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Showing 1 to 12 of 33 entries
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Direct effect of preferential segregation on the origin of polysomy.


PMID: 13418767
Nature. 1957 Mar 30;179(4561):683. doi: 10.1038/179683a0.

No abstract available.

Routine genetic testing for Asperger syndrome.

Genetics in medicine : official journal of the American College of Medical Genetics

Chodirker BN, Chudley AE.
PMID: 18941416
Genet Med. 2008 Nov;10(11):843-5; author reply 845. doi: 10.1097/GIM.0b013e31818b0c76.

No abstract available.

What do cytogenetic abnormalities after autotransplant really mean?.

Biology of blood and marrow transplantation : journal of the American Society for Blood and Marrow Transplantation

Rossi G, Gale RP.
PMID: 25128616
Biol Blood Marrow Transplant. 2014 Nov;20(11):1870-1. doi: 10.1016/j.bbmt.2014.08.006. Epub 2014 Aug 14.

No abstract available.

Cytogenetic analysis of tumor clonality.

Advances in cancer research

Teixeira MR, Heim S.
PMID: 21925303
Adv Cancer Res. 2011;112:127-49. doi: 10.1016/B978-0-12-387688-1.00005-3.

All or almost all neoplasias subjected to systematic cytogenetic scrutiny have been found to harbor acquired chromosomal aberrations. The paradigm stemming from the study of hematopoietic malignancies and sarcomas is that cancers are of monoclonal origin (i.e., they have...

Evaluation of non-invasive prenatal testing to detect chromosomal aberrations in a Chinese cohort.

Journal of cellular and molecular medicine

Cui W, Liu X, Zhang Y, Wang Y, Chu G, He R, Zhao Y.
PMID: 31454164
J Cell Mol Med. 2019 Nov;23(11):7873-7878. doi: 10.1111/jcmm.14614. Epub 2019 Aug 27.

The aim of this study was to evaluate the clinical feasibility of non-invasive prenatal testing (NIPT) to detect foetal copy number variations (CNVs). Next-generation sequencing for detecting foetal copy number variations (CNVs) was performed on the collected samples from...

[Application of single nucleotide polymorphism microarray in clinical diagnosis of intellectual disability or retardation].

Zhejiang da xue xue bao. Yi xue ban = Journal of Zhejiang University. Medical sciences

Hu J, Qian Y, Sun Y, Yu J, Luo Y, Dong M.
PMID: 31901047
Zhejiang Da Xue Xue Bao Yi Xue Ban. 2019 Jun 25;48(4):420-428.

OBJECTIVE: To assess the clinical application of single nucleotide polymorphism microarray (SNP array) in patients with intellectual disability/developmental delay(ID/DD).METHODS: SNP array was performed to detect genome-wide DNA copy number variants (CNVs) for 145 patients with ID/DD in Women's Hospital,...

Adaptive classifiers for dicentric chromosomes.

Journal of radiation research

Piper J, Sprey J.
PMID: 1507167
J Radiat Res. 1992 Mar;33:159-70. doi: 10.1269/jrr.33.supplement_159.
Free Article

Classification of dicentric chromosomes in a practical automatic screening system comprises three stages. The first generates plausible centromere candidates from each chromosome in an automatically segmented metaphase, and uses contextual knowledge to generate distributions of "probably true" and "probably...

Cytogenetic abnormalities in lung cancer.

Cancer treatment and research

Campbell L, Brown J, Garson OM, Morstyn G.
PMID: 2577168
Cancer Treat Res. 1989;45:123-36. doi: 10.1007/978-1-4613-1593-3_8.

No abstract available.

Monitoring of genetic instability in subjects with increased risk of cancer.

Annali dell'Istituto superiore di sanita

Nuzzo F, Stefanini M.
PMID: 2751199
Ann Ist Super Sanita. 1989;25(1):81-9.

Results of investigations performed to obtain data on genomic instability in subjects with increased risk of cancer are reported. People at risk for environmental or genetic factors included in this study were: 1) individuals from the Seveso population exposed...

Letter: Do only a few chromosomes carry genes of prime importance for malignant transformation?.

Lancet (London, England)

Mitelman F, Levan G.
PMID: 59288
Lancet. 1976 Jul 31;2(7979):264. doi: 10.1016/s0140-6736(76)91076-x.

No abstract available.

On the localization of genes on certain autosomes of man through chromosome aberrations. 3. Exclusion of the possibility of gene assignment.


Bender K, Burckhardt K.
PMID: 5488998
Humangenetik. 1970;9(1):75-85. doi: 10.1007/BF00696016.

No abstract available.


Genetic counseling (Geneva, Switzerland)

Rivera H.
PMID: 27192897
Genet Couns. 2016;27(1):91-3.

No abstract available.

Showing 1 to 12 of 33 entries