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Results: 6

Authors: PAZNEKAS WA CUNNINGHAM ML HOWARD TD KORF BR LIPSON MH GRIX AW FEINGOLD M GOLDBERG R BOROCHOWITZ Z ALECK K MULLIKEN J YIN MF JABS EW
Citation: Wa. Paznekas et al., GENETIC-HETEROGENEITY OF SAETHRE-CHOTZEN-SYNDROME, DUE TO TWIST AND FGFR MUTATIONS, American journal of human genetics, 62(6), 1998, pp. 1370-1380

Authors: KINIRY JR WILLIAMS JR VANDERLIP RL ATWOOD JD REICOSKY DC MULLIKEN J COX WJ MASCAGNI HJ HOLLINGER SE WIEBOLD WJ
Citation: Jr. Kiniry et al., EVALUATION OF 2 MAIZE MODELS FOR 9 US LOCATIONS, Agronomy journal, 89(3), 1997, pp. 421-426

Authors: BLANTON SH CROWDER E MALCOLM S WINTER R GASSER DL STAL S MULLIKEN J HECHT JT
Citation: Sh. Blanton et al., EXCLUSION OF LINKAGE BETWEEN CLEFT-LIP WITH OR WITHOUT CLEFT-PALATE AND MARKERS ON CHROMOSOME-4 AND CHROMOSOME-6, American journal of human genetics, 58(1), 1996, pp. 239-241

Authors: BOON L BURROWS P PALTIEL H EZEKOWITZ A MULLIKEN J
Citation: L. Boon et al., MANAGEMENT OF VASCULAR ANOMALIES OF THE LIVER IN INFANCY - A 25 YEAR EXPERIENCE, Pediatric research, 37(4), 1995, pp. 135-135

Authors: EZEKOWITZ A MULLIKEN J FOLKMAN J
Citation: A. Ezekowitz et al., ADDITIONAL CORRECTIONS - INTERFERON FOR HEMANGIOMAS OF INFANCY, The New England journal of medicine, 333(9), 1995, pp. 595-596

Authors: LI X MA L SNEAD M HAWORTH I SPARKES R JACKSON C WARMAN M MULLIKEN J MAXSON R MULLER U JABS E
Citation: X. Li et al., A MUTATION IN THE HOMEODOMAIN OF THE MSX2 GENE IN A FAMILY AFFECTED WITH CRANIOSYNOSTOSIS, BOSTON TYPE, American journal of human genetics, 53(3), 1993, pp. 213-213
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