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51. Chimpanzee and Human Y Chromosomes Are Remarkably Divergent in Structure and Gene Content

52. Tissue-specific variation in DNA methylation levels along human chromosome 1

53. Flow Cytometry and Sorting, 2d ed

55. Comparative Analyses of Chromosome Alterations in Soft-Tissue Metastases within and across Patients with Castration-Resistant Prostate Cancer

56. Genomic Alterations Indicate Tumor Origin and Varied Metastatic Potential of Disseminated Cells from Prostate Cancer Patients

57. A sequence-based survey of the complex structural organization of tumor genomes

61. 220: Array Comparative Genomic Hybridization Analysis of Disseminated Epithelial Cells from the Blood and Bone Marrow of Men with Clinically Localized Prostate Cancer

63. Array Comparative Genomic Hybridization Analysis of Genomic Alterations in Breast Cancer Subtypes

65. Identification of a Novel Gene on Chromosome 7q11.2 Interrupted by a Translocation Breakpoint in a Pair of Autistic Twins

79. Alagille syndrome is caused by mutations in human Jagged1, which encodes a ligand for Notch1

83. Smith‐Magenis syndrome deletion: A case with equivocal cytogenetic findings resolved by fluorescence in situ hybridization

89. Integration of physical, genetic and cytogenetic maps of human chromosome 7: isolation and analysis of yeast artificial chromosome clones for 117 mapped genetic markers

91. Physical mapping of the holoprosencephaly critical region on chromosome 7q36

92. Somatic cell hybrids, sequence-tagged sites, simple repeat polymorphisms, and yeast artificial chromosomes for physical and genetic mapping of proximal 17p

94. The gene for the peripheral myelin protein PMP–22 is a candidate for Charcot–Marie–Tooth disease type 1A

95. Evolution of the mammalian G protein α subunit multigene family

98. DNA duplication associated with Charcot-Marie-Tooth disease type 1A

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