HUM-MOLGEN DIAGnostics/Clinical Research

17 June 1997

GREIG CEPHALOPOLYSYNDACTYLY SYNDROME

The National Human Genome Research Institute is soliciting patients with Greig Cephalopolysyndactyly syndrome for a research study. The purpose of the study is to perform clinical and molecular characterization of sporadic and familial cases of this disorder. Subjects accepted into the study will receive paid travel to the NIH, a medical genetics evaluation, appropriate imaging studies, and specimen acquisition for development of clinical diagnostics and genotype-phenotype correlation.

PLEASE NOTE AS OF JANUARY, 1997:

We are now OFFICIALLY the National Human Genome Research Institute (NHGRI). PLEASE NOTE NEW EMAIL ADDRESS. Ann CM Smith, M.A., CGC Translational Research & Laboratory Support Unit Protocol and Laboratory Support Core Medical Genetics Branch, NHGRI-NIH BLDG 10, Room 3D53 10 Center Drive, MSC 1267 Bethesda, MD 20892-1267

NIH office: 301-402-2011 NIH FAX 301-435-3495 (NEW FAX) NIH email acmsmith@nhgri.nih.gov BEEPER 202-539-4091 (at the tone enter your telephone number with AC and then the # sign Home/PRISMS/FAX 703-709-0568

For information on eligibility and details about the study please contact:

Principal Investigator:

Leslie Biesecker, M.D., 301-402-2041 or leslieb@helix.nih.gov
Mailing address: 49 Convent Dr., Bldg 49 Room 4A80, Bethesda, MD 20892

Study Coordinator:

Kathy Peters, M.S.
Medical Genetics Branch, NHGRI
10 Center Drive, Bldg 10, Room 10C101, Bethesda, MD 20892, 301-402-9653 Email: kpeters@nhgri.nih.gov