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Results: 1-9 |
Results: 9

Authors: DONLON TA ZIELKE HR EBERLY A KUSLICH C CROWELL D
Citation: Ta. Donlon et al., APOLIPOPROTEIN-E ALLELE FREQUENCIES IN PATIENTS WITH THE SUDDEN-INFANT-DEATH-SYNDROME (SIDS), American journal of human genetics, 61(4), 1997, pp. 2252-2252

Authors: YANCEY MK HARDIN EL PACHECO C KUSLICH CD DONLON TA
Citation: Mk. Yancey et al., NON-MOSAIC TRISOMY-16 IN A 3RD-TRIMESTER FETUS, Obstetrics and gynecology, 87(5), 1996, pp. 856-860

Authors: PHELAN MC MICHAELIS RC TARLETON JC DONLON TA SKINNER SA
Citation: Mc. Phelan et al., DELETION OF 15Q11-]Q13 IN A MOTHER AND SON WITHOUT FEATURES OF PRADER-WILLI OR ANGELMAN SYNDROME, Cytogenetics and cell genetics, 69(1-2), 1995, pp. 116-116

Authors: MICHAELIS RC SKINNER SA LETHCO BA SIMENSEN RJ DONLON TA TARLETON J PHELAN MC
Citation: Rc. Michaelis et al., DELETION INVOLVING D15S113 IN A MOTHER AND SON WITHOUT ANGELMAN-SYNDROME - REFINEMENT OF THE ANGELMAN-SYNDROME CRITICAL DELETION REGION, American journal of medical genetics, 55(1), 1995, pp. 120-126

Authors: NEIDICH JA BANGS CD HSIEH CL DONLON TA DAHL G
Citation: Ja. Neidich et al., CHROMOSOME-ABERRATIONS IN 4 HEPATOBLASTOMAS, American journal of human genetics, 57(4), 1995, pp. 393-393

Authors: KUSLICH CD GREGORIOKING CC DEFREESE DC MOHAPATRA G KOBORI JA DONLON TA
Citation: Cd. Kuslich et al., A PRADER-WILLI-SYNDROME PATIENT WITH A BALANCED DE-NOVO TRANSLOCATION(4-15)(Q27-Q11.2)PAT, American journal of human genetics, 57(4), 1995, pp. 662-662

Authors: GABERT JA LOPEZ M BANGS CD MARTINA N DONLON TA MANNONI P LEE F
Citation: Ja. Gabert et al., CHARACTERIZATION OF SPONTANEOUS FACTOR-INDEPENDENT CELL-LINES DERIVEDFROM THE HUMAN LEUKEMIC-CELL LINE TF-1 - A DOMINANT EVENT, Leukemia, 8(8), 1994, pp. 1359-1368

Authors: MALCOLM S DONLON TA
Citation: S. Malcolm et Ta. Donlon, REPORT OF THE 2ND INTERNATIONAL WORKSHOP ON HUMAN-CHROMOSOME-15 MAPPING 1994, Cytogenetics and cell genetics, 67(1), 1994, pp. 1-14

Authors: KOBORI JA SETODONLON S GREGORY T BANGS D DONLON TA HSIEH CL
Citation: Ja. Kobori et al., A CASE OF MONOSOMY 4P AND TRISOMY 4Q DERIVED FROM A MEIOTIC RECOMBINATION, American journal of human genetics, 53(3), 1993, pp. 1578-1578
Risultati: 1-9 |