Results 251 to 260 of about 97,595 (299)
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Trisomy 9q?. A variant of the 9p trisomy syndrome
Human Genetics, 1975A low-birth-weight near-term male infant was found to have a non-familial 47,XY chromosome complement with an extra medium-sized metacentric chromosome slightly larger than a number 16. By Giemsa-trypsin (G-banding) this extra chromosome was determined to be a number 9 with deletion of approximately half of the long arm at region q 22.
W R, Centerwall, C A, Mayeski, C C, Cha
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2004
Die Trisomie 18 (Edwards-Syndrom, Erstbeschreibung 1960) ist nach dem Down-Syndrom die zweithaufigst vorkommende numerische Aneuploidie. Dabei ist das Chromosom 18 in jeder Korperzelle des Kindes dreifach vorhanden.
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Die Trisomie 18 (Edwards-Syndrom, Erstbeschreibung 1960) ist nach dem Down-Syndrom die zweithaufigst vorkommende numerische Aneuploidie. Dabei ist das Chromosom 18 in jeder Korperzelle des Kindes dreifach vorhanden.
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Trisomy 16 and trisomy 16 mosaicism: A review
American Journal of Medical Genetics, 1998A review of all prenatal and postnatal diagnoses of trisomy 16 and trisomy 16 mosaicism was carried out in the context of the current understanding of confined placental mosaicism and uniparental disomy (UPD). The prenatal detection of trisomy 16 cells is associated with a high probability of fetal death, preterm delivery, intrauterine growth ...
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2003
De bekendste numerieke chromosoomafwijking is trisomie 21, ofwel Downsyndroom (zie vorige hoofdstuk). Kinderen met trisomie 13 (vroeger ook wel syndroom van Patau genoemd) of trisomie 18 (het vroegere syndroom van Edwards) zijn veel minder bekend omdat ze in de regel niet lang overleven en maar kort thuis kunnen zijn.
C. T. R. M. Schrander-Stumpel +1 more
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De bekendste numerieke chromosoomafwijking is trisomie 21, ofwel Downsyndroom (zie vorige hoofdstuk). Kinderen met trisomie 13 (vroeger ook wel syndroom van Patau genoemd) of trisomie 18 (het vroegere syndroom van Edwards) zijn veel minder bekend omdat ze in de regel niet lang overleven en maar kort thuis kunnen zijn.
C. T. R. M. Schrander-Stumpel +1 more
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[Genetics of partial trisomies. Trisomy 4p].
Genetika, 1989Phenotypic picture for two cytogenetically different variants of trisomy 4p (with and without involvement of the proximal part of 4q) obtained on the data of Minsk Teratologic Center and on the review of 64 cases from the world literature is presented. Mathematical evaluation of intrapair, within- and interfamilial similarity, depending on a duplicated
P V, Rumiantseva +3 more
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