HL-A Antigens and Heteromorphic Fluorescence Characters of Chromosomes in Prenatal Paternity Investigation

Jonasson, Jon; Lindsten, J.; Lundborg, R; Kissmeyer-Nielsen, F; Lu, Lamm; Gb, Petersen; Aj, Therkelsen

doi:10.1038/236312a0

Cited by 22 publications

(11 citation statements)

References 3 publications

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“…6 One of the cases in this group was the missed abortion in which only maternal cells grew (see text). ' In three further cases there was a child with Down's syndrome and in one a malformed child among other close relatives.…”

Section: Contamination With Maternal Cellsmentioning

confidence: 97%

Prenatal Cytogenetic Diagnosis

Lindsten

Therkelsen

Friedrich

et al. 1974

Intl J Gynecology & Obste

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Section: Contamination With Maternal Cellsmentioning

confidence: 97%

Prenatal Cytogenetic Diagnosis

Lindsten

Therkelsen

Friedrich

et al. 1974

Intl J Gynecology & Obste

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“…It has been shown that this variation is largely due to differences in length of the brightly fluorescing portion (Bobrow et al, 1971), which may be entirely lacking in some normal males (Borgaonkar and Hollander, 1971). The Y polymorphism has been shown to have a practical application in a case of paternity, disputed prenatally, that was resolved by Jonasson et al (1972a). They showed similarity in the size of the brightly fluorescent region of the Y chromosome in one of the men involved and the amniotic cells of the fetus.…”

Section: Polymorphismsmentioning

confidence: 99%

Chromosome studies in man: past achievements and recent advances.

Lawler¹,

Reeves²

1976

J Clin Pathol

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“…Dementsprechend sind diese Merkrnale der Chromosomen schon in einzelnen Fallen zur Klarung yon genetischen Verhaltnissen verwendet worden (Jonasson et al, 1972). Es war auch rnSg]ich, die urspriingliche Annahme, dal~ das iiberzahlige Chromosom Nr.…”

Section: Ergebnisseunclassified

Der Polymorphismus des menschlichen Chromosomensatzes —eine Möglichkeit für den Vaterschaftsnachweis

Schnedl¹

1974

Z Rechtsmed

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Summary. The recent quinacrine fluorescence analysis and the Giemsa banding methods allow identification of all human chromosomes. When human chromosomes were studied by using these methods, at least 10 of the 23 chromosome pairs showed polymorphism occuring at a relatively high frequency. Since these features are carried by the chromosomes they are necessarily inherited. The frequency of these variabilities is high enough to allow exclusion of paternity in affiliation cases at a likelihood of at least 70~o.Zusammenfassung. In den letzten Jahren ist durch die Quinacrine-Fluorescenzmethode und die Giemsa-B~nderverfahren eine Identifizierung s/~mtlicher Chromosomen des Menschen mSglich geworden. Dabei hat sich auch gezeigt, dab mindestens l0 von den 23 Chromosomenpaaren zum Tell sehr h~ufige Variabilit/~ten aufweisen, die, da sie in die Erbtr/~ger integriert sind, notwendigerweise vererbt werden. Die Frequenzen dieser Polymorphismen wfrden, auch bei Verwendung nurder am leichtesten zu erkennenden Strukturverschiedenheiten, beim Vaterschaftsnachweis eine AusschluBwahrscheinlichkeit yon ca. 70~o ergeben.

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HL-A Antigens and Heteromorphic Fluorescence Characters of Chromosomes in Prenatal Paternity Investigation

Cited by 22 publications

References 3 publications

Prenatal Cytogenetic Diagnosis

Prenatal Cytogenetic Diagnosis

Chromosome studies in man: past achievements and recent advances.

Der Polymorphismus des menschlichen Chromosomensatzes —eine Möglichkeit für den Vaterschaftsnachweis

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