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The Norrie disease gene maps to a 150 kb region on chromosome Xp11.3
by
Sims, K.B.
,
Lebo, R.V.
,
Benson, G.
,
Shalish, C.
,
Schuback, D.
,
Chen, Z.Y.
,
Bruns, G.
,
Craig, I.W.
,
Golbus, M.S.
,
Breakefield, X.O.
Published in
Human molecular genetics
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Multicolor in situ hybridization and linkage analysis order Charcot-Marie-Tooth type I (CMTIA) gene-region markers
by
LEBO, R. V
,
LYNCH, E. D
,
BIRD, T. D
,
GOLBUS, M. S
,
BARKER, D. F
,
O'CONNELL, P
,
CHANCE, P. F
Published in
American journal of human genetics
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Prenatal treatment of biotin-responsive multiple carboxylase deficiency
by
Packman, S
,
Golbus, M.S
,
Cowan, M.J
,
Sweetman, L
,
Nyhan, W
,
Burri, B.J
,
Baker, H
Published in
Annals of the New York Academy of Sciences
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American Journal Of Human Genetics
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Annals Of The New York Academy Of Sciences
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Human Molecular Genetics
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Chromosome Mapping
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Genes
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Humans
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Pedigree
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Recombination, Genetic
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Base Sequence
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Basic Biological Sciences
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Biological And Medical Sciences
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Biological Markers
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Biotin Deficiency
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Blindness - Congenital
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Blindness - Genetics
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Carboxylase
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Charcot-Marie-Tooth Disease - Genetics
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Child, Preschool
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Chromosome Banding
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Chromosome Deletion
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Chromosomes
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Chromosomes, Fungal
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Ezb Electronic Journals Library
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