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Results:
1-9
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Results: 9
Authors:
Stephens, Karen
Green, Philip
Ricardi, Vincent M.
Ng, Siu
Rising, Marcia
Barker, David
Darby, John K.
Falls, Kathleen M.
Collins, Francis S.
Willard, Huntington F.
Donis-Keller, Helen
Citation: Stephens, Karen et al., Genetic analysis of eight loci tightly linked to neurofibromatosis I, American journal of human genetics , 44(1), 1989, pp. 13-19
Authors:
Boehnke, Michael
Arnheim, Norman
Li, Honghua
Collins, Francis S.
Citation: Boehnke, Michael et al., Fine structure genetic mapping of human chromosomes using the polymerase chain reaction on single sperm: experimental design considerations, American journal of human genetics , 45-I(1), 1989, pp. 21-32
Authors:
Diehl, Scott R.
Boehnke, Michael
Erickson, Robert P.
Ploughman, Lynn M.
Seiler, Kathleen A.
Lieberman, Janice L.
Clarke, H. Bush
Bruce, Melissa A.
Schorry, Elizabeth K.
Pericak-Vance, Margaret
O'Connell, Peter
Collins, Francis S.
Citation: R. Diehl, Scott et al., A refined genetic map of the region of chromosome 17 surrounding the von recklinghausen neurofibromatosis (NFI) gene, American journal of human genetics , 44(1), 1989, pp. 33-37
Authors:
Fountain, Jane W.
Wallace, Margaret R.
Brereton, Anne M.
O'Connell, Peter
White, Raymond L.
Rich, Donna C.
Ledbetter, David H.
Leach, Robin J.
Fournier, R. E. Keith
Menon, Anil G.
Gusella, James F.
Barker, David
Stephens, Karen
Collins, Francis S.
Citation: W. Fountain, Jane et al., Physical mapping of the von recklinghausen neurofibromatosis region on chromosome 17, American journal of human genetics , 44(1), 1989, pp. 58-67
Authors:
Iannuzzi, Michael C.
Stern, Robert C.
Collins, Francis S.
Tom Hon, Catherine
Hidaka, Noriko
Strong, Theresa
Becker, Lisa
Drumm, Mitchell L.
White, Marga B.
Gerrard, Bernard
Dean, Michael
Citation: C. Iannuzzi, Michael et al., Two frameshift mutations in the cystic fibrosis gene, American journal of human genetics , 48-I(2), 1991, pp. 227-231
Authors:
Merry, Diane E.
Lesko, John G.
Sosnoski, Donna M.
Lewis, Richard A.
Lubinsky, Mark
Trask, Barbara
van den Engh, Ger
Collins, Francis S.
Nussbaum, Robert L.
Citation: E. Merry, Diane et al., Choroideremia and deafness with stapes fixation: a contiguous gene deletion syndrome in Xq21, American journal of human genetics , 45-I(4), 1989, pp. 530-540
Authors:
lannuzzi, Michael C.
Dean, Michael
Drumm, Mitchell L.
Hidaka, Noriko
Cole, Jeffery L.
Perry, Anjanette
Stewart, Claudia
Gerrard, Bernard
Collins, Francis S.
Citation: C. Lannuzzi, Michael et al., Isolation of additional polymorphic clones from the cystic fibrosis region, using chromosome jumping from D7S8, American journal of human genetics , 44(5), 1989, pp. 695-703
Authors:
Iannuzzi, Michael C.
Hidaka, Noriko
Boehnke, Michael
Bruck, Mary E.
Hanna, Wahid T.
Collins, Francis S.
Ginsburg, David
Citation: C. Iannuzzi, Michael et al., Analysis of the relationship of von Willebrand disease (vWD) and hereditary hemorrhagic telangiectasia and identification of a potential type IIA vWD mutation (IIe865 to Thr)., American journal of human genetics , 48-II(4), 1991, pp. 757-763
Authors:
Bloch, Donald B.
Bloch, Kenneth D.
lannuzzi, Michael
Collins, Francis S.
Neer, Eva J.
Seidman, J. G.
Morton, Cynthia C.
Citation: B. Bloch, Donald et al., The gene for the a; subunit of human guanine nucleotide binding protein maps near the cystic fibrosis locus, American journal of human genetics , 42(6), 1988, pp. 884-888
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