R.C. Hennekam : rechercher sur Z-Library

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1

Sexual Harassment in the Creative Industries: Tolerance, Culture and the Need for Change

Hennekam, Sophie, Bennett, Dawn

Journal:

Gender, Work & Organization

Année:

2017

Langue:

english

Fichier:

PDF, 216 KB

english, 2017

2

Hereditary hemorrhagic telangiectasia:ENGandALK-1mutations in Dutch patients

T. G. W. Letteboer, R. A. Zewald, E. J. Kamping, G. de Haas, J. J. Mager, R. J. Snijder, D. Lindhout, F. A. M. Hennekam, C. J. J. Westermann, J. K. Ploos van Amstel

Journal:

Année:

2005

Langue:

english

Fichier:

PDF, 309 KB

english, 2005

3

Gender equality in employment in Saudi Arabia: a relational perspective

Syed, Jawad, Ali, Faiza, Hennekam, Sophie

Journal:

Career Development International

Année:

2018

Langue:

english

Fichier:

PDF, 212 KB

english, 2018

4

Career success of older workers: the influence of social skills and continuous learning ability

Hennekam, Sophie

Journal:

Journal of Management Development

Année:

2015

Langue:

english

Fichier:

PDF, 254 KB

english, 2015

5

Institutional racism in the film industry: a multilevel perspective

Hennekam, Sophie, Syed, Jawad

Journal:

Equality Diversity and Inclusion An International Journal

Année:

2018

Langue:

english

Fichier:

PDF, 272 KB

english, 2018

6

Elements of morphology: Standard terminology for the external genitalia

Hennekam, Raoul C.M., Allanson, Judith E., Biesecker, Leslie G., Carey, John C., Opitz, John M., Vilain, Eric

Journal:

American Journal of Medical Genetics Part A

Année:

2013

Langue:

english

Fichier:

PDF, 5.77 MB

english, 2013

7

Determination of F r and K d from the solution of the equation of motion of a cyclist

Hennekam, W, Bontsema, J

Journal:

European Journal of Physics

Année:

1991

Langue:

english

Fichier:

PDF, 283 KB

english, 1991

8

Recurrent FXYD2 p.Gly41Arg mutation in patients with isolated dominant hypomagnesaemia

de Baaij, J. H. F., Dorresteijn, E. M., Hennekam, E. A. M., Kamsteeg, E.-J., Meijer, R., Dahan, K., Muller, M., van den Dorpel, M. A., Bindels, R. J. M., Hoenderop, J. G. J., Devuyst, O., Knoers, N. V

Journal:

Nephrology Dialysis Transplantation

Année:

2015

Langue:

english

Fichier:

PDF, 304 KB

english, 2015

9

Hiding gender: How female composers manage gender identity

Bennett, Dawn, Hennekam, Sophie, Macarthur, Sally, Hope, Cat, Goh, Talisha

Journal:

Journal of Vocational Behavior

Année:

2018

Langue:

english

Fichier:

PDF, 2.06 MB

english, 2018

10

Revised diagnostic criteria for the Marfan syndrome

De Paepe, Anne, Devereux, Richard B., Dietz, Harry C., Hennekam, Raoul C. M., Pyeritz, Reed E.

Journal:

American Journal of Medical Genetics

Année:

1996

Langue:

english

Fichier:

PDF, 955 KB

english, 1996

11

Congenital anomalies in the teratological collection of Museum Vrolik in Amsterdam, The Netherlands. II: Skeletal dysplasias

Oostra, Roelof-Jan, Baljet, Bob, Dijkstra, Piet F., Hennekam, Raoul C.M.

Journal:

American Journal of Medical Genetics

Année:

1998

Langue:

english

Fichier:

PDF, 1.86 MB

english, 1998

12

Non-immune hydrops fetalis: A short review of etiology and pathophysiology

Carlo Bellini, Raoul CM Hennekam

Journal:

American Journal of Medical Genetics Part A

Année:

2012

Langue:

english

Fichier:

PDF, 431 KB

english, 2012

13

Morphological Features in Children with Autism Spectrum Disorders: A Matched Case–Control Study

Heval Ozgen, Gerhard S. Hellemann, Rebecca K. Stellato, Bertine Lahuis, Emma van Daalen, Wouter G. Staal, Marije Rozendal, Raoul C. Hennekam, Frits A. Beemer, Herman van Engeland

Journal:

Journal of Autism and Developmental Disorders

Année:

2011

Langue:

english

Fichier:

PDF, 253 KB

english, 2011

14

Development and behaviour in Marshall–Smith syndrome: an exploratory study of cognition, phenotype and autism

