Fragile sites on human chromosomes

Yazar: Howard-Peebles, Patricia N.
Baskı/Yayın Bilgisi 1986

A complex chromosome rearrangement resulting in trisomy 15q22→qter

Yazar: Howard-Peebles, Patricia N, Scarbrough, Paula R, Sharpe, Joe, Finley, Wayne H, Finley, Sara C
Baskı/Yayın Bilgisi 1982

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

Yazar: Mize, Susan G., Friedman, J. M., Howard-Peebles, Patricia N., Lerner, Barbara, Mize, Charles E., Smith, Janet P.
Baskı/Yayın Bilgisi 1985

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

Yazar: 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.
Baskı/Yayın Bilgisi 2000

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

Yazar: 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.
Baskı/Yayın Bilgisi 1999