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- Genomic Designation: New Kinds of People at the Intersection of Genetics, Medicine and Social Action
- P-00814 (12/2020) 4
- Optical Genome Mapping As a Next-Generation Cytogenomic Tool for Detection of Structural and Copy Number Variations for Prenatal Genomic Analyses
- Complex Ssmc Involving X and Y Chromosomes in Two Patients With
- Emanuel Syndrome: First Case Reported in Mexico Investigación Clínica, Vol
- Non-Invasive Prenatal Screening for Emanuel Syndrome Yuqin Luo1,2, Jie Lin2, Yixi Sun1,2, Yeqing Qian1,2, Liya Wang1,2, Min Chen1,2, Minyue Dong1,2 and Fan Jin1,2,3*
- Anesthetic Management for Tethered Cord Syndrome in a Child with Emanuel Syndrome
- The Constitutional Balanced Translocation T(11;22)(Q23;Q11.2)-An Indian Account
- Cytogenetics Lecture 1: Introduction to Clinical Cytogenetics
- Clinical Vignette Abstracts NASPGHAN 2017
- Diagnosis and Management of Genetic Derivation 22 and 11 Chromosome-Emanuel Syndrome in 10-Year Old Boy
- Southern Regional Meeting
- Global Journal of Medical Research: F Diseases Cancer, Ophthalmology & Pediatric
- CD OCD Vol 2 2015-20 Plan 05-05-15
- 57 Abstracts
- Phenotypic Characterization of Derivative 22 Syndrome: Case Series and Review
- Emanuel Syndrome
- Emanuel Syndrome (Es): New Case-Report and Review of the Literature
- (Emanuel) Syndrome: a Case Report and a Review
- Supernumerary Derivative (22) Syndrome Resulting from a Maternal Balanced Translocation Afroze B, Ngu L H, Roziana A, Aminah M, Noor Shahizan A
- Systems Bioinformatics
- Emanuel Syndrome: First Case Reported in Mexico
- Making a Genetic Diagnosis in a Level IV Neonatal Intensive Care Unit Population
- A Clinical and Molecular Analysis of a Patient with Emanuel Syndrome