I. D. C. van Balkom, A. Shaw, P. J. Vuijk, M. Franssens, H. W. Hoek, R. C. M. Hennekam

Journal:

Journal of Intellectual Disability Research

Année:

2011

Langue:

english

Fichier:

PDF, 308 KB

english, 2011

15

Challenges of older self-employed workers in creative industries

David Pick, Dr Paull Weber, Profess, Dr, Hennekam, Sophie

Journal:

Management Decision

Année:

2015

Langue:

english

Fichier:

PDF, 216 KB

english, 2015

16

Phenotype and natural history in 101 individuals with Pitt-Hopkins syndrome through an internet questionnaire system

de Winter, Channa F., Baas, Melanie, Bijlsma, Emilia K., van Heukelingen, John, Routledge, Sue, Hennekam, Raoul C. M.

Journal:

Orphanet Journal of Rare Diseases

Année:

2016

Langue:

english

Fichier:

PDF, 963 KB

english, 2016

17

Progress toward Understanding Vascular Malformations

Breugem, Corstiaan C., van der Horst, Chantal M. A. M., Hennekam, Raoul C. M.

Journal:

Plastic & Reconstructive Surgery

Année:

2001

Fichier:

PDF, 13.88 MB

2001

18

Contextualising diversity management in the Middle East and North Africa: a relational perspective

Hennekam, Sophie, Tahssain-Gay, Loubna, Syed, Jawad

Journal:

Human Resource Management Journal

Année:

2017

Langue:

english

Fichier:

PDF, 521 KB

english, 2017

19

Self-authorship and creative industries workers’ career decision-making

Bennett, Dawn, Hennekam, Sophie

Journal:

Human Relations

Année:

2018

Langue:

english

Fichier:

PDF, 361 KB

english, 2018

20

The Rise and Fall, and the Rise (Again) of Feminist Research in Music: ‘What Goes Around Comes Around’

Macarthur, Sally, Bennett, Dawn, Goh, Talisha, Hennekam, Sophie, Hope, Cat

Journal:

Musicology Australia

Année:

2017

Langue:

english

Fichier:

PDF, 595 KB

english, 2017

21

Creating a career as a woman composer: Implications for music in higher education

Bennett, Dawn, Macarthur, Sally, Hope, Cat, Goh, Talisha, Hennekam, Sophie

Journal:

British Journal of Music Education

Année:

2018

Langue:

english

Fichier:

PDF, 155 KB

english, 2018

22

When Can a Disability Quota System Empower Disabled Individuals in the Workplace? The Case of France

Richard, Sarah, Hennekam, Sophie

Journal:

Work Employment & Society

Année:

2020

Fichier:

PDF, 106 KB

2020

23

Tandem duplication of 11p12-p13 in a child with borderline development delay and eye abnormalities: Dose effect of the PAX6 gene product?

Aalfs, C. M., Fantes, J. A., Wenniger-Prick, L. J. J. M., Sluijter, S., Hennekam, R. C. M., van Heyningen, V., Hoovers, J. M. N.

Journal:

American Journal of Medical Genetics

Année:

1997

Langue:

english

Fichier:

PDF, 269 KB

english, 1997

24

Congenital anomalies in the teratological collection of Museum Vrolik in Amsterdam, The Netherlands. I: Syndromes with multiple congenital anomalies

Oostra, Roelof-Jan, Baljet, Bob, Dijkstra, Piet F., Hennekam, Raoul C.M.

Journal:

American Journal of Medical Genetics

Année:

1998

Langue:

english

Fichier:

PDF, 1.61 MB

english, 1998

25

Congenital anomalies in the teratological collection of museum Vrolik in Amsterdam, the Netherlands. iii: primary field defects, sequences, and other complex anomalies

Oostra, Roelof-Jan, Baljet, Bob, Verbeeten, Ben W.J.M., Hennekam, Raoul C.M.

Journal:

American Journal of Medical Genetics

Année:

1998

Langue:

english

Fichier:

PDF, 1.14 MB

english, 1998

26

Further delineation of the chromosome 14q terminal deletion syndrome

Clara D.M. van Karnebeek, Safira Quik, Sigrid Sluijter, Miriam M.F. Hulsbeek, Jan M.N. Hoovers, Raoul C.M. Hennekam

Journal:

American Journal of Medical Genetics Part A

Année:

2002

Langue:

english

Fichier:

PDF, 133 KB

english, 2002

27

Malformations of the axial skeleton in the museum Vrolik: II: Craniosynostoses and suture-related conditions

