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| Result Number | Material Type | Add to My Shelf Action | Record Details and Options |
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| 1 |
Material Type: Article
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Trisomy 18 or postnatal Edward´s syndrome: descriptive study conducted at the University Hospital Center of Casablanca and literature reviewThe Pan African medical journal, 2020, Vol.37, p.309-309 [Peer Reviewed Journal]Copyright: Fatima Zahra Outtaleb et al. ;EISSN: 1937-8688 ;DOI: 10.11604/pamj.2020.37.309.26205 ;PMID: 33654528Full text available |
| 2 |
Material Type: Article
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Caudal regression syndrome: about a caseThe Pan African medical journal, 2018, Vol.30, p.219-219 [Peer Reviewed Journal]EISSN: 1937-8688 ;DOI: 10.11604/pamj.2018.30.219.8691 ;PMID: 30574238Full text available |
| 3 |
Material Type: Article
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Rhombencephalosynapsis : a rare cerebellar malformation not to missRevue médicale de Liège, 2023-07, Vol.78 (7-8), p.407 [Peer Reviewed Journal]ISSN: 0370-629X ;PMID: 37560950Full text available |
| 4 |
Material Type: Article
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The long face syndromeOrthodontie française, 2016-12, Vol.87 (4), p.479-489 [Peer Reviewed Journal]EDP Sciences, SFODF, 2016. ;ISSN: 0078-6608 ;PMID: 27938659Full text available |
| 5 |
Material Type: Article
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Fraser syndrome: Case reportJournal francais d'ophtalmologie, 2018-12, Vol.41 (10), p.e489 [Peer Reviewed Journal]EISSN: 1773-0597 ;DOI: 10.1016/j.jfo.2018.04.006 ;PMID: 30446346Full text available |
| 6 |
Material Type: Article
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Toriello-Carey syndrome in a patient with a de novo balanced translocation [46,XY,t(2;14)(q33;q22)] interrupting SATB2Clinical genetics, 2009-03, Vol.75 (3), p.259-264 [Peer Reviewed Journal]2008 The Authors Journal compilation © 2008 Blackwell Munksgaard ;2009 INIST-CNRS ;Journal compilation © 2008 Blackwell Munksgaard ;ISSN: 0009-9163 ;EISSN: 1399-0004 ;DOI: 10.1111/j.1399-0004.2008.01145.x ;PMID: 19170718 ;CODEN: CLGNAYFull text available |
| 7 |
Material Type: Article
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Ophthalmological manifestations of 13q deletion syndrome: A case reportJournal francais d'ophtalmologie, 2019-05, Vol.42 (5), p.e219 [Peer Reviewed Journal]EISSN: 1773-0597 ;DOI: 10.1016/j.jfo.2018.11.004 ;PMID: 30955898Full text available |
| 8 |
Material Type: Article
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A rare cause of exertional dry cough: agenesis of the left pulmonary artery associated with pulmonary hypoplasiaThe Pan African medical journal, 2017, Vol.27, p.146-146 [Peer Reviewed Journal]EISSN: 1937-8688 ;DOI: 10.11604/pamj.2017.27.146.11399 ;PMID: 28904674Full text available |
| 9 |
Material Type: Article
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Lethal osteo-chondro-dysplasia: feto-pathological study of 32 casesTunisie Medicale, 2009-02, Vol.87 (2), p.127-132 [Peer Reviewed Journal]ISSN: 0041-4131 ;PMID: 19522446Full text available |
| 10 |
Material Type: Article
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Ocular coloboma and results of brain MRI: preliminary resultsJournal francais d'ophtalmologie, 2013-03, Vol.36 (3), p.210-220 [Peer Reviewed Journal]Copyright © 2012 Elsevier Masson SAS. All rights reserved. ;EISSN: 1773-0597 ;DOI: 10.1016/j.jfo.2012.02.014 ;PMID: 23177150Full text available |
| 11 |
Material Type: Article
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Embryotoxon in Axenfeld-Rieger syndrome in an infantJournal francais d'ophtalmologie, 2018-01, Vol.41 (1), p.100-101 [Peer Reviewed Journal]EISSN: 1773-0597 ;DOI: 10.1016/j.jfo.2017.08.004 ;PMID: 29241980Full text available |
| 12 |
Material Type: Article
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The Mayer-Rokitansky-Küster-Hauser (MRKH) syndrome: clinical description and geneticsJournal de gynécologie, obstétrique et biologie de la reproduction, 2008-10, Vol.37 (6), p.539-546ISSN: 0368-2315 ;DOI: 10.1016/j.jgyn.2008.07.002 ;PMID: 18723299Full text available |
| 13 |
Material Type: Article
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Amniotic bands syndrome and its diagnostic difficulties and management in Burkina FasoThe Pan African medical journal, 2015, Vol.20, p.208-208 [Peer Reviewed Journal]EISSN: 1937-8688 ;DOI: 10.11604/pamj.2015.20.208.6129 ;PMID: 26113939Full text available |
| 14 |
Material Type: Article
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Fanconi anemia: report of a new caseThe Pan African medical journal, 2015, Vol.20, p.92-92 [Peer Reviewed Journal]EISSN: 1937-8688 ;DOI: 10.11604/pamj.2015.20.92.6116 ;PMID: 26213593Full text available |
| 15 |
Material Type: Article
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Connecting isolated congenital asplenia to the ribosomeBiologie aujourd'hui, 2014, Vol.208 (4), p.289 [Peer Reviewed Journal]Société de Biologie, 2015. ;EISSN: 2105-0686 ;PMID: 25840456Full text available |
| 16 |
Material Type: Article
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Genetic complexity of ciliopathies and novel genes identificationM.S. Médecine sciences, 2014-11, Vol.30 (11), p.1011-1023 [Peer Reviewed Journal]2014 médecine/sciences – Inserm. ;ISSN: 0767-0974 ;EISSN: 1958-5381 ;DOI: 10.1051/medsci/20143011016 ;PMID: 25388584Full text available |
| 17 |
Material Type: Article
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Congenital diaphragmatic hernia - mechanisms of pulmonary hypoplasiaRevue des maladies respiratoires, 2011-04, Vol.28 (4), p.463-474 [Peer Reviewed Journal]Distributed under a Creative Commons Attribution 4.0 International License ;ISSN: 0761-8425 ;EISSN: 1776-2588 ;DOI: 10.1016/j.rmr.2010.10.032 ;PMID: 21549902Full text available |
| 18 |
Material Type: Article
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Poland syndromeThe Pan African medical journal, 2015, Vol.22, p.124-124 [Peer Reviewed Journal]EISSN: 1937-8688 ;DOI: 10.11604/pamj.2015.22.124.7972 ;PMID: 26889305Full text available |
| 19 |
Material Type: Article
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Hyalinosis cutis et mucosae : 5 cases from Tabarka (Tunisia)Tunisie Medicale, 2011-05, Vol.89 (5), p.485-490 [Peer Reviewed Journal]ISSN: 0041-4131 ;PMID: 21557189Full text available |
| 20 |
Material Type: Article
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Spondylocostal dysostosis: a rare genetic diseaseRevue médicale de Liège, 2004-09, Vol.59 (9), p.513-516 [Peer Reviewed Journal]ISSN: 0370-629X ;PMID: 15562550Full text available |
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