Zobrazeno 1 - 8
of 8
pro vyhledávání: '"B G, ter Haar"'
Publikováno v:
Clinical Genetics. 25:470-472
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3498a15729102ad3c354dbfe89fcc6b1
https://doi.org/10.1111/j.1399-0004.1984.tb02019.x
https://doi.org/10.1111/j.1399-0004.1984.tb02019.x
Autor:
L J, van Dam, B G, ter Haar
Publikováno v:
Nederlands tijdschrift voor geneeskunde. 126(44)
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::ed3dee8fc30eb7676f592d08b9174ef3
https://pubmed.ncbi.nlm.nih.gov/7177209
https://pubmed.ncbi.nlm.nih.gov/7177209
Autor:
B C, Hamel, B G, ter Haar
Publikováno v:
Tijdschrift voor kindergeneeskunde. 52(4)
The McKusick-Dungy-Kaufman syndrome is characterized by hydrometrocolpos, polydactyly and congenital heart disease. Two of these 3 main symptoms should be present for the diagnosis. Associated anomalies are mainly found in the urogenital tract, the g
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::1f9c437d3a4397940c73d2369730c8b0
https://pubmed.ncbi.nlm.nih.gov/6495304
https://pubmed.ncbi.nlm.nih.gov/6495304
Autor:
M G, Smits, F J, Gabreëls, H O, Thijssen, R L, 't Lam, S L, Notermans, B G, ter Haar, J J, Prick
Publikováno v:
European neurology. 22(1)
3 siblings with symmetrical calcifications in the strio-pallido-dentate system are described. Parathyroid function was normal and there were no signs of central or peripheral myelinopathy. This is the 9th family reported with autosomal recessive idio
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::0e4659584effc5d6a798ffcbef4038cf
https://pubmed.ncbi.nlm.nih.gov/6840142
https://pubmed.ncbi.nlm.nih.gov/6840142
Autor:
B G, ter Haar
Publikováno v:
Tijdschrift voor ziekenverpleging. 38(25)
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::24c8f4a21e59c54079ce5b69f569e9e7
https://pubmed.ncbi.nlm.nih.gov/3854273
https://pubmed.ncbi.nlm.nih.gov/3854273
Publikováno v:
Helvetica paediatrica acta. 34(4)
A description is given of a 15-month-old girl with idiopathic arterial calcifications, detected during life time by X-ray. Radiological examination revealed calcifications in medium-sized arteries, histopathological examination showed distinct abnorm
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::ad1a29588a3d8210e2f2cf7ba4d27bf7
https://pubmed.ncbi.nlm.nih.gov/521302
https://pubmed.ncbi.nlm.nih.gov/521302
Autor:
B G, ter Haar, F E, van Dam
Publikováno v:
Nederlands tijdschrift voor geneeskunde. 116(49)
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::99e62ac86be35e21683c4e3f0b2af9ca
https://pubmed.ncbi.nlm.nih.gov/4641021
https://pubmed.ncbi.nlm.nih.gov/4641021
Publikováno v:
Clinical Genetics; Dec1987, Vol. 32 Issue 6, p398-402, 5p