Roelof-Jan Oostra, Sander van der Wolk, Mario Maas, Raoul C.M. Hennekam

Journal:

American Journal of Medical Genetics Part A

Année:

2005

Langue:

english

Fichier:

PDF, 808 KB

english, 2005

28

Plantar lipomatosis, unusual facies, and developmental delay: Confirmation of Pierpont syndrome

Grétel G. Oudesluijs, Roel Hordijk, Maartje Boon, Paul E. Sijens, Raoul C.M. Hennekam

Journal:

American Journal of Medical Genetics Part A

Année:

2005

Langue:

english

Fichier:

PDF, 202 KB

english, 2005

29

Elements of morphology: Standard terminology for the nose and philtrum

Raoul C.M. Hennekam, Valerie Cormier-Daire, Judith G. Hall, Károly Méhes, Michael Patton, Roger E. Stevenson

Journal:

American Journal of Medical Genetics Part A

Année:

2009

Langue:

english

Fichier:

PDF, 885 KB

english, 2009

30

Elements of morphology: Introduction

Judith E. Allanson, Leslie G. Biesecker, John C. Carey, Raoul C.M. Hennekam

Journal:

American Journal of Medical Genetics Part A

Année:

2009

Langue:

english

Fichier:

PDF, 152 KB

english, 2009

31

Co-occurrence of severe Goltz–Gorlin syndrome and pentalogy of Cantrell – Case report and review of the literature

Robert Smigiel, Aleksandra Jakubiak, Maria Paola Lombardi, Wojciech Jaworski, Ryszard Slezak, Dariusz Patkowski, Raoul C. Hennekam

Journal:

American Journal of Medical Genetics Part A

Année:

2011

Langue:

english

Fichier:

PDF, 135 KB

english, 2011

32

Rett syndrome: A study of the face

Judith E. Allanson, Raoul C.M. Hennekam, Ute Moog, Eric E. Smeets

Journal:

American Journal of Medical Genetics Part A

Année:

2011

Langue:

english

Fichier:

PDF, 915 KB

english, 2011

33

Enzymatic hydrolysis of beer brewers' spent grain and the influence of pretreatments

G. Beldman, J. Hennekam, A. G. J. Voragen

Journal:

Biotechnology and Bioengineering

Année:

1987

Langue:

english

Fichier:

PDF, 364 KB

english, 1987

34

A family with severe X-linked arthrogryposis

R. C. M. Hennekam, P. G. Barth, W. Van Lookeren Campagne, M. De Visser, K. P. Dingemans

Journal:

European Journal of Pediatrics

Année:

1991

Langue:

english

Fichier:

PDF, 1.18 MB

english, 1991

35

Growth charts for children with Ellis–van Creveld syndrome

Sabine Verbeek, Paul H. C. Eilers, Kate Lawrence, Raoul C. M. Hennekam, Florens G. A. Versteegh

Journal:

European Journal of Pediatrics

Année:

2011

Langue:

english

Fichier:

PDF, 275 KB

english, 2011

36

A double hit implicates DIAPH3 as an autism risk gene

Vorstman, J A S, van Daalen, E, Jalali, G R, Schmidt, E R E, Pasterkamp, R J, de Jonge, M, Hennekam, E A M, Janson, E, Staal, W G, van der Zwaag, B

Journal:

Molecular Psychiatry

Année:

2010

Langue:

english

Fichier:

PDF, 588 KB

english, 2010

37

Germline KRAS and BRAF mutations in cardio-facio-cutaneous syndrome

Niihori, Tetsuya, Aoki, Yoko, Narumi, Yoko, Neri, Giovanni, Cavé, Hélène, Verloes, Alain, Okamoto, Nobuhiko, Hennekam, Raoul C M, Gillessen-Kaesbach, Gabriele, Wieczorek, Dagmar

Journal:

Nature Genetics

Année:

2006

Langue:

english

Fichier:

PDF, 219 KB

english, 2006

38

Standard terminology for phenotypic variations: The Elements of Morphology project, its current progress, and future directions

John C. Carey, Judith E. Allanson, Raoul C.M. Hennekam, Leslie G. Biesecker

Journal:

Année:

2012

Langue:

english

Fichier:

PDF, 410 KB

english, 2012

39

Cantú Syndrome Is Caused by Mutations in ABCC9

Bregje W.M. van Bon, Christian Gilissen, Dorothy K. Grange, Raoul C.M. Hennekam, Hülya Kayserili, Hartmut Engels, Heiko Reutter, John R. Ostergaard, Eva Morava, Konstantinos Tsiakas, Bertrand Isidor,

Journal:

The American Journal of Human Genetics

Année:

