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Results of search for 'au:"STEVENSON, R E"', page 4 of 8
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Authors
Abidi, F
Abidi, F E
Arena, F
Arena, J F
CHANG, S L
CLARKE, N A
Davis, D D
Ferdinand, J A
Howell, R R
KABLER, P W
Lubs, H A
Phelan, M C
Rogers, R C
STEVENSON, R E
Schroer, R J
Schwartz, C E
Simensen, R J
Skelly, J M
Stevenson, R E
Taylor, H A
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Topics
Abnormalities, Multiple
Adolescent
Adult
Child
Child, Preschool
Chromosome Mapping
Female
Genetic Linkage
Humans
Infant, Newborn
Intellectual Disability
Male
Middle Aged
Pedigree
Pregnancy
Syndrome
X Chromosome
abnormalities
diagnosis
genetics
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English
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61.
Quality control studies on fetal bovine serum used in tissue culture.
[electronic resource]
by
Boone, C W
Mantel, N
Caruso, T D
Kazam, E
Stevenson, R E
Producer:
19740502
In:
In vitro
vol. 7
Online resources:
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62.
Autism and macrocephaly.
[electronic resource]
by
Stevenson, R E
Schroer, R J
Skinner, C
Fender, D
Simensen, R J
Producer:
19970703
In:
Lancet (London, England)
vol. 349
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63.
Preventable fraction of mental retardation: analysis based on individuals with severe mental retardation.
[electronic resource]
by
Stevenson, R E
Massey, P S
Schroer, R J
McDermott, S
Richter, B
Producer:
19960822
In:
Mental retardation
vol. 34
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64.
Duplication of distal 19q: clinical report and review.
[electronic resource]
by
Boyd, E
Grass, F S
Parke, J C
Knutson, K
Stevenson, R E
Producer:
19920323
In:
American journal of medical genetics
vol. 42
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65.
Holmes-Gang syndrome is allelic with XLMR-hypotonic face syndrome.
[electronic resource]
by
Stevenson, R E
Abidi, F
Schwartz, C E
Lubs, H A
Holmes, L B
Producer:
20001107
In:
American journal of medical genetics
vol. 94
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66.
Mannosidosis: deficiency of a specific alpha-mannosidase component in cultured fibroblasts.
[electronic resource]
by
Taylor, H A
Thomas, G H
Aylsworth, A
Stevenson, R E
Reynolds, L W
Producer:
19750627
In:
Clinica chimica acta; international journal of clinical chemistry
vol. 59
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67.
Cognitive function in Coffin-Lowry syndrome.
[electronic resource]
by
Simensen, R J
Abidi, F
Collins, J S
Schwartz, C E
Stevenson, R E
Producer:
20030207
In:
Clinical genetics
vol. 61
Online resources:
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68.
Mannosidosis: deficiency of a specific alpha-mannosidase component in cultured fibroblasts.
[electronic resource]
by
Taylor, H A
Thomas, G H
Aylsworth, A
Stevenson, R E
Reynolds, L W
Producer:
19750627
In:
Clinica chimica acta; international journal of clinical chemistry
vol. 59
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69.
Allan-Herndon syndrome. II. Linkage to DNA markers in Xq21.
[electronic resource]
by
Schwartz, C E
Ulmer, J
Brown, A
Pancoast, I
Goodman, H O
Stevenson, R E
Producer:
19900928
In:
American journal of human genetics
vol. 47
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70.
Allelism, non-allelism and genetic compounds among the mucopolysaccharidoses: corrective factors in nosology, genetics and therapy.
[electronic resource]
by
McKusick, V A
Howell, R R
Hussels, I E
Neufeld, E F
Stevenson, R E
Producer:
19730628
In:
Transactions of the Association of American Physicians
vol. 85
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71.
Removal of Coxsackie and bacterial viruses in water by flocculation. II. Removal of Coxsackie and bacterial viruses and the native bacteria in raw Ohio River water by flocculation with aluminum sulfate and ferric chloride.
[electronic resource]
by
CHANG, S L
STEVENSON, R E
BRYANT, A R
WOODWARD, R L
KABLER, P W
Producer:
20000701
In:
American journal of public health and the nation's health
vol. 48
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72.
Fellowships and career development in dysmorphology and clinical genetics.
[electronic resource]
by
Graham, J M
Curry, C J
Hoyme, H E
Stevenson, R E
Hall, J G
Producer:
19920428
In:
Pediatric clinics of North America
vol. 39
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73.
Transport media for tissue specimens: a comparative study.
[electronic resource]
by
Potts, W E
Saul, R A
Riley, S E
Stevenson, R E
Taylor, H A
Producer:
19830923
In:
American journal of medical genetics
vol. 15
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74.
Removal of Coxsackie and bacterial viruses in water by flocculation. I. Removal of Coxsackie and bacterial viruses in water of known chemical content by flocculation with aluminum sulfate or ferric chloride under various testing conditions.
[electronic resource]
by
CHANG, S L
STEVENSON, R E
BRYANT, A R
WOODWARD, R L
KABLER, P W
Producer:
20000701
In:
American journal of public health and the nation's health
vol. 48
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75.
Hepatic adenomata with type 1 glycogen storage disease.
[electronic resource]
by
Howell, R R
Stevenson, R E
Ben-Menachem, Y
Phyliky, R L
Berry, D H
Producer:
19761101
In:
JAMA
vol. 236
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76.
Fragile X syndrome in South Carolina.
[electronic resource]
by
Saul, R A
Stevenson, R E
Simensen, R J
Wilkes, G
Alexander, W
Taylor, H
Producer:
19830107
In:
Journal of the South Carolina Medical Association (1975)
vol. 78
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77.
Allelism, non-allelism, and genetic compounds among the mucopolysaccharidoses.
[electronic resource]
by
McKusick, V A
Howell, R R
Hussels, I E
Neufeld, E F
Stevenson, R E
Producer:
19720708
In:
Lancet (London, England)
vol. 1
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78.
Non-syndromic X-linked mental retardation associated with a missense mutation (P312L) in the FGD1 gene.
[electronic resource]
by
Lebel, R R
May, M
Pouls, S
Lubs, H A
Stevenson, R E
Schwartz, C E
Producer:
20020819
In:
Clinical genetics
vol. 61
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79.
Deletion mapping of plasminogen activator inhibitor, type I (PLANH1) and beta-glucuronidase (GUSB) in 7q21----q22.
[electronic resource]
by
Schwartz, C E
Stanislovitis, P
Phelan, M C
Klinger, K
Taylor, H A
Stevenson, R E
Producer:
19910801
In:
Cytogenetics and cell genetics
vol. 56
Online resources:
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80.
Localization of branchio-oto-renal (BOR) syndrome to a 3 Mb region of chromosome 8q.
[electronic resource]
by
Wang, Y
Treat, K
Schroer, R J
O'Brien, J E
Stevenson, R E
Schwartz, C E
Producer:
19941018
In:
American journal of medical genetics
vol. 51
Online resources:
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