Amiloride-sensitive sodium-hydrogen exchange in osmotically shrunken rabbit red blood cellsJENNINGS, M. L; DOUGLAS, S. M; MCANDREW, P. E et al.American journal of physiology. Cell physiology. 1986, Vol 20, Num 1, pp C32-C40, issn 0363-6143Article

Identification of proximal spinal muscular atrophy carriers and patients by analysis of SMN^T and SMN^C gene copy numberMCANDREW, P. E; PARSONS, D. W; SIMARD, L. R et al.American journal of human genetics. 1997, Vol 60, Num 6, pp 1411-1422, issn 0002-9297Article

Differential diagnosis of hereditary hemochromatosis from other liver disorders by genetic analysis: Gene mutation analysis of patients previously diagnosed with hemochromatosis by liver biopsyBARTOLO, C; MCANDREW, P. E; SOSOLIK, R. C et al.Archives of pathology & laboratory medicine (1976). 1998, Vol 122, Num 7, pp 633-637, issn 0363-0153Article

Identification and characterization of RPTPρ, a novel RPTPμ/κ-like receptor protein tyrosine phosphatase whose expression is restricted to the central nervous systemMCANDREW, P. E; FROSTHOLM, A; WHITE, R. A et al.Molecular brain research. 1998, Vol 56, Num 1-2, pp 9-21, issn 0169-328XArticle

Myoblast transfer in the treatment of Duchenne's muscular dystrophyMENDELL, J. R; KISSEL, J. T; NAGARAJA, H et al.The New England journal of medicine. 1995, Vol 333, Num 13, pp 832-838, issn 0028-4793Article

Diagnosis of spinal muscular atrophy in an SMN non-deletion patient using a quantitative PCR screen and mutation analysisPARSONS, D. W; MCANDREW, P. E; ALLINSON, P. S et al.Journal of medical genetics. 1998, Vol 35, Num 8, pp 674-676, issn 0022-2593Article

The incidence of the gene for thermolabile methylene tetrahydrofolate reductase in African AmericansMCANDREW, P. E; BRANDT, J. T; PEARL, D. K et al.Thrombosis research. 1996, Vol 83, Num 2, pp 195-198, issn 0049-3848Article

Intragenic telSMN mutations : Frequency, distribution, evidence of a founder effect, and modification of the spinal muscular atrophy phenotype by cenSMN copy numberPARSONS, D. W; MCANDREW, P. E; IANNACCONE, S. T et al.American journal of human genetics. 1998, Vol 63, Num 6, pp 1712-1723, issn 0002-9297Article

The survival motor neuron protein in spinal muscular atrophyCOOVERT, D. D; LE, T. T; MCANDREW, P. E et al.Human molecular genetics (Print). 1997, Vol 6, Num 8, pp 1205-1214, issn 0964-6906Article

An 11 base pair duplication in exon 6 of the SMN gene produces a type I spinal muscular atrophy (SMA) phenotype : further evidence for SMN as the primary SMA-determining genePARSONS, D. W; MCANDREW, P. E; MONANI, U. R et al.Human molecular genetics (Print). 1996, Vol 5, Num 11, pp 1727-1732, issn 0964-6906Article