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Results: 5

Authors: FELDMAN GJ WARD DE ROBIN NH ARONSON AL ZACKAI UH SAAVEDRA D PROUD V ROBB LJ KALOUSTIAN V JABS E CAREY JC MUNNICH A COHEN MM PRICE RA MUENKE M
Citation: Gj. Feldman et al., NOVEL X-LINKED INHERITANCE PATTERN IN CRANIOFRONTONASAL SYNDROME, Journal of dental research, 76, 1997, pp. 3073-3073

Authors: MASHKOVA TD TYUMENEVA IG ZINOVEVA OL ROMANOVA LY JABS E ALEKSANDROV IA
Citation: Td. Mashkova et al., CENTROMERIC ALPHA-SATELLITE DNA AT EUCHROMATIN HETEROCHROMATIN BOUNDARY OF HUMAN-CHROMOSOME-21/, Molecular biology, 30(5), 1996, pp. 617-625

Authors: JABS E
Citation: E. Jabs, JACKSON-WEISS AND CROUZON SYNDROMES ARE ALLELIC WITH MUTATIONS IN FIBROBLAST GROWTH-FACTOR RECEPTOR 2 (VOL 8, PG 275, 1995), Nature genetics, 9(4), 1995, pp. 451-451

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

Authors: LEWANDA A COHEN M JACKSON C TAYLOR E BELOFF M DAY D CLARREN S ORTIZ RI GARCIA C HAUSELMAN E FIGUEROA A WULFSBERG E WARMAN M REID C ZACKAI E JABS E
Citation: A. Lewanda et al., GENETIC-HETEROGENEITY AMONG CRANIOSYNOSTOSIS SYNDROMES - REFINING THESAETHRE-CHOTZEN SYNDROME LOCUS POSITION TO AND EXCLUSION OF JACKSON-WEISS AND CROUZON SYNDROME LOCI FROM DISTAL-7P, American journal of human genetics, 53(3), 1993, pp. 245-245
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