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Ray, P.N.
13605  Ergebnisse:
Personensuche X
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1

The carrier transport properties and photodegradation abili..:

Purkayastha, M.D. ; Middya, S. ; Datta, J....
Materials Chemistry and Physics.  226 (2019)  - p. 362-370 , 2019
Link: https://doi.org/10.1016/..
 
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2

WS23.2 Characterization of the CFTR mutation c.3700A>G info..:

Molinski, S.V. ; Gonska, T. ; Huan, L.J....
Journal of Cystic Fibrosis.  13 (2014)  - p. S43 , 2014
Link: https://doi.org/10.1016/..
 
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3

Autosomal recessive hereditary spastic paraplegia—clinical ..:

Yoon, G. ; Baskin, B. ; Tarnopolsky, M....
neurogenetics.  14 (2013)  3-4 - p. 181-188 , 2013
Link: https://doi.org/10.1007/..
 
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4

Caregiver and adult patient perspectives on the importance ..:

Costain, G. ; Chow, E. W. C. ; Ray, P. N..
Journal of Intellectual Disability Research.  56 (2011)  6 - p. 641-651 , 2011
Link: https://doi.org/10.1111/..
 
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5

G.P.2.06 Walker–Warburg syndrome with POMT1 mutations can b..:

Vajsar, J. ; Baskin, B. ; Swoboda, K....
Neuromuscular Disorders.  18 (2008)  9-10 - p. 736-737 , 2008
Link: https://doi.org/10.1016/..
 
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6

Multiple dissimilar new growths of bone:

Ray, P N ; Galstaun, G
British Journal of Surgery.  25 (2005)  100 - p. 910-914 , 2005
Link: https://doi.org/10.1002/..
 
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7

Spontaneous dislocation of the hip in childhood:

Ray, P N
British Journal of Surgery.  21 (2005)  83 - p. 523-526 , 2005
Link: https://doi.org/10.1002/..
 
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8

Primary actinomycosis of the breast:

Ray, P N ; Tribedi, B P
British Journal of Surgery.  26 (2005)  101 - p. 30-34 , 2005
Link: https://doi.org/10.1002/..
 
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9

Chronic epididymo-orchitis or fibrosis of the testicle of f..:

Ray, P N
British Journal of Surgery.  22 (2005)  86 - p. 264-268 , 2005
Link: https://doi.org/10.1002/..
 
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10

Duchenne/Becker muscular dystrophy: correlation of phenotyp..:

Pillers, De-Ann M. ; Fitzgerald, K.M. ; Duncan, N.M....
Human Genetics.  105 (1999)  1-2 - p. 2-9 , 1999
Link: https://doi.org/10.1007/..
 
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11

Congenital cytoplasmic body myopathy with survival motor ne..:

Vajsar, J. ; Balslev, T. ; Ray, P. N...
Neurology.  51 (1998)  3 - p. 873-875 , 1998
Link: https://doi.org/10.1212/..
 
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12

Molecular diagnosis of non-deletion SMA patients using quan..:

Rochette, C.F. ; Surh, L.C. ; Ray, P.N....
neurogenetics.  1 (1997)  2 - p. 141-147 , 1997
Link: https://doi.org/10.1007/..
 
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13

A Muscle-Specific Enhancer Within Intron 1 of the Human Dys..:

Klamut, H. J. ; Bosnoyan-Collins, L. O. ; Worton, R. G..
Nucleic Acids Research.  25 (1997)  8 - p. 1618-1625 , 1997
Link: https://doi.org/10.1093/..
 
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14

A novel mutation in the Norrie disease gene predicted to di..:

Strasberg, P. ; Liede, H. A. ; Stein, T....
Human Molecular Genetics.  4 (1995)  11 - p. 2179-2180 , 1995
Link: https://doi.org/10.1093/..
 
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15

A novel dystrophin isoform is required for normal retinal e..:

D'Souza, V. N. ; Man, N. t. ; Morris, G. E....
Human Molecular Genetics.  4 (1995)  5 - p. 837-842 , 1995
Link: https://doi.org/10.1093/..
 
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