Medical genetics and genomic medicine in the United States of America. Part 1: history, demographics, legislation, and burden of disease

Author:

Ferreira Carlos R.12ORCID,Regier Debra S.2,Hadley Donald W.1,Hart P. Suzanne1,Muenke Maximilian1

Affiliation:

1. National Human Genome Research Institute; National Institutes of Health; Bethesda Maryland

2. Rare Disease Institute; Children's National Health System; Washington District of Columbia

Publisher

Wiley

Subject

Genetics (clinical),Genetics,Molecular Biology

Reference101 articles.

1. Dysmorphogenesis of joints, brain, and palate: a new dominantly inherited syndrome;Aase;J. Pediatr.,1968

2. Hereditary deformities in man due to arrested development;Adams;J. Hered.,1945

3. Syndrome characterized by osteitis fibrosa disseminata, areas of pigmentation and endocrine dysfunction, with precocious puberty in females: report of five cases;Albright;N. Engl. J. Med.,1937

4. Pseudohypoparathyroidism-an example of “Seabright-Bantam syndrome”. Report of three cases;Albright;Endocrinology,1942

5. Diffuse progressive degeneration of the gray matter of the cerebrum;Alpers;Arch. Neurol. Psychiatry,1931

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