypes but...
Direct Link | 14th August, 2008
| Institute of Human Genetics, RWTH Aachen, Aachen, Germany.
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| Holoprosencephaly: an antenally-diagnosed case series and subject review.
| 13th August, 2008
| Cytogenetics Laboratory, Department of Pathology, Singapore General
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A case-control study identifying chromosomal polymorphic variations as forms of epigenetic alterations associated with the infertility phenotype.
OBJECTIVE: To study the association of chromosomal polymorphic variations...
Direct Link | 12th August, 2008
| Department of Assisted Reproduction and Genetics, Jaslok Hospital and
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Cytogenetic, molecular genetic, and clinical characteristics of acute myeloid leukemia with a complex karyotype.
Patients with acute myeloid leukemia (AML) harboring three or more...
Direct Link | 12th August, 2008
| Division of Hematology and Oncology, Department of Internal Medicine,
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Detection of cryptic subtelomeric imbalances in fetuses with ultrasound abnormalities.
It is known from postnatal diagnosis that imbalances of the subtelomeric...
Direct Link | 12th August, 2008
| Department of Human Genetics, Radboud University Nijmegen Medical Center,
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Prenatal detection of trisomy 21 by second-trimester ultrasound examination and maternal age in a non-selected population of 49 314 births in Norway.
OBJECTIVES: To assess the contribution of the second-trimester routine...
Direct Link | 9th August, 2008
| National Center for Fetal Medicine, Women and Children's Center, St Olavs
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| [A case of acute promyelocytic leukemia with variant t(5;17) and trisomy 22.]
| 7th August, 2008
| Department of Hematology, the First Affiliated Hospital, Nanjing Medical
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