E-LIB Suche - Ergebnisse für: Hennekam, R

1

Towards an astrochronological framework for the lower Paleo..:

Lantink, M.L. ; Davies, J.H.F.L. ; Hennekam, R....
South African Journal of Geology. 127 (2024) 2 - p. 325-358 , 2024

Link: https://doi.org/10.25131..

2

Effects of redox variability and early diagenesis on marine..:

Frieling, J. ; Mather, T.A. ; März, C....
Geochimica et Cosmochimica Acta. 351 (2023) - p. 78-95 , 2023

Link: https://doi.org/10.1016/..

3

Suborbital Hydrological Variability Inferred From Coupled B..:

Le Houedec, S. ; Mojtahid, M. ; Bicchi, E...
Paleoceanography and Paleoclimatology. 35 (2020) 2 - p. , 2020

Link: https://doi.org/10.1029/..

4

Evaluation and application of foraminiferal element/calcium..:

Mojtahid, M. ; Hennekam, R. ; De Nooijer, L....
Marine Micropaleontology. 153 (2019) - p. 101783 , 2019

Link: https://doi.org/10.1016/..

5

Refining the phenotypical and mutational spectrum of Taybi‐..:

Putoux, A. ; Alqahtani, A. ; Pinson, L....
Clinical Genetics. 90 (2016) 6 - p. 550-555 , 2016

Link: https://doi.org/10.1111/..

6

Osteopathia striata congenita with cranial sclerosis and in..:

Holman, SK ; Morgan, T ; Baujat, G...
Clinical Genetics. 83 (2013) 3 - p. 251-256 , 2013

Link: https://doi.org/10.1111/..

7

SporadicCOL4A1mutations with extensive prenatal porencephal..:

Meuwissen, M.E.C. ; de Vries, L.S. ; Verbeek, H.A....
Neurology. 76 (2011) 9 - p. 844-846 , 2011

Link: https://doi.org/10.1212/..

8

Simultaneous analysis of the behavioural phenotype, physica..:

Wulffaert, J. ; van Berckelaer‐Onnes, I. ; Kroonenberg, P....
Journal of Intellectual Disability Research. 53 (2009) 7 - p. 604-619 , 2009

Link: https://doi.org/10.1111/..

9

Prevalence of RIB anomalies in normal caucasian children an..:

MERKS, J ; SMETS, A ; VANRIJN, R...
Annales de G�n�tique. , 2004

Link: https://doi.org/10.1016/..

10

Mutation analysis of the MKKS gene in McKusick-Kaufman synd..:

Slavotinek, A. ; Searby, C. ; Al-Gazali, L....
Human Genetics. 110 (2002) 6 - p. 561-567 , 2002

Link: https://doi.org/10.1007/..

11

Andersen-Tawil syndrome: Overlapping clinical features with..:

van der Werf - 't Lam, A.S. ; van Haeringen, A. ; Rinnen, T....
European Journal of Medical Genetics. 65 (2022) 1 - p. 104382 , 2022

Link: https://doi.org/10.1016/..

12

Dermatological signs lead to discovery of mosaicACTBvariant..:

Polubothu, S. ; Abdin, D. ; Barysch, M....
British Journal of Dermatology. 183 (2020) 6 - p. 1128-1130 , 2020

Link: https://doi.org/10.1111/..

13

Awake Flexible Fiberoptic Laryngoscopy to diagnose glossopt..:

Basart, H. ; König, A.M. ; Bretschneider, J.H....
Clinical Otolaryngology. 41 (2016) 5 - p. 467-471 , 2016

Link: https://doi.org/10.1111/..

14

A de novo mutation in ZMYND11, a candidate gene for 10p15.3..:

Cobben, J.M. ; Weiss, M.M. ; van Dijk, F.S....
European Journal of Medical Genetics. 57 (2014) 11-12 - p. 636-638 , 2014

Link: https://doi.org/10.1016/..

15

The IGSF1 Deficiency Syndrome: Characteristics of Male and ..:

Joustra, S. D. ; Schoenmakers, N. ; Persani, L....
The Journal of Clinical Endocrinology & Metabolism. 98 (2013) 12 - p. 4942-4952 , 2013

Link: https://doi.org/10.1210/..