2012

Langue:

english

Fichier:

PDF, 356 KB

english, 2012

40

The Peters’ plus syndrome: a review

Liesbeth J.J.M. Maillette de Buy Wenniger-Prick, Raoul C.M. Hennekam

Journal:

Annales de Génétique

Année:

2002

Langue:

english

Fichier:

PDF, 435 KB

english, 2002

41

Delineation and Diagnostic Criteria of Oral-Facial-Digital Syndrome Type VI

Andrea Poretti, Giuseppina Vitiello, Raoul CM Hennekam, Filippo Arrigoni, Enrico Bertini, Renato Borgatti, Francesco Brancati, Stefano D’Arrigo, Francesca Faravelli, Lucio Giordano, Thierry AGM Huisma

Journal:

Orphanet Journal of Rare Diseases

Année:

2012

Langue:

english

Fichier:

PDF, 1.27 MB

english, 2012

42

Growth-Reductive Therapy in Children with Marfan Syndrome

L. Rozendaal, S. le Cessie, J.M. Wit, R.C.M. Hennekam, the Dutch Marfan Working Group

Journal:

The Journal of Pediatrics

Année:

2005

Langue:

english

Fichier:

PDF, 150 KB

english, 2005

43

Familial Syndromic Esophageal Atresia Maps to 2p23-p24

Jacopo Celli, Ellen van Beusekom, Raoul C.M. Hennekam, M. Esther Gallardo, Dominique F.C.M. Smeets, Santiago Rodríguez de Córdoba, Jeffrey W. Innis, Moshe Frydman, Rainer König, Helen Kingston, John T

Journal:

The American Journal of Human Genetics

Année:

2000

Langue:

english

Fichier:

PDF, 1.03 MB

english, 2000

44

Comparative Genomics and Gene Expression Analysis Identifies BBS9, a New Bardet-Biedl Syndrome Gene

Darryl Y. Nishimura, Ruth E. Swiderski, Charles C. Searby, Erik M. Berg, Amanda L. Ferguson, Raoul Hennekam, Saul Merin, Richard G. Weleber, Leslie G. Biesecker, Edwin M. Stone, Val C. Sheffield

Journal:

The American Journal of Human Genetics

Année:

2005

Langue:

english

Fichier:

PDF, 1.05 MB

english, 2005

45

Mutational spectrum of Smith-Lemli-Opitz syndrome

Waterham, Hans R., Hennekam, Raoul C.M.

Journal:

American Journal of Medical Genetics Part C: Seminars in Medical Genetics

Année:

2012

Langue:

english

Fichier:

PDF, 330 KB

english, 2012

46

Somatic mosaicism in a mother of two children with Pitt–Hopkins syndrome

CVM Steinbusch, KEP van Roozendaal, D Tserpelis, EEJ Smeets, TJ Kranenburg-de Koning, KH de Waal, C Zweier, A Rauch, RCM Hennekam, MJ Blok, CTRM Schrander-Stumpel

Journal:

Clinical Genetics

Année:

2012

Langue:

english

Fichier:

PDF, 610 KB

english, 2012

47

Intellectual Disability and Hemizygous GPD 2 Mutation

Barge-Schaapveld, Daniela Q.C.M., Ofman, Rob, Knegt, Alida C., Alders, Mariëlle, Höhne, Wolfgang, Kemp, Stephan, Hennekam, Raoul C.M.

Journal:

American Journal of Medical Genetics Part A

Année:

2013

Langue:

english

Fichier:

PDF, 1.44 MB

english, 2013

48

Very rare disorders -organisation of care

Raoul CM Hennekam

Journal:

Orphanet Journal of Rare Diseases

Année:

2010

Langue:

english

Fichier:

PDF, 175 KB

english, 2010

49

HNF1B Mutations Associate with Hypomagnesemia and Renal Magnesium Wasting

Adalat, S., Woolf, A. S., Johnstone, K. A., Wirsing, A., Harries, L. W., Long, D. A., Hennekam, R. C., Ledermann, S. E., Rees, L., van't Hoff, W., Marks, S. D., Trompeter, R. S., Tullus, K., Winyard,

Journal:

Journal of the American Society of Nephrology

Année:

2009

Langue:

english

Fichier:

PDF, 245 KB

english, 2009

50

Phenotype and genotype in Nicolaides-Baraitser syndrome

Sousa, Sérgio B., Hennekam, Raoul C.

Journal:

American Journal of Medical Genetics Part C: Seminars in Medical Genetics

Année:

2014

Langue:

english

Fichier:

PDF, 1.44 MB

english, 2014