Maternal age and chromosomally abnormal pregnancies: what we know and what we wish we knew
T Hassold, P Hunt - Current opinion in pediatrics, 2009 - journals.lww.com
Maternal age and chromosomally abnormal pregnancies: what we... : Current Opinion in
Pediatrics Maternal age and chromosomally abnormal pregnancies: what we know and what we …
Pediatrics Maternal age and chromosomally abnormal pregnancies: what we know and what we …
Forensic typing of short tandem repeat markers on the X and Y chromosomes
TM Diegoli - Forensic Science International: Genetics, 2015 - Elsevier
Short tandem repeat (STR) markers are the cornerstone of forensic identity and kinship
testing. Markers located on the X and the Y chromosome can complement those found on …
testing. Markers located on the X and the Y chromosome can complement those found on …
A general approach for haplotype phasing across the full spectrum of relatedness
Many existing cohorts contain a range of relatedness between genotyped individuals, either
by design or by chance. Haplotype estimation in such cohorts is a central step in many …
by design or by chance. Haplotype estimation in such cohorts is a central step in many …
The landscape of recombination in African Americans
Recombination, together with mutation, gives rise to genetic variation in populations. Here
we leverage the recent mixture of people of African and European ancestry in the Americas …
we leverage the recent mixture of people of African and European ancestry in the Americas …
[图书][B] Handbook of human genetic linkage
JD Terwilliger, J Ott - 1994 - books.google.com
In his book Analysis of Human Genetic Linkage Jurg Ott laid out the principles by which
geneticists perform studies of genetic linkage in humans. Here, in the Handbook of Human …
geneticists perform studies of genetic linkage in humans. Here, in the Handbook of Human …
Genome-Wide Crossover Distribution in Arabidopsis thaliana Meiosis Reveals Sex-Specific Patterns along Chromosomes
L Giraut, M Falque, J Drouaud, L Pereira… - PLoS …, 2011 - journals.plos.org
In most species, crossovers (COs) are essential for the accurate segregation of homologous
chromosomes at the first meiotic division. Their number and location are tightly regulated …
chromosomes at the first meiotic division. Their number and location are tightly regulated …
Meta-analysis of 32 genome-wide linkage studies of schizophrenia
MYM Ng, DF Levinson, SV Faraone, BK Suárez… - Molecular …, 2009 - nature.com
A genome scan meta-a nalysis (GSMA) was carried out on 32 independent genome-wide
linkage scan analyses that included 3255 pedigrees with 7413 genotyped cases affected …
linkage scan analyses that included 3255 pedigrees with 7413 genotyped cases affected …
SNPs for a universal individual identification panel
AJ Pakstis, WC Speed, R Fang, FCL Hyland… - Human genetics, 2010 - Springer
An efficient method to uniquely identify every individual would have value in quality control
and sample tracking of large collections of cell lines or DNA as is now often the case with …
and sample tracking of large collections of cell lines or DNA as is now often the case with …
A high-density SNP-based linkage map of the chicken genome reveals sequence features correlated with recombination rate
MAM Groenen, P Wahlberg, M Foglio… - Genome …, 2009 - genome.cshlp.org
The resolution of the chicken consensus linkage map has been dramatically improved in this
study by genotyping 12,945 single nucleotide polymorphisms (SNPs) on three existing …
study by genotyping 12,945 single nucleotide polymorphisms (SNPs) on three existing …
[HTML][HTML] The FORCE panel: an all-in-one SNP marker set for confirming investigative genetic genealogy leads and for general forensic applications
A Tillmar, K Sturk-Andreaggi, J Daniels-Higginbotham… - Genes, 2021 - mdpi.com
The FORensic Capture Enrichment (FORCE) panel is an all-in-one SNP panel for forensic
applications. This panel of 5422 markers encompasses common, forensically relevant SNPs …
applications. This panel of 5422 markers encompasses common, forensically relevant SNPs …
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