DOUBLE TRISOMY IN SPONTANEOUS ABORTIONS—AN 11 YEAR REVIEW

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منابع مشابه

Double trisomy in spontaneous miscarriages: cytogenetic and molecular approach.

BACKGROUND Although single trisomy is the most common chromosomal abnormality observed within first trimester spontaneous abortions (SA) (>50%), double trisomy (DT) ranges from 0.21 to 2.8% in the literature. Since little is known about mechanisms underlying DT, we report the results of our experience with 517 SA, establishing parental origin and cell stage of non-disjunction when possible in D...

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Double Autosomal Trisomy and Mosaicism

There have been relatively few reports of individuals with double autosomal trisomy (Gagnon et al., 1961; Becker, Burke, and Albert, 1963; Hsu et al., 1965; Marks, Wiggins, and Spector, 1967). There have been rather more published accounts of individuals showing trisomy for one autosome and an additional chromosome in the sex chromosome complement as well. Of these, only those with the sex chro...

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Double autosomal trisomy (trisomy D+G) with mosaicism.

The patient, a male, the seventh child of a 37-year-old father and a 34-year-old Caucasian mother, was the product of a pregnancy complicated by massive polyhydramnios. The mother previously had had two miscarriages. During the present pregnancy she had not had any infections or X-irradiation. There was no family history of congenital malformations, mental retardation, leukaemia, autoimmune dis...

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An 11-year review of dermatomyositis in Asian patients.

INTRODUCTION Dermatomyositis (DM) is a multisystem inflammatory disease with a strong association with malignancy. We aimed to describe a series of Asian patients with DM and identify any significant clinical factors associated with malignancy. MATERIALS AND METHODS This was a retrospective review of a multi-racial cohort of 69 Asian patients diagnosed with DM over an 11-year period from 1996...

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New human double trisomy or tetrasomy.

Several studies have been reported on the cytogenetic analysis of spontaneous abortions (Aspillage et al., 1966; Boue, Boue, and Lazar, 1967; Carr, 1967; Clendenin and Benirschke, 1963; Hall and Kallen, 1964; Inhorn, Therman, and Patau, 1964; Rashad and Kerr, 1965; Singh, Rubinoff, and Carr, 1966; Szulman, 1965; Thiede and Salm, 1964; Thiede and Metcalfe, 1966; Waxman, Arakaki, and Smith, 1967)...

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ژورنال

عنوان ژورنال: Genetics in Medicine

سال: 2000

ISSN: 1098-3600,1530-0366

DOI: 10.1097/00125817-200001000-00142