Fragile sites on human chromosomes

Bằng Howard-Peebles, Patricia N.
Được phát hành 1986

A complex chromosome rearrangement resulting in trisomy 15q22→qter

Bằng Howard-Peebles, Patricia N, Scarbrough, Paula R, Sharpe, Joe, Finley, Wayne H, Finley, Sara C
Được phát hành 1982

The Registry of Cytogenetic Abnormalities and Phenylketonuria (ReCAP): System Description and Data Integrity

Bằng Mize, Susan G., Friedman, J. M., Howard-Peebles, Patricia N., Lerner, Barbara, Mize, Charles E., Smith, Janet P.
Được phát hành 1985

Survey of the Fragile X Syndrome CGG Repeat and the Short-Tandem-Repeat and Single-Nucleotide-Polymorphism Haplotypes in an African American Population

Bằng Crawford, Dana C., Schwartz, Charles E., Meadows, Kellen L., Newman, James L., Taft, Lisa F., Gunter, Chris, Brown, W. Ted, Carpenter, Nancy J., Howard-Peebles, Patricia N., Monaghan, Kristin G., Nolin, Sarah L., Reiss, Allan L., Feldman, Gerald L., Rohlfs, Elizabeth M., Warren, Stephen T., Sherman, Stephanie L.
Được phát hành 2000

Fragile X Premutation Is a Significant Risk Factor for Premature Ovarian Failure: The International Collaborative POF in Fragile X Study—Preliminary Data

Bằng Allingham-Hawkins, Diane J., Babul-Hirji, Riyana, Chitayat, David, Holden, Jeanette J.A., Yang, Kathy T., Lee, C., Hudson, R., Gorwill, H., Nolin, Sarah L., Glicksman, Anne, Jenkins, Edmund C., Brown, W. Ted, Howard-Peebles, Patricia N., Becchi, Cindy, Cummings, Emilie, Fallon, Lee, Seitz, Suzanne, Black, Susan H., Vianna-Morgante, Angela M., Costa, Silvia S., Otto, Paulo A., Mingroni-Netto, Regina C., Murray, Anna, Webb, J., MacSwinney, F., Dennis, N., Jacobs, Patricia A., Syrrou, Maria, Georgiou, Ioannis, Patsalis, Phillipos C., Uzielli, Maria L. Giovannucci, Guarducci, S., Lapi, E., Cecconi, A., Ricci, U., Ricotti, G., Biondi, C., Scarselli, B., Vieri, F.
Được phát hành 1999