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1
De novo interstitial deletion of the long arm of chromosome 2: 46,XXX,del(2)(q14q21), associated with premature craniosynostosis
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De novo interstitial deletion of the long arm of chromosome 2: 46,XXX,del(2)(q14q21), associated with premature craniosynostosis

Annales de génétique, 1987, Vol.30 (1), p.33

ISSN: 0003-3995 ;PMID: 3498427

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2
Triploid (69, XXX) child having lived for 9 days
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Article
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Triploid (69, XXX) child having lived for 9 days

Annales de génétique, 1974-12, Vol.17 (4), p.283

ISSN: 0003-3995 ;PMID: 4548826

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3
A case of double trisomy: 48,XXX,18
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Article
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A case of double trisomy: 48,XXX,18

Annales de génétique, 1971-12, Vol.14 (4), p.301

ISSN: 0003-3995 ;PMID: 5316134

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4
Trisomy 18 and 47,XXX syndrome in the same sibship
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Article
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Trisomy 18 and 47,XXX syndrome in the same sibship

Annales de génétique, 1969-03, Vol.12 (1), p.59

ISSN: 0003-3995 ;PMID: 5306714

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5
Postnatal diagnosis and prognosis of 2 cases of triploidy
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Article
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Postnatal diagnosis and prognosis of 2 cases of triploidy

Archives de pédiatrie : organe officiel de la Société française de pédiatrie, 2010-07, Vol.17 (7), p.1078 [Peer Reviewed Journal]

Copyright (c) 2010 Elsevier Masson SAS. All rights reserved. ;EISSN: 1769-664X ;DOI: 10.1016/j.arcped.2010.03.009 ;PMID: 20444585

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6
Genetic analysis of Turner syndrome: 89 cases in Tunisia
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Article
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Genetic analysis of Turner syndrome: 89 cases in Tunisia

Annales d'endocrinologie, 2008-11, Vol.69 (5), p.440 [Peer Reviewed Journal]

ISSN: 0003-4266 ;DOI: 10.1016/j.ando.2008.01.007 ;PMID: 18541220

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7
Chronic osteoarticular pathology and school attendance
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Article
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Chronic osteoarticular pathology and school attendance

Archives françaises de pediatrie, 1979-12, Vol.36 Suppl 2, p.XXX

ISSN: 0003-9764 ;PMID: 161965

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  1. Peer-reviewed Journals (2)

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