Our review is designed to help you maximize your score on the Molecular-Genetic Exam. StatPearls questions and articles are linked directly to American Board of Pathology® content outlines. Each review course is designed to empower you to assess your knowledge and understanding of medical principles and concepts found on the Molecular-Genetic Exam.
We have 421 Multiple-choice 1st, 2nd, and 3rd order questions with four detailed teaching points linked to 334 PubMed indexed review articles related to the Molecular-Genetic Examination . You can customize practice questions to anatomical and clinical Pathologic Genetics Specialist subject areas. In addition, you will have access to a 250 question pre- and post-test Molecular-Genetic Exam to help you target learning and identify areas that need further study. Analytics and reports allow you to compare your scores to other students.
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The StatPearls molecular genetic prep questions, molecular genetic review questions, and molecular genetic test questions will help you achieve a top score on the Molecular-Genetic Examination . 364 authors and 10 editors have contributed to the development of the Molecular-Genetic Exam content, which is continuously refined and updated to improve your learning experience.
Molecular-Genetic Exam Overview
How many hours is the Molecular-Genetic Exam?
The Molecular-Genetic Exam is 7 hours.
How many questions is the Molecular-Genetic Exam?
The Molecular-Genetic Exam is 270 questions.
What topics are covered on the Molecular-Genetic Exam?
Topics include: Normal Structure and Function - 9%, Molecular Genetic Principles - 6%, Techniques and Methods - 3%, Assay Performance and Validation - 6%, Quality - 6%, Ethical, Legal, and Regulatory Issues - 6%, Indications for Testing - 6%, Inherited Diseases - 10%, Inherited Cancer Syndromes - 3%, Solid Tumors - 9%, Hematopathology - 8%, Pharmacogenetics - 4%, Infectious Diseases - 8%, Identity Testing - 4%, Histocompatibility - 1%, Informatics - 3%, and Laboratory Management-General - 8%
Molecular-Genetic Exam MCQs (421)
Our question bank for the Molecular-Genetic Exam covers four Cognitive Difficulty Levels:
- Allergy and Immunology - 16 questions
- Cardiovascular - 17 questions
- Connective Tissue - 11 questions
- Ears Nose and Throat - 15 questions
- Endocrine and Metabolic - 70 questions
- Eyes - 12 questions
- Gastrointestinal - 32 questions
- Genetics - 334 questions
- Genitourinary - 13 questions
- Growth and Development - 83 questions
- Gynecologic - 19 questions
- Hematologic - 59 questions
- Infectious - 21 questions
- Integument - 59 questions
- Musculoskeletal - 47 questions
- Nervous - 65 questions
- Obstetric - 7 questions
- Oncologic - 159 questions
- Psychiatric Mental Health - 4 questions
- Pulmonary - 19 questions
- Renal - 19 questions
- Surgery - 4 questions
- Toxicology - 3 questions
- Manage Care and Comply Regulations - 2 questions
- Health Promotion & Maintenance (Prevent Problems) - 3 questions
- Pharm/Parenteral Therapy (Drugs/Vital Signs) - 11 questions
- Physiological Adaptation (Care Ill Patients) - 256 questions
- Process (Analysis, Assess, Eval, Implement, Plan) - 272 questions
- Teaching/Learning (Promotes Behavior Change) - 1 questions
- Causes - 218 questions
- Classification - 42 questions
- Differential - 276 questions
- Epidemiology - 15 questions
- Evaluation Diagnostic Tests - 227 questions
- Evaluation Lab - 219 questions
- Evaluation Monitoring - 9 questions
- Evaluation Nuclear Medicine - 2 questions
- Evaluation Procedures - 100 questions
- Evaluation Radiologic - 67 questions
- Health Maint Prevention Public Health - 2 questions
- History Physical - 409 questions
- Pathophysiology - 359 questions
- Patient Education - 3 questions
- Prognosis Complications - 252 questions
- Toxicology - 3 questions
- Treatment Medical - 24 questions
- Treatment Radiation - 1 questions
- Treatment Surgical - 12 questions
- Clinical Education - 3 questions
- Therapeutics (Drug treatment) - 4 questions
- Drug Information - 5 questions
- Pharmaceutics (Safely dosing medications) - 4 questions
- Pharmacokinetics (Drug movement in body) - 1 questions
Molecular-Genetic Exam Articles (334)
The most common type of cancer arising in the kidney is renal cell carcinoma (aka hypernephroma or Grawitz tumor), making up more than 9 out of 10 ...
is a genus belonging to the family of Enterobacteriaceae that is associated primarily with healthcare-related ...
"Atypical glandular cells (AGC)" is the term adopted by The Bethesda system of reporting cervicovaginal cytology.
The “sports physical,” otherwise referred to as “preparticipation physical evaluation” is the result of a collaborative eff ...
Sweat glands are appendages of the integument. There are eccrine and apocrine sweat glands. They differ in embryology, distribution, and ...
Congenital myotonic dystrophy (CMD) is an autosomal dominant genetic disorder caused by trinucleotide repeat expansion of CTG (cytosine-thymine-gua ...
Nevus flammeus or port-wine stain is a capillary malformation presenting as a pink or red patch on a newborn's skin. It is a congenital skin condit ...
The dentate nucleus is the largest deep cerebellar cluster of neurons; it has a dentated – serrated – edge. Efferent fibers of the dent ...
Agammaglobulinemia or hypogammaglobulinemia is a rare inherited immunodeficiency disorder. It is characterized by low or absent mature B cells, whi ...
According to the Surveillance, Epidemiology, and End Results (SEER) Program, vulvar cancer represents 0.3% of all new cancer cases annually at ...
Cornelia de Lange syndrome (CdLS) was described, in 1933, by the Dutch pediatrician, Cornelia Catharina de Lange, who illustrated two unrelate ...
Angioneurotic edema is a relatively common presentation in the emergency department (ED). It presents as unpredictable frequent edematous ...
Glycogen storage disease type II (GSD2, Pompe Disease) is a recessive metabolic disorder, creating glycogen deposits inside lysosomes within the mu ...
Aplasia cutis congenita (ACC) is a rare congenital skin defect characterized by a focal or extensive absence of the epidermis, dermis, an ...
Congenital poikiloderma, also known as Rothmund-Thomson syndrome (RTS), is a rare genodermatosis of autosomal recessive (AR) inheritance characteri ...
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