Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Filters

C Schaap

Showing results (1-10 of 44) with videos related to

Pageof 5
Sort By:
The British Journal of Psychiatry : the Journal of Mental Science|September 1, 1985
The Maudsley Marital Questionnaire (MMQ): an extension of its construct validityW A Arrindell, C Schaap
American Journal of Medical Genetics|July 15, 1994
Severe progressive neurological disorder associated with hydrocephalus in a man with fragile X syndromeC Schaap, J P Fryns
Clinical Dysmorphology|October 1, 1995
Three mildly retarded siblings with congenital cataracts, sensorineural deafness, hypogonadism, hypertrichosis and short stature: a new syndrome?C Schaap, D Taylor, M Baraitser
The British Journal of Clinical Psychology|May 1, 1989
The significance of the patient-therapist relationship in the treatment of obsessive-compulsive neurosisC A Hoogduin, E de Haan, C Schaap
Nederlands Tijdschrift Voor Geneeskunde|August 12, 1989
[Dosage aerosols; problems with the inhalation technic]A A Baas, P J Hekking, C Schaap
The Journal of Nervous and Mental Disease|December 1, 1993
The heterogeneity of schizophrenic information processing and negative versus positive symptomsM J Verbraak, C A Hoogduin, C Schaap
Social Science & Medicine (1982)|January 1, 1991
Verbal analysis of doctor-patient communicationL Meeuwesen, C Schaap, C van der Staak
Genetic Counseling (Geneva, Switzerland)|January 1, 1992
Opitz-C syndrome: on the nosology of mental retardation and trigonocephalyC Schaap, C T Schrander-Stumpel, J P Fryns
Behaviour Research and Therapy|January 1, 1993
Do patients suffering from obsessions alone differ from other obsessive-compulsives?W Arts, K Hoogduin, C Schaap, et al.
Nederlands Tijdschrift Voor Geneeskunde|January 2, 1993
[A Dutch family with hereditary joint symptoms; multiple epiphyseal dysplasia]J B van Mourik, C Schaap, A J Nollen
Pageof 5

Showing results (1-10 of 44) with videos related to

Sort By:
Pageof 5
The British Journal of Psychiatry : the Journal of Mental Science|September 1, 1985
The Maudsley Marital Questionnaire (MMQ): an extension of its construct validityW A Arrindell, C Schaap
American Journal of Medical Genetics|July 15, 1994
Severe progressive neurological disorder associated with hydrocephalus in a man with fragile X syndromeC Schaap, J P Fryns
Clinical Dysmorphology|October 1, 1995
Three mildly retarded siblings with congenital cataracts, sensorineural deafness, hypogonadism, hypertrichosis and short stature: a new syndrome?C Schaap, D Taylor, M Baraitser
The British Journal of Clinical Psychology|May 1, 1989
The significance of the patient-therapist relationship in the treatment of obsessive-compulsive neurosisC A Hoogduin, E de Haan, C Schaap
Nederlands Tijdschrift Voor Geneeskunde|August 12, 1989
[Dosage aerosols; problems with the inhalation technic]A A Baas, P J Hekking, C Schaap
The Journal of Nervous and Mental Disease|December 1, 1993
The heterogeneity of schizophrenic information processing and negative versus positive symptomsM J Verbraak, C A Hoogduin, C Schaap
Social Science & Medicine (1982)|January 1, 1991
Verbal analysis of doctor-patient communicationL Meeuwesen, C Schaap, C van der Staak
Genetic Counseling (Geneva, Switzerland)|January 1, 1992
Opitz-C syndrome: on the nosology of mental retardation and trigonocephalyC Schaap, C T Schrander-Stumpel, J P Fryns
Behaviour Research and Therapy|January 1, 1993
Do patients suffering from obsessions alone differ from other obsessive-compulsives?W Arts, K Hoogduin, C Schaap, et al.
Nederlands Tijdschrift Voor Geneeskunde|January 2, 1993
[A Dutch family with hereditary joint symptoms; multiple epiphyseal dysplasia]J B van Mourik, C Schaap, A J Nollen
Pageof 5