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Results:
1-11
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Results: 11
Authors:
DENDUNNEN JT
KRAAYENBRINK T
VANSCHOONEVELD M
VANDEVOSSE E
DEJONG PTVM
TENBRINK JB
SCHUURMAN E
TIJMES N
VANOMMEN GJB
BERGEN AAB
ANDOLFI G
MONTINI E
LI Y
OUDET C
BOLZ H
KAPLAN J
ORTH U
GAL A
HANAUER A
BARDELLI AM
AYUSO C
DIAZ FJ
BITOUN P
VENTRUTO V
BALLABIO A
FRANCO B
HIRIYANNA KT
BINGHAM EL
MCHENRY C
PAWAR H
COATS C
DARGA T
RICHARDS JE
SIEVING PA
HUOPANIEMI L
RANTALA A
ROSENBERG T
DAHL N
WRIGHT A
DELACHAPELLE A
ALITALO T
LENZNER S
BRUNNER B
FEIL S
NIESLER B
SCHULZ U
PINCKERS A
BLANKENNAGEL A
RUETHER K
KELLNER U
RAPPOLD G
ROPERS HH
KALSCHEUER V
BERGER W
TRUMP D
WALPOLE SM
NICOLAOU A
GAYTHOR SA
PIMENIDES D
GEORGE NDL
MOORE UT
YATES JRW
Citation: Jt. Dendunnen et al., FUNCTIONAL IMPLICATIONS OF THE SPECTRUM OF MUTATIONS FOUND IN 234 CASES WITH X-LINKED JUVENILE RETINOSCHISIS (XLRS), Human molecular genetics (Print), 7(7), 1998, pp. 1185-1192
Authors:
HIRIYANNA KT
PAWAR H
BINGHAM EL
RICHARDS JE
SIEVING PA
Citation: Kt. Hiriyanna et al., X-LINKED RETINOSCHISIS - CLONING OF GENOMIC DNA AND ISOLATION OF TRANSCRIBED SEQUENCES FROM ME XP22.1-22.2 REGION, Investigative ophthalmology & visual science, 37(3), 1996, pp. 3027-3027
Authors:
PAWAR H
BINGHAM EL
HIRIYANNA K
SEGAL M
RICHARDS JE
SIEVING PA
Citation: H. Pawar et al., X-LINKED JUVENILE RETINOSCHISIS - LOCALIZATION BETWEEN (DXS1195, DXS418) AND AFM291WF5 ON A SINGLE YAC, Human heredity, 46(6), 1996, pp. 329-335
Authors:
HOU YC
RICHARDS JE
BINGHAM EL
PAWAR H
SCOTT K
SEGAL M
LUNETTA KL
BOEHNKE M
SIEVING PA
Citation: Yc. Hou et al., LINKAGE STUDY OF BESTS VITELLIFORM MACULAR DYSTROPHY (VMD2) IN A LARGE NORTH-AMERICAN FAMILY, Human heredity, 46(4), 1996, pp. 211-220
Authors:
HOU YC
RICHARDS JE
BINGHAM E
PAWAR H
SCOTT K
SEGAL M
LUNETTA KL
BOEHNKE M
SIEVING PA
Citation: Yc. Hou et al., BESTS VITELLIFORM MACULAR DYSTROPHY (VMD2) - LOCALIZATION BETWEEN D11S903 D11S956 AND ROM1 AND LIKELY EXCLUSION OF ROM1 AS CANDIDATE GENE/, Investigative ophthalmology & visual science, 36(4), 1995, pp. 919-919
Authors:
PAWAR H
BINGHAM EL
LUNETTA KL
SEGAL M
RICHARDS JE
BOEHNKE M
SIEVING PA
Citation: H. Pawar et al., REFINED GENETIC-MAPPING OF JUVENILE X-LINKED RETINOSCHISIS, Human heredity, 45(4), 1995, pp. 206-210
Authors:
TOMBRANTINK J
PAWAR H
SWAROOP A
RODRIQUEZ I
CHADER GJ
Citation: J. Tombrantink et al., LOCALIZATION OF THE GENE FOR PIGMENT EPITHELIUM-DERIVED FACTOR (PEDF)TO CHROMOSOME 17P13.1 AND EXPRESSION IN CULTURED HUMAN RETINOBLASTOMACELLS, Genomics, 19(2), 1994, pp. 266-272
Authors:
YAN D
PAWAR H
STATUM SA
ZHENG K
WONG D
GIBSON L
FUJITA R
SIEVING PA
RICHARDS JE
YANGFENG TL
SWAROOP A
Citation: D. Yan et al., ISOLATION AND REGIONAL LOCALIZATION OF X-LINKED GENOMIC CLONES IDENTIFIED WITH SUBTRACTED RETINAL CDNAS, Cytogenetics and cell genetics, 67(4), 1994, pp. 352-352
Authors:
YAN D
PAWAR H
STATUM S
YANGFENG T
SWAROOP A
Citation: D. Yan et al., ISOLATION OF CANDIDATE GENES FOR X-LINKED RETINAL DISEASES, American journal of human genetics, 53(3), 1993, pp. 1255-1255
Authors:
TOMBRANTINK J
PAWAR H
ANDERSON L
SWAROOP A
STEELE F
RODRIGUEZ I
CHADER GJ
Citation: J. Tombrantink et al., MOLECULAR-CLONING AND CHROMOSOMAL LOCALIZATION OF THE GENE FOR HUMAN PIGMENT EPITHELIUM-DERIVED FACTOR (PEDF), Investigative ophthalmology & visual science, 33(4), 1992, pp. 828-828
Authors:
SWAROOP A
JACKSON A
PAWAR H
XU JZ
SKOLNICK C
AGARWAL N
YANGFENG T
Citation: A. Swaroop et al., REGULATION AND FUNCTION OF A NOVEL CONSERVED NEURAL RETINA-SPECIFIC GENE ENCODING A LEUCINE ZIPPER DOMAIN, Investigative ophthalmology & visual science, 33(4), 1992, pp. 1400-1400
Risultati:
1-11
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