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Results of search for 'su:"Syndrome"', page 4 of 28953
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Authors
Ackerman, Michael J
Brown, P
Cohen, J
Cohen, M M
Fauci, A S
Fryns, J P
Gajdusek, D C
Gallo, R C
Moutsopoulos, H M
Nakamura, Y
Opitz, J M
Sato, T
Shoenfeld, Y
Suzuki, T
Suzuki, Y
Takahashi, K
Takahashi, M
Tanaka, K
Tanaka, M
Wechsler, B
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Topics
Acquired Immunodeficiency Syndrome
Adolescent
Adult
Aged
Animals
Child
Female
Humans
Male
Middle Aged
Syndrome
adverse effects
blood
complications
diagnosis
drug therapy
etiology
genetics
metabolism
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61.
[Progeroid syndrome with Ehlers-Danlos features].
[electronic resource]
by
Izumikawa, Y
Producer:
20011211
In:
Ryoikibetsu shokogun shirizu
no. 34 Pt 2
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62.
[Hulushi-Behçet syndrome; clinical manifestations and their relation to ectodermosis erosiva pluriorificialis].
[electronic resource]
by
VOGLINO, A
Producer:
20030501
In:
Minerva dermatologica
vol. 27
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63.
Sneddon's syndrome: additional neurological feature in antiphospholipid (Hughes') syndrome.
[electronic resource]
by
Sinharay, R
Producer:
20031120
In:
Postgraduate medical journal
vol. 79
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64.
CHROMOSOMAL ABNORMALITIES IN HUMAN DISEASE.
[electronic resource]
by
TURNER, B
Producer:
19961201
In:
Bulletin of the Post-Graduate Committee in Medicine, University of Sydney
vol. 19
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65.
THE ROLE OF DERMATOGLYPHICS IN MEDICAL BIOLOGY.
[electronic resource]
by
HOLT, S B
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19961201
In:
Medical world
vol. 101
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66.
[Rare hyperimmunoglobulinemia E syndromes].
[electronic resource]
by
Katchourine, I
Pradalier, A
Producer:
19981029
In:
La Revue de medecine interne
vol. 19
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67.
[CHROMOSOME-RELATED PRIMARY TESTICULAR LESIONS].
[electronic resource]
by
NIERMANN, H
Producer:
19961201
In:
Archiv fur klinische und experimentelle Dermatologie
vol. 219
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68.
Pigmentary anomalies and hearing loss.
[electronic resource]
by
Toriello, Helga V
Producer:
20110531
In:
Advances in oto-rhino-laryngology
vol. 70
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69.
Neuropathology of mitochondrial encephalomyopathies due to mitochondrial DNA defects.
[electronic resource]
by
Sparaco, M
Bonilla, E
DiMauro, S
Powers, J M
Producer:
19930302
In:
Journal of neuropathology and experimental neurology
vol. 52
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70.
Syndromes of hearing loss associated with visual loss.
[electronic resource]
by
Abou-Elhamd, Kamal Ahmed
ElToukhy, Hesham Mohamed
Al-Wadaani, Fahad Abdullah
Producer:
20141029
In:
European archives of oto-rhino-laryngology : official journal of the European Federation of Oto-Rhino-Laryngological Societies (EUFOS) : affiliated with the German Society for Oto-Rhino-Laryngology - Head and Neck Surgery
vol. 271
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71.
[Association of Vogt-Koyanagi disease, Gougerot-Sjögren syndrome and erythema nodosum].
[electronic resource]
by
Gouet, D
Anquez, M
Risse, J F
Becq-Giraudon, B
Producer:
19860311
In:
Presse medicale (Paris, France : 1983)
vol. 13
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72.
The contribution of constitutional chromosomal abnormalities to mental deficiency.
[electronic resource]
by
Baikie, A G
Garson, O M
Weste, S M
Producer:
19690401
In:
Proceedings of the Australian Association of Neurologists
vol. 5
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73.
Cowden syndrome.
[electronic resource]
by
Gustafson, Shanna
Zbuk, Kevin M
Scacheri, Cheryl
Eng, Charis
Producer:
20071119
In:
Seminars in oncology
vol. 34
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74.
Haemorrhagic fever with renal syndrome, virological and epidemiological aspects.
[electronic resource]
by
Niklasson, B S
Producer:
19920601
In:
Pediatric nephrology (Berlin, Germany)
vol. 6
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75.
CHROMOSOMES AND HUMAN DISEASE.
[electronic resource]
by
MILLER, W V
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19961201
In:
Missouri medicine
vol. 61
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76.
Severe congenital myopathy with Möbius, Robin, and Poland sequences: new aspects of the Carey-Fineman-Ziter syndrome.
[electronic resource]
by
Dufke, Andreas
Riethmüller, Joachim
Enders, Herbert
Producer:
20050222
In:
American journal of medical genetics. Part A
vol. 127A
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77.
People with intellectual disability: what do we know about adulthood and life expectancy?
[electronic resource]
by
Coppus, A M W
Producer:
20140324
In:
Developmental disabilities research reviews
vol. 18
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78.
Atrioventricular canal defect without Down syndrome: a heterogeneous malformation.
[electronic resource]
by
Digilio, M C
Marino, B
Toscano, A
Giannotti, A
Dallapiccola, B
Producer:
19990930
In:
American journal of medical genetics
vol. 85
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79.
Constitutional chromosome abnormalities among patients referred for blood karyotype analysis: a 5-year study at the AUBMC.
[electronic resource]
by
Mahfouz, R
al-Oreibi, G
Darwiche, N
el-Khechen, S
Zahed, L
Producer:
20020416
In:
Le Journal medical libanais. The Lebanese medical journal
vol. 49
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80.
Radiographic clues to cytogenetic disease.
[electronic resource]
by
O'Hara, A E
Abram, S E
Producer:
19720110
In:
Texas medicine
vol. 67
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