Abgc boards overview - Study guides, Class notes & Summaries
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ABGC Boards Overview – Questions With A+ Solutions
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ABGC Boards Overview Questions and Answers 100% Solved
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ABGC Boards Overview Questions 
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Angelman Syndrome causes (expression and % of total) ️️**paternal imprinting defect, 
should be maternal expression 
5-7 kb deletion on maternal chr15q11.2-13 (60-70%) 
UBE3A maternal deletion (11%) 
Paternal UPD15 (3-7%) 
Angelman testing strategy and condition features ️️methylation first since finds ~80% of 
cases then UBE3A seq and del/dup 
features: happy demeanor, abnormal gait, seizures, delayed/absent speech 
Prader-Wil...
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ABGC Boards - Genetics Overview (Penn - GENC 601 Exam 1 & 2, GENC 613 Exam 1) – Qs & As
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ABGC Boards - Genetics Overview (Penn - GENC 601 Exam 1 & 2, GENC 613 Exam 1) – Qs & As
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ABGC Boards Overview Study Guide Exam Questions and Answers
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ABGC Boards Overview Study Guide 
Exam Questions and Answers 
Angelman Syndrome causes (expression and % of total) - CORRECT ANSWER- 
**paternal imprinting defect, should be maternal expression 
5-7 kb deletion on maternal chr15q11.2-13 (60-70%) 
UBE3A maternal deletion (11%) 
Paternal UPD15 (3-7%) 
Angelman testing strategy and condition features - CORRECT ANSWER-methylation 
first since finds ~80% of cases then UBE3A seq and del/dup 
features: happy demeanor, abnormal gait, seizures, delaye...
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ABGC Boards Overview Exam With 100% Correct And Verified Answers 2024
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ABGC Boards Overview Exam With 100% Correct And Verified Answers 2024
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ABGC Boards Bundled Exams with Complete Solutions 100% Verified by Experts
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ABGC Boards: Metabolic Exam Questions and Answers 100% Solved

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ABGC 100 disorders Exam with Correct Answers 100% Solved

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ABGC Board Study Genes Questions and Answers 100% Solved

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ABGC Boards - Final Review Questions and Answers 100% Solved

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ABGC Boards Overview
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ABGC Boards Overview Questions and Answers
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ABGC Boards Overview 
 
Angelman Syndrome causes (expression and % of total) - Answer-**paternal imprinting defect, should be maternal expression 
 
5-7 kb deletion on maternal chr15q11.2-13 (60-70%) 
UBE3A maternal deletion (11%) 
Paternal UPD15 (3-7%) 
 
Angelman testing strategy and condition features - Answer-methylation first since finds ~80% of cases then UBE3A seq and del/dup 
 
features: happy demeanor, abnormal gait, seizures, delayed/absent speech 
 
Prader-Willi Syndrome causes (expr...
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