Zobrazeno 1 - 10 of 117 pro vyhledávání: '"Margareta Mikkelsen And"'
2
CYTOGENETICAL FINDINGS IN CHILDREN BORN TO CARRIERS OF HEPATITIS-ASSOCIATED ANTIGEN
Autor: H. Olesen, Margareta Mikkelsen, Peter Skinhøj
Publikováno v: Acta Pathologica Microbiologica Scandinavica Section B Microbiology and Immunology. :207-218
The chromosomes of 50 newborn infants, born to healthy HAA carriers were examined. No chromosomal syndrome was observed. As compared with a control group, the number of amodal cells was found to be significantly higher and the relative proportion of
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::cedf7f8c2140d4121ae3a67d374e85a4
https://doi.org/10.1111/j.1699-0463.1973.tb00213.x
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4
Down syndrome: Cytogenetical epidemiology
Autor: Margareta Mikkelsen
Publikováno v: Hereditas. 86:45-49
The incidence of Down syndrome throughout a period of 12 years (1960 to 1971) was unchanged about 1.15 per 1000 births in parts of greater Copenhagen. 235 liveborn infants with Down syndrome were ascertained in this period in a population of 1.2 mill
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::cd91f079c7faeab52521ed877d464818
https://doi.org/10.1111/j.1601-5223.1977.tb01211.x
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5
Investigating the Impact of the Down Syndrome Related Common MTHFR 677C>T Polymorphism in the Danish Population
Autor: Haris Kokotas, Maria Grigoriadou, Margareta Mikkelsen, Aglaia Giannoulia-Karantana, Michael B. Petersen
Publikováno v: Disease Markers. 27:279-285
Chromosomal aneuploidy consists the leading cause of fetal death in our species. Around 50% of spontaneous abortions until 15 weeks of gestational age are chromosomally aneuploid, with trisomies accounting for 50% of the abnormal abortions. Trisomy 2
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::ac76e026069d0bb770ceea44a30473ef
https://doi.org/10.1155/2009/725614
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6
Turner syndrome with rare karyotypes
Autor: Hanne Poulsen, Margareta Mikkelsen, Krzysztof Boczkowsk
Publikováno v: Clinical Genetics. 13:409-414
Five cases of Turner syndrome with rare karyotypes are presented. The spectrum of chromosomal findings ranges from a female karyotype with a deletion of the short arm of one X chromosome, to a normal male karyotype. The following karyotypes were foun
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5a9415ff63a8df32893f5545921edf19
https://doi.org/10.1111/j.1399-0004.1978.tb04139.x
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9
MARTIN-BELL SYNDROME fra(X) (q28) IN A SRI LANKAN FAMILY
Autor: Margareta Mikkelsen And, Priyani E. Soysa, Hanne Poulsen, Mano Senanayahe
Publikováno v: Journal of Intellectual Disability Research. 26:251-257
The Martin-Bell syndrome was observed in a family with six mentally retarded males, born to three sisters, who were of more than average intelligence. The males showed large ears, macrotestes, they were delayed in their development and had speech ret
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::aa75ac088db60c0d3f52de5c507ebb22
https://doi.org/10.1111/j.1365-2788.1982.tb00152.x
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