Department of Molecular and Human Genetics

Clinical Biochemical Genetics Fellowship

Master
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Training in Clinical Biochemical Genetics

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Trainees in Clinical Biochemical Genetics spend three months learning each of the following methods: tandem mass spectrometry; gas chromatography/mass spectrometry; high-pressure liquid chromatography (amino acid analysis) and enzyme analysis in the Biochemical Genetics Laboratory.

Each day, the trainee participates in writing interpretations for all tests with one of the laboratory directors. The remainder of the training is spent developing new diagnostic tests or methodologies for the laboratory or working on a research project.

The Biochemical Genetics Laboratory was established more than 25 years ago and has been a leader in the diagnosis of inborn errors of metabolism. The laboratory analyzes over 8,000 clinical samples per year as well as providing contract service for research. In addition to standard biochemical genetics testing, the laboratory was the first laboratory in the United States to offer large scale metabolomics profiling to screen for inborn errors of metabolism.

Laboratory Director: Sarah Elsea, Ph.D.

Medical Director: V. Reid Sutton, M.D.

View information on how to apply for this training program.

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Year 1: Clinical Biochemical Genetics

Months

Rotation

July - Sept.

Amino Acids (HPLC)

Oct. - Dec.

Organic Acids (GC/MS)

Jan. -March

Acylcarnitines (MS/MS)

April-June

Mitochondrial

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Year 2: Clinical Biochemical Genetics

Months

Rotation

July - Sept.

Enzymes

Oct. - Nov.

TCH Clinic

Dec. - June

Research/New Test Development

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Conferences

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Trainees are required to attend a series of regularly-scheduled conferences, seminars and lectures.

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Apply To Program

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View information on how to apply to the Clinical Laboratory Fellowship Training Program

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