Zobrazeno 1 - 9
of 9
pro vyhledávání: '"H. G. Van Spijker"'
Autor:
G. C. M. L. Christiaens, J. Bergsma, Marijke J. Korenromp, H. G. Van Spijker, H. R. Iedema-Kuiper
Publikováno v:
Journal of Psychosomatic Obstetrics & Gynecology. 13:93-105
This study describes reactions of couples to the termination of their pregnancies because of a fetal anomaly. Forty women and 31 men were interviewed twice after the termination, 6 weeks and 6 months, respectively. Factors found to be of influence on
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::43eb4ad8cb1c6a8865987813aefd9c41
https://doi.org/10.3109/01674829209016709
https://doi.org/10.3109/01674829209016709
Autor:
F J, Grosfeld, C J, Lips, H F, Ten Kroode, F A, Beemer, H G, Van Spijker, G J, Brouwers-Smalbraak
Publikováno v:
Oncology (Williston Park, N.Y.). 10(2)
Multiple endocrine neoplasia type 2 (MEN-2) is characterized by medullary thyroid carcinoma in combination with pheochromocytomas and, sometimes, parathyroid adenomas. Since 1993, the psychosocial implications of DNA analysis for MEN-2 have been stud
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::ca2742abf59f26fdbcbefc2e448e2c1d
https://pubmed.ncbi.nlm.nih.gov/8838257
https://pubmed.ncbi.nlm.nih.gov/8838257
Publikováno v:
Genetic counseling (Geneva, Switzerland). 7(1)
A patient is described with partial trisomy 9p and partial monosomy 8p due to a maternal translocation (t(8;9)(p23;p13)). The clinical phenotype is compatible with the partial trisomy 9p syndrome. This is a clinically recognizable syndrome with menta
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::7db7d974f68418bd66fb64f1adbf0e09
https://pubmed.ncbi.nlm.nih.gov/8652090
https://pubmed.ncbi.nlm.nih.gov/8652090
Autor:
H G, van Spijker, M, Korenromp, H R, Iedema-Kuiper, J, Bergsma, F A, Beemer, G C, Christiaens
Publikováno v:
Nederlands tijdschrift voor geneeskunde. 136(10)
By means of semistructured interviews with 40 women and their partners data were collected concerning on the one hand the care and support and on the other the grieving after termination of pregnancy performed because the child appeared to be genetic
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::64b4c4fb7ed910c16b9652807ac4823c
https://pubmed.ncbi.nlm.nih.gov/1589055
https://pubmed.ncbi.nlm.nih.gov/1589055
Autor:
H G, Van Spijker
Publikováno v:
Birth defects original article series. 28(1)
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::05bce88b2d43955fd57ac01d2f751472
https://pubmed.ncbi.nlm.nih.gov/1340232
https://pubmed.ncbi.nlm.nih.gov/1340232
Publikováno v:
American journal of medical genetics. Supplement, 6, 17-29
This study reports the physical and radiographic characteristics of 45 patients with Rubinstein-Taybi syndrome living in The Netherlands. All had broad halluces, but only 39 patients had broad thumbs. Microcephaly was present in 35% of patients. In a
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9282e461714c66e80b64d0fbe169900b
https://pubmed.ncbi.nlm.nih.gov/2118773
https://pubmed.ncbi.nlm.nih.gov/2118773
Publikováno v:
TBV – Tijdschrift voor Bedrijfs- en Verzekeringsgeneeskunde. 9:41-41
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::f9415d06a2cb84f0a6cac6d3705992c9
https://doi.org/10.1007/bf03073664
https://doi.org/10.1007/bf03073664
Autor:
H. G. Van Spijker, B. A. W. Rozendal
Publikováno v:
American Journal of Medical Genetics. 35:442-442
The papers (15) and posters (15) fell into 3 groups: A: psychosocial aspects of genetic counselling; B: psychosocial aspects of prenatal diagnosis; C: psychosocial aspects of specific diseases
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::cb0b7a60aeaf017fe7cc7bbc1762716e
https://doi.org/10.1002/ajmg.1320350324
https://doi.org/10.1002/ajmg.1320350324
Autor:
J. L. M. Strengers, Raoul C.M. Hennekam, E. J. P. Lommen, H. G. Van Spijker, T. M. G. Jansen-Kokx
Publikováno v:
European journal of pediatrics, 148(5), 439-441. Springer Verlag
The Rubinstein-Taybi syndrome is a condition characterized by mental retardation, typical facial changes and broad thumbs and big toes. The cause is unknown; almost all cases are sporadic. We describe a mother and son with Rubinstein-Taybi syndrome.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9f4835de25d65710c74f4b404f6b3c74
https://doi.org/10.1007/bf00595907
https://doi.org/10.1007/bf00595907