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Publications by N Teles
828 a Novel De Novo Mutation of Chromosome 7 [46, XX, DEL(7)(P14.2 P15.1)] in a Child With Feeding Problems
Pediatric Research
Child Health
Pediatrics
Perinatology
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A Novel De Novo Dominant Mutation inISCUassociated With Mitochondrial Myopathy
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A De Novo Complex Chromosomal Rearrangement of 46,XX,t(7;15;13)(p15;q21;q31) in a Female With an Adverse Obstetric History
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A Patient With 45,XX,Gminus-46,XX,Gr Mosaicism.
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A Terminal Deletion of the Long Arm of Chromosome 4 [46,XX,del(4)(q33)] in an Infant With Phenotypic Features of Williams Syndrome.
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A Collection of 1814 Human Chromosome 7-Specific STSs.
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