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Uniparental disomy
Robertsonian Translocations FTNW
Sema4 Noninvasive Prenatal Select
Fragile X Syndrome
Inheriting Genetic Conditions
Mosaic Genome-Wide Maternal Isodiploidy: an Extreme Form Of
Risk Estimation of Uniparental Disomy of Chromosome 14 Or 15 in a Fetus with a Parent Carrying a Non-Homologous Robertsonian Translocation
PRENATAL DIAGNOSIS of PATERNAL UNIPARENTAL ISODISOMY of CHROMOSOME 14 (Patiupd14) with CHROMOSOMAL MICRO-ARRAY in a FETUS with MULTIPLE CONGENITAL ABNORMALITIES
Copy-Neutral Loss of Heterozygosity and Chromosome Gains and Losses
Maternal Uniparental Disomy of Chromosome 20 (UPD(20)Mat) As Differential Diagnosis of Silver Russell Syndrome: Identification of Three New Cases
Chromosomal Disorders
Frequent Occurrence of Uniparental Disomy in Colorectal Cancer
Uniparental Disomy (UPD)
A Search for Uniparental Disomy in Carriers of Supernumerary Marker
Identification of Paternal Uniparental Disomy on Chromosome 22 and A
Diagnostic Testing for Uniparental Disomy: a Points to Consider Statement from the American College of Medical Genetics and Genomics (ACMG)
A Placental Diploid Cell Line Is Not Essential for Ongoing Trisomy 13 Or
And Uniparental Disomy (UPD): Coincidence Or Consequence? D Kotzot
Syndrome of the Month
Top View
Sex Linked Diseases
General Information About Positive NIPT Results
Chromosomal Abnormalities and Mental Illness
Incidence of X and Y Chromosomal Aneuploidy in a Large Child Bearing Population
Patterns and Frequencies of Acquired and Constitutional Uniparental Isodisomies in Pediatric and Adult B-Cell Precursor Acute Lymphoblastic Leukemia
Uniparental Disomy
Uniparental Disomy (UPD) Tech Review.Indd
Molecular Allelokaryotyping of Relapsed Pediatric Acute Lymphoblastic Leukemia
Low Incidence of UPD in Spontaneous Abortions Beyond the 5Th Gestational Week
Paternal Uniparental Disomy of Chromosome 14 and Unique Exchange of Chromosome 7 in Cases of Spontaneous Abortion
Chromosomal Mosaicism and Uniparental Disomy in Prenatal Diagnosis: Clinical Implications for Genetic Counseling
Methylation Analysis (Of Chromosomes 14 and 15)
Applications of Genome Editing Technology in Research on Chromosome Aneuploidy Disorders
Cytogenetics Into Cytogenomics: SNP Arrays Expand the Screening Capabilities of Genetics Laboratories Contributed by Laura K
Non-Mendelian Inheritance
Letter Advance Publication DOI: 10.5582/Irdr.2016.01043
Mosaicism for Trisomy 21: a Review
Clinical Relevance of Screening for Rare Autosomal Aneuploidies: a Case of Maternal Uniparental Disomy J