DOCSLIB.ORG
Explore
Sign Up
Log In
Upload
Search
Home
» Tags
» Monosomy 9p
Monosomy 9p
Abstracts from the 50Th European Society of Human Genetics Conference: Electronic Posters
Detailed Characterization Of, and Clinical Correlations In, 10 Patients
Sexual Dimorphism in Diverse Metazoans Is Regulated by a Novel Class of Intertwined Zinc Fingers
Early ACCESS Diagnosed Conditions List
2003 Birmingham
Association of Distal Deletion of the Short Arm of Chromosome 9 with 46
S2 Table. Genetic Syndromes Displaying Various Craniofacial Abnormalities, Used to Locate Candidate Genes for the Study
Study of 250 Children with Idiopathic Mental Retardation Reveals Nine Cryptic and Diverse Subtelomeric Chromosome Anomalies
Mosaic Tetrasomy 9P Case with the Phenotype Mimicking Klinefelter Syndrome and Hyporesponse of Gonadotropin-Stimulated Testosterone Production
NIFTYTM Plus
Chromosomal Microarray Chromosomal Microarray
FISH Mapping of the Sex-Reversal Region on Human Chromosome 9P in Two XY Females and in Primates
Code Disease Name
De Novo Terminal Deletion 7P22.1 Pter in a Child Without
Familial Translocation T(9;16)
Co-Existing 9P Duplication & Deletion
Using Balanced Translocation to Discover Novel Disease Causing Genes
A De Novo Marker Chromosome Derived from 9P in a Patient with 9P
Top View
Clinical Report
Chromosome Breakage Hotspots and Delineation of the Critical Region for the 9P-Deletion Syndrome Laurie A
9P Partial Monosomy and Disorders of Sex Development: Review and Postulation of a Pathogenetic Mechanism Shane C
(19) United States (12) Patent Application Publication (10) Pub
Disorders of Sex Development—Novel Regulators, Impacts on Fertility, and Options for Fertility Preservation
WO 2013/109981 Al O
Cryptic 7Q21 and 9P23 Deletions in a Patient with Apparently
PRENATAL DETECTION of a FAMILIAL Der(18)
Therapeutic and Diagnostic Agents
Type 1 Established Condition List
From 80 Cases
Clefting in Trisomy 9P Patients: Genotype-Phenotype Correlation Using Microarray Comparative Genomic Hybridization
Cytogenomic Characterization of an Unexpected 17.6Mb 9P Deletion Associated to a 14.8Mb 20P Duplication in a Dysmorphic Patient
(12) Patent Application Publication (10) Pub. No.: US 2010/0138165 A1 Fan Et Al
We Recently Encountered a Case of Develop
Partial Trisomy 9P22 to 9P24.2 in Combination with Partial Monosomy 9Pter in a Syrian Girl Walid Al Achkar1*, Abdulsamad Wafa1, Faten Moassass1, Thomas Liehr2
Prevalence and Incidence of Rare Diseases
Genetics Studies. He Was the First Baby Born to a Non- Interstitial Deletions of Chromosome 13 Are Known to Consanguineous Couple
Familial Balanced Translocation Leading to an Offspring with Phenotypic Manifestations of 9P Syndrome
Maternal Translocation (9;18) with Two Abnormal Offspring Each With
Non-Invasive Prenatal Testing
Chromosome Abnormalities Reference
Partial Deletion of DMRT1 Causes 46,XY Ovotesticular Disorder Of
Fetal Dna Chip Detection List 20160511