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Extrapolation of adult data and other data in pediatric drug-development programs

Pediatrics (Evanston), 2011-11, Vol.128 (5), p.e1242

2011

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Differential Expansion of the N-Formylpeptide Receptor Gene Cluster in Human and Mouse

Genomics (San Diego, Calif.), 1998-07, Vol.51 (2), p.270-276

1998

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Molecular Cloning, Characterization, and Genetic Mapping of the cDNA Coding for a Novel Secretory Protein of Mouse. DEMONSTRATION OF ALTERNATIVE SPLICING IN SKIN AND CARTILAGE

The Journal of biological chemistry, 1995-07, Vol.270 (27), p.16385-16394

1995

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Genetic mapping of the mouse ferritin light chain gene and 11 pseudogenes on 11 mouse chromosomes

Mammalian genome, 1998-02, Vol.9 (2), p.111-113

1998

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Rat phenol-preferring sulfotransferase genes ( Stp and stp2): localization to mouse chromosomes 7 and 17

Genomics (San Diego, Calif.), 1995-03, Vol.26 (2), p.417-419

1995

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A de novo G+1 → a mutation at the α2(I) exon 16 splice donor site causes skipping of exon 16 in the cDNA of one allele of an OI Type IV proband

Human mutation, 1993, Vol.2 (5), p.380-388

1993

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Intractable vasculitis, resorptive osteolysis, and immunity to type i collagen in type viii ehlers‐danlos syndrome

Arthritis and rheumatism, 1991-11, Vol.34 (11), p.1466-1475

1991

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A Patient with Ehlers-Danlos Syndrome Type VI Is Homozygous for a Premature Termination Codon in Exon 14 of the Lysyl Hydroxylase 1 Gene

Molecular genetics and metabolism, 1999-05, Vol.67 (1), p.74-82

1999

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Molecular Sequence Data
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Adult
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Extrapolation of adult data and other data in pediatric drug-development programs

Differential Expansion of the N-Formylpeptide Receptor Gene Cluster in Human and Mouse

Molecular Cloning, Characterization, and Genetic Mapping of the cDNA Coding for a Novel Secretory Protein of Mouse. DEMONSTRATION OF ALTERNATIVE SPLICING IN SKIN AND CARTILAGE

Genetic mapping of the mouse ferritin light chain gene and 11 pseudogenes on 11 mouse chromosomes

Rat phenol-preferring sulfotransferase genes ( Stp and stp2): localization to mouse chromosomes 7 and 17

A de novo G+1 → a mutation at the α2(I) exon 16 splice donor site causes skipping of exon 16 in the cDNA of one allele of an OI Type IV proband

Intractable vasculitis, resorptive osteolysis, and immunity to type i collagen in type viii ehlers‐danlos syndrome

A Patient with Ehlers-Danlos Syndrome Type VI Is Homozygous for a Premature Termination Codon in Exon 14 of the Lysyl Hydroxylase 1 Gene

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