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The American Journal of Human Genetics, ISSN 0002-9297, 1999, Volume 64, Issue 4, pp. 1024 - 1035
Journal Article
Nature genetics, ISSN 1061-4036, 1999, Volume 23, Issue 2, pp. 217 - 221
Retinitis pigmentosa (RP) comprises a clinically and genetically heterogeneous group of diseases that afflicts approximately 1.5 million people worldwide.... 
PROTEIN | GENE | EPITHELIAL-CELL LINE | LAMININ | SEQUENCE | GENETICS & HEREDITY | RECEPTOR | EPIDERMAL GROWTH-FACTOR | PROTEOGLYCAN | DOMAINS | EXPRESSION | CRB1 protein | amino acid sequence prediction | Retina | nucleotide sequence | RET3C11 gene | Laminin | chromosome 1 | retinitis pigmentosa | Lectins | Photoreceptors | cDNA | man | epidermal growth factor | crumbs protein | Humans | Molecular Sequence Data | Family Health | Male | Polymorphism, Single-Stranded Conformational | Tissue Distribution | crumbs protein, Drosophila | Chromosomes, Human, Pair 1 | Retinitis Pigmentosa | DNA Mutational Analysis | Gene Expression Regulation, Developmental | Base Sequence | Female | Amino Acid Sequence | Cell Line | Drosophila Proteins | Chromosome Mapping | Sequence Analysis, DNA | Index Medicus | Membrane Proteins | Homozygote | Point Mutation | Blotting, Northern | Animals | Pedigree | Mutagenesis, Insertional | Mutation | Alu Elements | Drosophila melanogaster | Eye Proteins | RNA, Messenger | Amino Acid Substitution | DNA, Complementary | DNA, Complementary - genetics | RNA, Messenger - metabolism | Drosophila melanogaster - genetics | Eye Proteins - genetics | Chromosomes, Human, Pair 1 - genetics | Alu Elements - genetics | Membrane Proteins - genetics | RNA, Messenger - genetics | Retinitis Pigmentosa - genetics | DNA, Complementary - chemistry | Retinitis Pigmentosa - pathology
Journal Article
Journal Article
Journal Article
Genomics, ISSN 0888-7543, 1989, Volume 4, Issue 1, pp. 41 - 46
Characterization of several male-viable deletions and duplications with 20 random DNA probes has enabled us to subdivide the Xq21 region into seven discernible... 
GENETICS & HEREDITY | mapping | deletion | choroideremia | use | X chromosome | association | syndromes | loci | man | Chromosome Deletion | DNA Probes | Multigene Family | Deafness - genetics | Retinal Degeneration - genetics | Humans | X Chromosome | Male | Restriction Mapping | Syndrome | Genetic Linkage | Intellectual Disability - genetics | Index Medicus
Journal Article
Journal Article
Journal Article
2000, CEDLA Latin America studies, ISBN 9789070280871, Volume 87, x, 380
Book
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