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Results: 1-9 |
Results: 9
DUPLICATION 10Q22.1-Q25.1 DUE TO INTRACHROMOSOMAL INSERTION - A 2ND CASE
Authors: GOSS PW VOULLAIRE L GARDNER RJM
Citation: Pw. Goss et al., DUPLICATION 10Q22.1-Q25.1 DUE TO INTRACHROMOSOMAL INSERTION - A 2ND CASE, Annales de genetique, 41(3), 1998, pp. 161-163
COMPARATIVE CHROMOSOME PAINTING BETWEEN 2 MARSUPIALS - ORIGINS OF AN XX XY1Y2 SEX-CHROMOSOME SYSTEM/
Authors: TODER R ONEILL RJW WIENBERG J OBRIEN PCM VOULLAIRE L MARSHALLGRAVES JA
Citation: R. Toder et al., COMPARATIVE CHROMOSOME PAINTING BETWEEN 2 MARSUPIALS - ORIGINS OF AN XX XY1Y2 SEX-CHROMOSOME SYSTEM/, Mammalian genome, 8(6), 1997, pp. 418-422
MARKER CHROMOSOMES DEFINED BY MOLECULAR CYTOGENETICS
Authors: VOULLAIRE L EARLE E SLATER H
Citation: L. Voullaire et al., MARKER CHROMOSOMES DEFINED BY MOLECULAR CYTOGENETICS, Cytogenetics and cell genetics, 77(1-2), 1997, pp. 55-55
SHARED DNA-SEQUENCES BETWEEN THE X-CHROMOSOME AND Y-CHROMOSOME IN THETAMMAR WALLABY - EVIDENCE FOR INDEPENDENT ADDITIONS TO EUTHERIAN AND MARSUPIAL SEX-CHROMOSOMES
Authors: TODER R WIENBERG J VOULLAIRE L OBRIEN PCM MACCARONE P GRAVES JAM
Citation: R. Toder et al., SHARED DNA-SEQUENCES BETWEEN THE X-CHROMOSOME AND Y-CHROMOSOME IN THETAMMAR WALLABY - EVIDENCE FOR INDEPENDENT ADDITIONS TO EUTHERIAN AND MARSUPIAL SEX-CHROMOSOMES, Chromosoma, 106(2), 1997, pp. 94-98
CYTOGENETIC AND DNA ANALYSIS OF 2 NEUROECTODERMAL TUMORS WITHOUT A SIMPLE T(11-22)
Authors: SLATER HR TIONG T KONSTANTAKOPOULOS S SHAM C PETROVIC V VOULLAIRE L KANNOURAKIS G
Citation: Hr. Slater et al., CYTOGENETIC AND DNA ANALYSIS OF 2 NEUROECTODERMAL TUMORS WITHOUT A SIMPLE T(11-22), Cancer genetics and cytogenetics, 83(1), 1995, pp. 12-17
ASSOCIATION OF A CHROMOSOME DELETION SYNDROME WITH A FRAGILE SITE WITHIN THE PROTOONCOGENE CBL2
Authors: JONES C PENNY L MATTINA T YU S BAKER E VOULLAIRE L LANGDON WY SUTHERLAND GR RICHARDS RI TUNNACLIFFE A
Citation: C. Jones et al., ASSOCIATION OF A CHROMOSOME DELETION SYNDROME WITH A FRAGILE SITE WITHIN THE PROTOONCOGENE CBL2, Nature, 376(6536), 1995, pp. 145-149
THE FRAGILE SITE FRA11B IS LOCATED WITHIN THE PROTOONCOGENE CBL2 AND IS ASSOCIATED WITH A CHROMOSOME DELETION SYNDROME
Authors: JONES C PENNY L MATTINA T YU S BAKER E VOULLAIRE L LANGDON WY SUTHERLAND GR RICHARDS RI TUNNACLIFFE A
Citation: C. Jones et al., THE FRAGILE SITE FRA11B IS LOCATED WITHIN THE PROTOONCOGENE CBL2 AND IS ASSOCIATED WITH A CHROMOSOME DELETION SYNDROME, American journal of human genetics, 57(4), 1995, pp. 85-85
CLINICAL AND MOLECULAR CHARACTERIZATION OF PATIENTS WITH DISTAL 11Q DELETIONS
Authors: PENNY LA DELLAQUILA M JONES MC BERGOFFEN JA CUNNIFF C FRYNS JP GRACE E GRAHAM JM KOUSSEFF B MATTINA T SYME J VOULLAIRE L ZELANTE L ZENGERHAIN J JONES OW EVANS GA
Citation: La. Penny et al., CLINICAL AND MOLECULAR CHARACTERIZATION OF PATIENTS WITH DISTAL 11Q DELETIONS, American journal of human genetics, 56(3), 1995, pp. 676-683
ASYMMETRY AND SKIN PIGMENTARY ANOMALIES IN CHROMOSOME MOSAICISM
Authors: WOODS CG BANKIER A CURRY J SHEFFIELD LJ SLANEY SF SMITH K VOULLAIRE L WELLESLEY D
Citation: Cg. Woods et al., ASYMMETRY AND SKIN PIGMENTARY ANOMALIES IN CHROMOSOME MOSAICISM, Journal of Medical Genetics, 31(9), 1994, pp. 694-701
Risultati: 1-9 |