Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation

Search Page

Filters

My Custom Filters

Publication date

Text availability

Article attribute

Article type

Additional filters

Article Language

Species

Sex

Age

Other

Search Results

155 results

Filters applied: . Clear all
Results are displayed in a computed author sort order. The Publication Date timeline is not available.
Page 1
Sternal malformation/vascular dysplasia association.
Hersh JH, Waterfill D, Rutledge J, Harrod MJ, O'Sheal SF, Verdi G, Martinez S, Weisskopf B. Hersh JH, et al. Among authors: harrod mj. Am J Med Genet. 1985 May;21(1):177-86, 201-2. doi: 10.1002/ajmg.1320210127. Am J Med Genet. 1985. PMID: 4003442
Ring 17 chromosome detected by amniocentesis.
Weinberg AG, Bair JL, Harrod MJ. Weinberg AG, et al. Among authors: harrod mj. Humangenetik. 1975 Jul 23;28(3):269-72. doi: 10.1007/BF00278557. Humangenetik. 1975. PMID: 1150287
A "new" lethal multiple congenital anomaly syndrome: joint contractures, cerebellar hypoplasia, renal hypoplasia, urogenital anomalies, tongue cysts, shortness of limbs, eye abnormalities, defects of the heart, gallbladder agenesis, and ear malformations.
Rutledge JC, Friedman JM, Harrod MJ, Currarino G, Wright CG, Pinckney L, Chen H. Rutledge JC, et al. Among authors: harrod mj. Am J Med Genet. 1984 Oct;19(2):255-64. doi: 10.1002/ajmg.1320190208. Am J Med Genet. 1984. PMID: 6507477
155 results