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Results: 1-8 |
Results: 8
GENE SYMBOL - COL11A1 - DISEASE - MARSHALL-SYNDROME
Authors: MEISLER MH GRIFFITH AJ WARMAN M TILLER G SPRUNGER LK
Citation: Mh. Meisler et al., GENE SYMBOL - COL11A1 - DISEASE - MARSHALL-SYNDROME, Human genetics, 102(4), 1998, pp. 498-498
THERAPY FOR YOUTHS WITH ANXIETY DISORDERS - A SECOND RANDOMIZED CLINICAL-TRIAL
Authors: KENDALL PC FLANNERYSCHROEDER E PANICHELLIMINDEL SM SOUTHAMGEROW M HENIN A WARMAN M
Citation: Pc. Kendall et al., THERAPY FOR YOUTHS WITH ANXIETY DISORDERS - A SECOND RANDOMIZED CLINICAL-TRIAL, Journal of consulting and clinical psychology, 65(3), 1997, pp. 366-380
DYSFUNCTIONAL AND ANTIGENICALLY ABNORMAL C1Q RESULTING FROM A POINT MUTATION IN CODON-6 OF THE C-CHAIN
Authors: SUWAIRI W BAHABRI S BEVING D WISNIESKI J WARMAN M
Citation: W. Suwairi et al., DYSFUNCTIONAL AND ANTIGENICALLY ABNORMAL C1Q RESULTING FROM A POINT MUTATION IN CODON-6 OF THE C-CHAIN, Arthritis and rheumatism, 40(9), 1997, pp. 1662-1662
GENETIC-HETEROGENEITY IN STICKLER-SYNDROME - PHENOTYPIC EXPLORATION
Authors: WILKIN DJ LIBERFARB R MORTIER GR WARMAN M COHN DH FRANCOMANO CA
Citation: Dj. Wilkin et al., GENETIC-HETEROGENEITY IN STICKLER-SYNDROME - PHENOTYPIC EXPLORATION, American journal of human genetics, 61(4), 1997, pp. 2055-2055
ASSEMBLY AND SEQUENCING OF A CDNA COVERING THE ENTIRE MOUSE ALPHA-1(IX) COLLAGEN CHAIN
Authors: ROKOS I MURAGAKI Y WARMAN M OLSEN BR
Citation: I. Rokos et al., ASSEMBLY AND SEQUENCING OF A CDNA COVERING THE ENTIRE MOUSE ALPHA-1(IX) COLLAGEN CHAIN, Matrix biology, 14(1), 1994, pp. 1-8
LINKAGE OF TYPICAL PSEUDOACHONDROPLASIA TO CHROMOSOME-19
Authors: HECHT JT FRANCOMANO CA BRIGGS MD DEERE M CONNER B HORTON WA WARMAN M COHN DH BLANTON SH
Citation: Jt. Hecht et al., LINKAGE OF TYPICAL PSEUDOACHONDROPLASIA TO CHROMOSOME-19, Genomics, 18(3), 1993, pp. 661-666
A MUTATION IN THE HOMEODOMAIN OF THE MSX2 GENE IN A FAMILY AFFECTED WITH CRANIOSYNOSTOSIS, BOSTON TYPE
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
GENETIC-HETEROGENEITY AMONG CRANIOSYNOSTOSIS SYNDROMES - REFINING THESAETHRE-CHOTZEN SYNDROME LOCUS POSITION TO AND EXCLUSION OF JACKSON-WEISS AND CROUZON SYNDROME LOCI FROM DISTAL-7P
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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