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Results: 1-11 |
Results: 11
GENOME SEARCH FOR NON-SYNDROMIC CLEFT-LIP AND PALATE
Authors: ZIMMER J BEIRAGHI S HOOVER D KENYON J KIMBERLING W
Citation: J. Zimmer et al., GENOME SEARCH FOR NON-SYNDROMIC CLEFT-LIP AND PALATE, Journal of dental research, 77, 1998, pp. 630-630
LINKAGE OF A GENE CAUSING HIGH BONE MASS TO HUMAN-CHROMOSOME-11 (11Q12-13)
Authors: JOHNSON ML GONG GD KIMBERLING W RECKER SM KIMMEL DB RECKER RR
Citation: Ml. Johnson et al., LINKAGE OF A GENE CAUSING HIGH BONE MASS TO HUMAN-CHROMOSOME-11 (11Q12-13), American journal of human genetics, 60(6), 1997, pp. 1326-1332
RELATIONSHIP OF MUTATIONS IN THE ADPKD1 GENE WITH CLINICAL MANIFESTATIONS IN AUTOSOMAL-DOMINANT POLYCYSTIC KIDNEY-DISEASE PATIENTS
Authors: GABOW P JOHNSON A KIMBERLING W OVERBECK L
Citation: P. Gabow et al., RELATIONSHIP OF MUTATIONS IN THE ADPKD1 GENE WITH CLINICAL MANIFESTATIONS IN AUTOSOMAL-DOMINANT POLYCYSTIC KIDNEY-DISEASE PATIENTS, Journal of the American Society of Nephrology, 7(9), 1996, pp. 1820-1820
CONSTRUCTION OF NOTI LINKING LIBRARIES AND YAC CONTIGS TO MAP THE CRITICAL REGION OF USH2A IN 1Q41
Authors: EUDY J TALMADGE C BERGLUND P ZHEN DK WANG JY WESTON M KIMBERLING W SUMEGI J
Citation: J. Eudy et al., CONSTRUCTION OF NOTI LINKING LIBRARIES AND YAC CONTIGS TO MAP THE CRITICAL REGION OF USH2A IN 1Q41, Cytogenetics and cell genetics, 72(2-3), 1996, pp. 148-148
CLEFT-LIP PALATE, NO EVIDENCE FOR LINKAGE TO 6P
Authors: BEIRAGHI S CONNLY C HOOVER D KIMBERLING W
Citation: S. Beiraghi et al., CLEFT-LIP PALATE, NO EVIDENCE FOR LINKAGE TO 6P, Journal of dental research, 75, 1996, pp. 1735-1735
DETECTION OF FREQUENT MUTATIONS IN THE PKD1 GENE
Authors: DAMODARASAMY M DOBIN A GABOW P JOHNSON A KIMBERLING W
Citation: M. Damodarasamy et al., DETECTION OF FREQUENT MUTATIONS IN THE PKD1 GENE, Journal of the American Society of Nephrology, 6(3), 1995, pp. 719-719
CLINICAL FINDINGS IN OBLIGATE CARRIERS OF TYPE-I USHER SYNDROME
Authors: WAGENAAR M TERRAHE B VANAAREM A HUYGEN P ADMIRAAL R BLEEKERWAGEMAKERS E PINCKERS A KIMBERLING W CREMERS C
Citation: M. Wagenaar et al., CLINICAL FINDINGS IN OBLIGATE CARRIERS OF TYPE-I USHER SYNDROME, American journal of medical genetics, 59(3), 1995, pp. 375-379
CONFIRMATION OF LOCALIZATION OF VANDERWOUDE GENE TO 1Q32-41 REGION
Authors: BEIRAGHI S GERBER J HOOVER D DOBIN A FOWLER T TINLEY S BRENNAN K KIMBERLING W
Citation: S. Beiraghi et al., CONFIRMATION OF LOCALIZATION OF VANDERWOUDE GENE TO 1Q32-41 REGION, American journal of human genetics, 57(4), 1995, pp. 1867-1867
UTILITY OF ULTRASONOGRAPHY (US) IN CHILDREN (C) IN FAMILIES WITH CHROMOSOME-16 AUTOSOMAL-DOMINANT POLYCYSTIC KIDNEY-DISEASE (ADPKD1)
Authors: GABOW P JOHNSON A KIMBERLING W VELIDI M FOWLER T STRAIN J
Citation: P. Gabow et al., UTILITY OF ULTRASONOGRAPHY (US) IN CHILDREN (C) IN FAMILIES WITH CHROMOSOME-16 AUTOSOMAL-DOMINANT POLYCYSTIC KIDNEY-DISEASE (ADPKD1), Journal of the American Society of Nephrology, 5(3), 1994, pp. 646-646
AUTOSOMAL-DOMINANT POLYCYSTIC KIDNEY-DISEASE IN BLACKS - CLINICAL COURSE AND EFFECTS OF SICKLE-CELL HEMOGLOBIN
Authors: YIUM J GABOW P JOHNSON A KIMBERLING W MARTINEZMALDONADO M
Citation: J. Yium et al., AUTOSOMAL-DOMINANT POLYCYSTIC KIDNEY-DISEASE IN BLACKS - CLINICAL COURSE AND EFFECTS OF SICKLE-CELL HEMOGLOBIN, Journal of the American Society of Nephrology, 4(9), 1994, pp. 1670-1674
EXCLUSION MAP FOR THE 2ND LOCUS OF AUTOSOMAL-DOMINANT POLYCYSTIC KIDNEY-DISEASE (ADPKD2)
Authors: SOMLO S REYNOLDS D TORRES V THIBODEAU S ROMEO G CECCHERINI I MORGAN J PARFREY P GABOW P KIMBERLING W
Citation: S. Somlo et al., EXCLUSION MAP FOR THE 2ND LOCUS OF AUTOSOMAL-DOMINANT POLYCYSTIC KIDNEY-DISEASE (ADPKD2), American journal of human genetics, 53(3), 1993, pp. 1081-1081
Risultati: 1-11 |