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Results: 1-5 |
Results: 5

Authors: RUGARLI E DALZOTTO L QUADERI N ELLIOTT R LINGERFELTER PA CARREL L THOMAS S WILLARD H DISTECHE C BALLABIO A
Citation: E. Rugarli et al., CHARACTERIZATION OF THE MURINE MID1 GENE - IMPLICATIONS FOR THE PATHOGENESIS OF OPITZ-SYNDROME AND THE EVOLUTION OF THE MAMMALIAN PSEUDOAUTOSOMAL REGION, European journal of human genetics, 6, 1998, pp. 805-805

Authors: WILLARD H SALZ HK
Citation: H. Willard et Hk. Salz, DOSAGE COMPENSATION - REMODELING CHROMATIN WITH RNA, Nature, 386(6622), 1997, pp. 228-229

Authors: TRANEBJAERG L LUBS HA BORGHGRAEF M BROWN WT FISCH G FRYNS JP HAGERMAN R JACOBS PA MANDEL JL MULLEY J OOSTRA B SCHWARTZ C SHERMAN S WILLARD H WILLEMS P
Citation: L. Tranebjaerg et al., 7TH INTERNATIONAL WORKSHOP ON THE FRAGILE-X-LINKED AND X-LINKED MENTAL-RETARDATION, American journal of medical genetics, 64(1), 1996, pp. 1-14

Authors: ALITALO T FRANCIS F JOHNSON D KERE J LEHRACH H DELACHAPELLE A WILLARD H
Citation: T. Alitalo et al., A-SIMILAR-OR-EQUAL-TO-5 MB YAC CONTIG IN XP22.1-]P22.2 SPANNING THE DXS69, XE59, GLRA2, PIGA, GRPR AND CABP LOCI, Cytogenetics and cell genetics, 67(4), 1994, pp. 329-329

Authors: XING Y CLEMSON C COLEMAN J BROWN C WILLARD H LAWRENCE J
Citation: Y. Xing et al., EVIDENCE SUGGESTING THE STABLE ASSOCIATION OF XIST RNA WITH THE INACTIVE X-CHROMOSOME, American journal of human genetics, 53(3), 1993, pp. 227-227
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