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Hennekam, Raoul CM
360
results:
Search for persons
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Format
Online (360)
Mediatypes
Articles (Online) (338)
Bookchapter (Online) (4)
OpenAccess-fulltext (18)
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?
1
Laminopathies: clinical presentations and management:
Hennekam, Raoul CM
Orphanet Journal of Rare Diseases. 10 (2015) Suppl 2 - p. O23 , 2015
Link:
https://doi.org/10.1186/..
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2
The persistent embryonic vein in Klippel–Trenaunay syndrome:
Oduber, Charlène EU
;
Young-Afat, Danny A
;
van der Wal, Allard C
...
Vascular Medicine. 18 (2013) 4 - p. 185-191 , 2013
Link:
https://doi.org/10.1177/..
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3
Non‐immune hydrops fetalis: A short review of etiology and ..:
Bellini, Carlo
;
Hennekam, Raoul CM
American Journal of Medical Genetics Part A. 158A (2012) 3 - p. 597-605 , 2012
Link:
https://doi.org/10.1002/..
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4
Delineation and Diagnostic Criteria of Oral-Facial-Digital ..:
Poretti, Andrea
;
Vitiello, Giuseppina
;
Hennekam, Raoul CM
...
Orphanet Journal of Rare Diseases. 7 (2012) 1 - p. , 2012
Link:
https://doi.org/10.1186/..
?
5
Care for patients with ultra-rare disorders:
Hennekam, Raoul CM.
European Journal of Medical Genetics. 54 (2011) 3 - p. 220-224 , 2011
Link:
https://doi.org/10.1016/..
?
6
Very rare disorders - organisation of care:
Hennekam, Raoul CM
Orphanet Journal of Rare Diseases. 5 (2010) S1 - p. , 2010
Link:
https://doi.org/10.1186/..
?
7
Diabetes mellitus, exocrine pancreatic deficiency, hypertri..:
Hussain, Khalid
;
Padidela, Raja
;
Kapoor, Ritika R
...
Pediatric Diabetes. 10 (2009) 3 - p. 193-197 , 2009
Link:
https://doi.org/10.1111/..
?
8
Arteriovenous and lymphatic malformations, linear verrucous..:
Hennekam, Raoul CM.
;
Kwa, Vincent I. H.
;
van Amerongen, Arlette
Clinical Dysmorphology. 5 (1999) 2 - p. 111???116 , 1999
Link:
https://doi.org/10.1097/..
?
9
European lipodystrophy registry: background and structure:
von Schnurbein, Julia
;
Adams, Claire
;
Akinci, Baris
...
doi:10.17863/CAM.50982. , 2020
Link:
https://doi.org/10.17863..
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10
Laminopathies: clinical presentations and management:
Hennekam, Raoul CM
http://www.ojrd.com/content/10/S2/O23. , 2015
Link:
http://www.ojrd.com/cont..
?
11
De Novo Mutations in NALCN Cause a Syndrome Characterized b..:
Chong, Jessica X
;
McMillin, Margaret J
;
Shively, Kathryn M
...
qt59c5b36g. , 2015
Link:
https://escholarship.org..
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12
Next Generation Sequencing Demands Next Generation Phenotyp..:
Hennekam, Raoul CM
;
Biesecker, Leslie G
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3327792. , 2012
Link:
http://www.ncbi.nlm.nih...
?
13
Delineation and Diagnostic Criteria of Oral-Facial-Digital ..:
Poretti, Andrea
;
Vitiello, Giuseppina
;
Hennekam, Raoul CM
...
http://www.ojrd.com/content/7/1/4. , 2012
Link:
http://www.ojrd.com/cont..
?
14
Delineation and Diagnostic Criteria of Oral-Facial-Digital ..:
Poretti Andrea
;
Vitiello Giuseppina
;
Hennekam Raoul CM
...
http://www.ojrd.com/content/7/1/4. , 2012
Link:
https://doi.org/10.1186/..
?
15
Mutation Update for the PORCN Gene:
Lombardi, Maria Paola
;
Hennekam, Raoul CM
;
Bulk, Saskia
...
info:eu-repo/semantics/altIdentifier/doi/10.1002/humu.21505. , 2011
Link:
https://hal.archives-ouv..
1-15