Fourier transform SERS studies of the chemisorption of ferricyanide on gold electrode surfacesLOWRY, R. B.Spectrochimica acta. Part A : Molecular spectroscopy. 1993, Vol 49, Num 5-6, pp 831-836, issn 0584-8539Article

SERS and Fourier transform SERS studies of the hexacyanoferrate (III)-hexacyanoferrate(II) couple on gold electrode surfacesLOWRY, R. B.Journal of Raman spectroscopy. 1991, Vol 22, Num 12, pp 805-809, issn 0377-0486Article

Overlap between Rubinstein-Taybi and Saethre-Chotzen syndromes : a case reportLOWRY, R. B.American journal of medical genetics. Supplement. 1990, Num 6, pp 73-76, issn 1040-3787, 4 p.Article

Father-to-Son Transmission of an X-linked Gene: Case of Paternal Sex Chromosome HeterodisomyFERRIER, R. A; LOWRY, R. B; LEMIRE, E. G et al.American journal of medical genetics. Part A. 2009, Vol 149, Num 12, pp 2871-2873, issn 1552-4825, 3 p.Article

Analysis of sperm chromosome complements from a man heterozygous for a pericentric inversion of chromosome 1MARTIN, R. H; CHERNOS, J. E; LOWRY, R. B et al.Human genetics. 1994, Vol 93, Num 2, pp 135-138, issn 0340-6717Article

Interstidial deletion for a region in the long arm of chromosome 16LIN, C. C; LOWRY, R. B; SNYDER, F. F et al.Human genetics. 1983, Vol 65, Num 2, pp 134-138, issn 0340-6717Article

Bowen-Conradi syndrome: A clinical and genetic studyLOWRY, R. B; INNES, A. M; MORGAN, K et al.American journal of medical genetics. 2003, Vol 120A, Num 3, pp 423-428, issn 0148-7299, 6 p.Article

An interstitial deletion of the long arm of chromosome 13ROLAND, B; LOWRY, R. B; ROBERTSON, A. S et al.Clinical genetics. 1989, Vol 35, Num 4, pp 276-281, issn 0009-9163, 6 p.Article

Keutel syndrome: clinical report and literature reviewCORMODE, E. J; DAWSON, M; LOWRY, R. B et al.American journal of medical genetics. 1986, Vol 24, Num 2, pp 289-294, issn 0148-7299Article

Syndrome of multiple epiphyseal dysplasia (ribbing type) with rhizomelic shortness, cleft palate, and micrognathia in two unrelated patientsLOWRY, R. B; WESENBERG, R. L; HALL, J. G et al.American journal of medical genetics. 1996, Vol 63, Num 1, pp 55-61, issn 0148-7299Article

Autosomal recessive, fatal infantile hypertonic muscular dystrophy among Canadian nativesLACSON, A. G; SESHIA, S. S; LOWRY, N. J et al.Canadian journal of neurological sciences. 1994, Vol 21, Num 3, pp 203-212, issn 0317-1671Conference Paper

Familial complex chromosomal rearrangement resulting in duplication/deletion of 6q14 to 6q16ROLAND, B; LOWRY, R. B; COX, D. M et al.Clinical genetics. 1993, Vol 43, Num 3, pp 117-121, issn 0009-9163Article

Lincoln vs. Douglas again; comments on the papers by Curry et al, Greenberg et al, and Belmont et alOPITZ, J. M; LOWRY, R. B.American journal of medical genetics. 1987, Vol 26, Num 1, pp 69-71, issn 0148-7299Article

Lincoln vs. Douglas again; comments on the papers by Curry et al, Greenberg et al, and Belmont et alOPITZ, J. M; LOWRY, R. B.American journal of medical genetics. 1987, Vol 26, Num 1, pp 69-71, issn 0148-7299Article

Mental retardation, distinct facial changes, short stature, obesity, and hypogonadism: a new X-linked mental retardation syndromeCHUDLEY, A. E; LOWRY, R. B; HOAR, D. I et al.American journal of medical genetics. 1988, Vol 31, Num 4, pp 741-751, issn 0148-7299Article

Congenital anomalies in American Indians of British ColumbiaLOWRY, R. B; THUNEM, N. Y; SILVER, M et al.Genetic epidemiology. 1986, Vol 3, Num 6, pp 455-467, issn 0741-0395Article

Recurrent de novo interstitial deletion of 16q in two mentally retarded sistersHOO, J. J; LOWRY, R. B; LIN, C. C et al.Clinical genetics. 1985, Vol 27, Num 4, pp 420-425, issn 0009-9163Article

CAMPS: computer-automated metacarpophalangeal profile systemCOUPLAND, S. G; MCLEOD, D. R; WESENBERG, R. L et al.American journal of medical genetics. 1985, Vol 22, Num 2, pp 375-381, issn 0148-7299Article

Juvenile cataract in HutteritesSHOKEIR, M. H. K; LOWRY, R. B.American journal of medical genetics. 1985, Vol 22, Num 3, pp 495-500, issn 0148-7299Article

Cleft lip and palate, sensorineural deafness, and sacral lipoma in two brothers : a possible example of the disorganisation mutantLOWRY, R. B; SIU-LI YONG.Journal of medical genetics. 1991, Vol 28, Num 2, pp 135-137, issn 0022-2593Article

Co-Occurrence of Joubert Syndrome and Jeune Asphyxiating Thoracic DystrophyLEHMAN, A. M; EYDOUX, P; TRNKA, P et al.American journal of medical genetics. Part A. 2010, Vol 152, Num 6, pp 1411-1419, issn 1552-4825, 9 p.Article

Association between congenital foot anomalies and gestational age at amniocentesisYOON, G; CHERNOS, J; SIBBALD, B et al.Prenatal diagnosis. 2001, Vol 21, Num 13, pp 1137-1141, issn 0197-3851Article

Epiphyseal dysplasia, microcephaly, nystagmus, and retinitis pigmentosaLOWRY, R. B; WOOD, B. J; COX, T. A et al.American journal of medical genetics. 1989, Vol 33, Num 3, pp 341-345, issn 0148-7299Article

An electrochemical and SERS investigation of the influence of pH on the effectiveness of some corrosion inhibitors of copperMUSIANI, M. M; MENGOLI, G; FLEISCHMANN, M et al.Journal of electroanalytical chemistry and interfacial electrochemistry. 1987, Vol 217, Num 1, pp 187-202, issn 0022-0728Article

The Grant syndrome: persistent Wormian bones, blue sclerae, mandibular hypoplasia, shallow glenoid fossae and campomelia ― an autosomal dominant traitMACLEAN, J. R; LOWRY, R. B; WOOD, B. J et al.Clinical genetics. 1986, Vol 29, Num 6, pp 523-529, issn 0009-9163Article