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TAR syndrome
Thrombocytopenia-Absent Radius Syndrome
TAR Syndrome, a Rare Case Report with Cleft Lip/Palate a Naseh, a Hafizi, F Malek, H Mozdarani, V Yassaee
(TAR) Syndrome Without Significant Thrombocytopenia
1Q21.1 Deletion and a Rare Functional Polymorphism in Siblings with Thrombocytopenia-Absent Radius–Like Phenotypes
Soonerstart Automatic Qualifying Syndromes and Conditions
Cytogenetics
Thrombocytopenia-Absent Radius (TAR) Syndrome Service At
Absent Radius (TAR) Syndrome
Chromosomal Microarray, Postnatal, Clarisure® Oligo-SNP
Appendix 8: Approved Established Risk Conditions for Babynet
An Interesting Case of Phocomelia
Prenatal Detection of TAR Syndrome in a Fetus with Compound Inheritance of an RBM8A SNP and a 334‑Kb Deletion: a Case Report
A Child with Radius Aplasia, Cleft of Lip and Palate, Microcephaly, and Unusual Chromosome Findings
Neonatal Thrombocytopenia: Causes and Management I Roberts, N a Murray
EUROCAT Syndrome Guide
(Arteriohepatic Dysplasia) Syndrome Peripheral
Rare Syndrome of Thrombocytopenia Absent Radius Diagnosed Prenatally in a Female Fetus Case Report Abstract Imedpub Journals
Beyond Gmezlpezhernndez Syndrome: Recurring Phenotypic
Top View
Prenatal Diagnosis and Post-Mortem Examination
Chromosome 1
Congenital Anomalies Surveillance 2013-2014
Syndrome of the Month Thrombocytopenia and Absent Radius
1 Chromosome Chapter
Original Article
Supplement Nr. 18 | 2018 Anästhesiologie
10P13 DELETION
Advances in Genetic Studies of Inherited Bone Marrow Failure Syndromes and Their Associated Malignancies
Bone Marrow Morphology and Disease Progression in Congenital
Thrombocytopenia-Absent Radius Syndrome
Intracranial Hemorrhage in Newborn with TAR Syndrome—A Feared Complication
1Q21.1 Microdeletion
A Three-Step Workflow Procedure for the Interpretation of Array-Based
Acute Myeloid Leukemia in a Patient with Thrombocytopenia with Absent Radii: a Case Report and Review of the Literature
REVIEW the Genetics of Familial Leukemia M Horwitz
EUROCAT Guide 6: Definition and Coding of Syndromes
10P13 DELETION
Proximal Microdeletions and Microduplications of 1Q21.1 Contribute to Variable Abnormal Phenotypes
Thrombocytopenia-Absent Radius Syndrome
(TAR) Syndrome Mohammad Manna Al-Qattan
Complex Genetics of Radial Ray Deficiencies: Screening of a Cohort of 54 Patients
Inherited Platelet Disorders: an Updated Overview
Next Generation Sequencing Panel for Hereditary Myeloid Malignancy and Inherited Bone Marrow Failure
Laboratory Diagnostics of Inherited Platelet Disorders
Myeloid Neoplasms with Germline Predispositions New Recognition in the Revised WHO Classification
The Genetics of Microdeletion and Microduplication Syndromes: an Update
When Should Congenital Inherited Thrombocytopenia Be Suspected?
Soonerstart Automatic Qualifying Syndromes and Conditions
Management of Inherited Thrombocytopenia Recommendations of the Group on Hemostasis of the Polish Society of Hematology and Transfusion Medicine, 2019
1Q21.1 Microdeletions
A Case of TAR Syndrome (Trombocytopenia with Absent Radius Syndrome)
Two Patterns of Thrombopoietin Signaling Suggest No Coupling Between Platelet Production and Thrombopoietin Reactivity in Thrombocytopenia-Absent Radii Syndrome
58 Days Old Infant TAR SYNDROME with COVID-19 Infection
Chromosome Abnormalities Reference
Occurrence of Radial Club Hand in Children with Different Syndromes