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Results of search for 'au:"LADDA, R"', page 3 of 5
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Authors
Aikawa, M
Arnold, J
Atkins, L
Barritault, D
Chua, C C
Dobelle, Y
Eyster, M E
Frankel, C A
Geder, L
Geiman, D E
Kasat, Vo
Keller, G H
Kreider, J W
Ladda, R
Ladda, R L
Mowrey, P N
Ramer, J C
Rapp, F
Rogan, P K
Towfighi, J
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Abnormalities, Multiple
Adult
Animals
Child, Preschool
Female
Fibroblasts
Humans
Infant
Infant, Newborn
Karyotyping
Male
Mice
Pedigree
Rats
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abnormalities
analysis
genetics
metabolism
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Your search returned 93 results.
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41.
Hypothyroidism in an infant with Down's syndrome.
[electronic resource]
by
King, S L
Ladda, R L
Kulin, H E
Producer:
19780321
In:
American journal of diseases of children (1960)
vol. 132
Online resources:
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42.
Multiple pterygium syndrome. An overview.
[electronic resource]
by
Ramer, J C
Ladda, R L
Demuth, W W
Producer:
19880728
In:
American journal of diseases of children (1960)
vol. 142
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43.
Hereditary multiple exostoses: report of a kindred.
[electronic resource]
by
Gordon, S L
Buchanan, J R
Ladda, R L
Producer:
19820521
In:
Journal of medical genetics
vol. 18
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44.
Carriers with excessively low factor VIII procoagulant activity (VIII AHF): a study of two unrelated families with mild hemophilia A.
[electronic resource]
by
Eyster, M E
Ladda, R L
Bowman, H S
Producer:
19770520
In:
Blood
vol. 49
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45.
Detection of an Mr 200,000 glycoprotein in the culture medium of skin fibroblasts from patients with Huntington disease.
[electronic resource]
by
Chua, C C
Geiman, D E
Ladda, R L
Producer:
19830505
In:
Biochemical and biophysical research communications
vol. 111
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46.
Marden-Walker phenotype: spectrum of variability in three infants.
[electronic resource]
by
Ramer, J C
Frankel, C A
Ladda, R L
Producer:
19930317
In:
American journal of medical genetics
vol. 45
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47.
Cerebro-ocular dysplasia-muscular dystrophy (COD-MD) syndrome.
[electronic resource]
by
Towfighi, J
Sassani, J W
Suzuki, K
Ladda, R L
Producer:
19850311
In:
Acta neuropathologica
vol. 65
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48.
Cytogenetic engineering in vivo: restoration of biologic complement activity to C5-deficient mice by intravenous inoculation of hybrid cells.
[electronic resource]
by
Levy, N L
Synderman, R
Ladda, R L
Lieberman, R
Producer:
19740522
In:
Proceedings of the National Academy of Sciences of the United States of America
vol. 70
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49.
Absence of membrane-bound elementary particles following negative staining of a respiratory-deficient (p - ) strain of baker's yeast.
[electronic resource]
by
Bachop, W
Boatman, E S
Mackler, B
Ladda, R L
Producer:
19720628
In:
Transactions of the American Microscopical Society
vol. 91
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50.
Somatic cell mosaicism: another source of phenotypic heterogeneity in nuclear families with osteogenesis imperfecta.
[electronic resource]
by
Constantinou-Deltas, C D
Ladda, R L
Prockop, D J
Producer:
19930422
In:
American journal of medical genetics
vol. 45
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51.
Reservoir complete denture in a patient with xerostomia secondary to radiotherapy for oral carcinoma: a case report and review of literature.
[electronic resource]
by
Ladda, R
Kasat, Vo
Gangadhar, Sa
Baheti, S
Bhandari, Aj
Producer:
20140424
In:
Annals of medical and health sciences research
vol. 4
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52.
Radioreceptor assay for epidermal growth factor.
[electronic resource]
by
Ladda, R L
Bullock, L P
Gianopoulos, T
McCormick, L
Producer:
19790925
In:
Analytical biochemistry
vol. 93
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53.
Chromosomal mosaicism in Down's syndrome: a diagnostic challenge.
[electronic resource]
by
Ladda, R L
Maisels, M J
Dossett, J H
Dobelle, Y
Producer:
19771229
In:
Developmental medicine and child neurology
vol. 19
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54.
Craniosynostosis associated with limb reduction malformations and cleft lip/palate: a distinct syndrome.
[electronic resource]
by
Ladda, R L
Stoltzfus, E
Gordon, S L
Graham, W P
Producer:
19861117
In:
Pediatrics
vol. 61
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55.
Acute diphenylhydantoin intoxication.
[electronic resource]
by
Tenckhoff, H
Sherrard, D J
Hickman, R O
Ladda, R L
Producer:
19690108
In:
American journal of diseases of children (1960)
vol. 116
Online resources:
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56.
"Marden-Walker syndrome": neuropathologic findings in two siblings.
[electronic resource]
by
Sees, J N
Towfighi, J
Robins, D B
Ladda, R L
Producer:
19901204
In:
Pediatric pathology
vol. 10
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57.
Computer-assisted analysis of chromosomal abnormalities: detection of a deletion in aniridia-Wilms' tumor syndrome.
[electronic resource]
by
Ladda, R
Atkins, L
Littlefield, J
Neurath, P
Marimuthu, K M
Producer:
19740928
In:
Science (New York, N.Y.)
vol. 185
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58.
An approach to a genetic eye disorder.
[electronic resource]
by
Rabinowitz, Y S
Sassani, J W
Ladda, R
Eyster, M E
Producer:
19890928
In:
Transactions - Pennsylvania Academy of Ophthalmology and Otolaryngology
vol. 40
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59.
A review of phenotype-karyotype correlations in individuals with interstitial deletions of the long arm of chromosome 2.
[electronic resource]
by
Ramer, J C
Ladda, R L
Frankel, C A
Beckford, A
Producer:
19890630
In:
American journal of medical genetics
vol. 32
Online resources:
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60.
Induction and suppression of type I collagenase in cultured human cells.
[electronic resource]
by
Chua, C C
Barritault, D
Geiman, D E
Ladda, R L
Producer:
19871216
In:
Collagen and related research
vol. 7
Online resources:
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