Study on Fingerprint Images Using Delaunay Patterns to Identify Hereditary Relations Among Family Members of Three Generations

2014 ◽  
pp. 431-440
Author(s):  
C. Karthikeyini ◽  
V. Rajamani
Keyword(s):  
Family Members ◽  
Three Generations

Ann Charney Dobryd

2002 ◽  
pp. 509-512
Author(s):  
Anna Petrov Bumble
Keyword(s):  
Family Members ◽  
Point Of View ◽  
Jewish Family ◽  
Three Generations ◽  
The Holocaust ◽  
Inner World ◽  
Post War

This chapter considers Ann Charney’s Dobryd, a memoir with a profound treatment of the aftermath of the Holocaust. Reported from a child’s point of view, the narrative provides a glimpse into the deepest workings of Charney’s psyche from the age of 3 until the age of 10. Though not a feminist fable, Dobryd is a story in which all the protagonists — Charney, her mother, and her aunt — are women who struggle and succeed on their own during the war and in the chaos of post-war Poland. Named after a Polish town near Lviv, the memoir encompasses the lives of members of three generations of a Jewish family as they and their community suffer through the horrors of the Holocaust. The story follows family members over a period of about forty years, penetrating deep into their inner world.

scholarly journals Double Translocation: An Interesting Family History

2013 ◽  
Vol 16 (1) ◽  
pp. 77-80 ◽  
Author(s):  
A Uysal ◽  
A Uludağ ◽  
F Sılan ◽  
N Erçelen ◽  
C Zafer ◽  
...  
Keyword(s):  
Family History ◽  
Family Members ◽  
Chromosome Analysis ◽  
Chromosomal Anomaly ◽  
Balanced Translocation ◽  
Chromosome Anomalies ◽  
Three Generations ◽  
Interesting Family ◽  
Genetic Clinic ◽  
Balanced Translocations

Abstract Double balanced translocations are particularly rare and the risk of a fetus with an unbalanced chromosomal anomaly is greater than for single translocation carriers. In this present case, we describe an interesting family history which included three generations. A couple, married for 4 years, was referred to the genetic clinic due to infertility and family chromosome anomalies. A GTG-band chromosome analysis indicated that the male partner’s karyotype was 45,XY, t(3;18)(q11;ptel)t(13;14)(q10;q10). The same double balanced translocation was found in two others family members.

scholarly journals Hyperferritinaemia in the absence of iron overload

Gut ◽  
1997 ◽  
Vol 41 (3) ◽  
pp. 408-410 ◽  
Author(s):  
J D Arnold ◽  
A D Mumford ◽  
J O Lindsay ◽  
U Hegde ◽  
M Hagan ◽  
...  
Keyword(s):  
Iron Overload ◽  
Serum Ferritin ◽  
Serum Iron ◽  
Regulatory Protein ◽  
Transferrin Saturation ◽  
Family Members ◽  
Ferritin Concentration ◽  
Three Generations ◽  
Ferritin Synthesis ◽  
Ferritin Gene

Background—Serum ferritin is normally a marker of iron overload. Ferritin genes are sited at chromosomes 19 and 11. Regulation of ferritin synthesis involves an interaction between an iron regulatory protein (IRP) and part of the ferritin mRNA designated the iron regulatory element (IRE). A disorder of ferritin synthesis resulting in hyperferritinaemia in the absence of iron overload has been described recently.Patients and methods—Hyperferriti- naemia in the absence of iron overload was detected in a patient who was investigated for possible haemochromatosis. Serum iron, transferrin saturation, and ferritin concentration were studied in 11 members of this patient’s family from three generations. Eight members had DNA samples analysed by direct cycle sequencing of the 5′ untranslated region of the L ferritin gene.Results—Six of the family members studied had serum ferritin concentrations greater than 900 μg/l. However, serum iron and transferrin saturation were normal in these subjects who all had evidence of cataracts. Three affected family members who had genetic studies of the L ferritin gene on chromosome 19 had an A to G point mutation which was not found in unaffected members.Conclusions—There was complete concordance between a mutated IRE, cataracts, and hyperferritinaemia in three generations of this family. This family study confirms the finding that hereditary hyperferritinaemia in the absence of iron overload is an autosomal dominant inherited disorder.

scholarly journals Three Generations and Six Family Members with a t(13q15q) Chromosome

1973 ◽  
Vol 10 (1) ◽  
pp. 94-96 ◽  
Author(s):  
R. L. Neu ◽  
L. I. Gardner ◽  
M. L. Williams ◽  
M. J. Barlow
Keyword(s):  
Family Members ◽  
Three Generations

scholarly journals De Van Rijckevorsel bibliotheek in het Rotterdamsch Leeskabinet

2021 ◽  
Vol 28 (1) ◽  
pp. 223-258
Author(s):  
Roman Koot
Keyword(s):  
Nineteenth Century ◽  
Professional Practice ◽  
Family Members ◽  
Social Position ◽  
Content Type ◽  
Three Generations ◽  
The Family ◽  
Book Collections ◽  
Organically Grown

Abstract Since 1940, the Rotterdamsch Leeskabinet’s collection includes the library of the Rotterdam Van Rijckevorsel family. The library, with a size of 3,000 titles, was formed in the nineteenth century by three generations: the entrepreneurs Abram and Huibert and the scientist Elie van Rijckevorsel. The library is a unique example of a preserved library of a Rotterdam patrician family from the nineteenth century. This article examines the nature and composition of the library. It turns out not to be a collector’s library, but an organically grown, hybrid library, in which the professional practice, interests and social position of the family members are reflected. Functional books stood alongside rare antiquarian editions, and literature next to scientific works. Notable is the large number of books on geography, especially with regards to Dutch overseas trading areas. In order to determine whether this library is representative of book collections of Rotterdam’s elite families, more research is needed.

The Play of Identities in Cypriot-Australian Family Storytelling

2001 ◽  
Vol 11 (2) ◽  
pp. 335-362 ◽  
Author(s):  
Eleni Petraki
Keyword(s):  
Discourse Analysis ◽  
Critical Discourse Analysis ◽  
Family Members ◽  
Social Identities ◽  
Critical Discourse ◽  
Family Socialization ◽  
Mothers And Daughters ◽  
Three Generations ◽  
Family Storytelling ◽  
Australian Family

This article adopts a microanalytic approach to examine storytelling as a co-construction by family members in a Cypriot-Australian family. Previous studies on family storytelling have focused on the various roles of family members in storytelling with a means of studying family socialization (Miller et al., 1990; Ochs & Taylor, 1992; Blum-Kulka, 1997). These studies used critical discourse analysis, sociocultural theories, performance and pragmatic approaches to storytelling. This article offers a distinctive approach to family storytelling by examining the discourse and social identities that family members display during the storytelling. The data originate in a study that involves interviews with three generations of Greek-Australian and Cypriot-Australian women regarding their relationships with each other. In this paper we investigate the contributions of the father and the daughters in the course of the mother’s turn at storytelling. The first part of the analysis focuses on the husband’s discourse identities as a contributor, initiator and elicitor of his wife’s storytelling. During the storytelling we also observe the production and exchange of different social identities between the husband and the mother, such as the ‘unwilling suitor’, the ‘embarrassed schoolgirl’ or the ‘forceful but teasing husband’. The second part describes how the daughters take part in their mother’s storytelling, producing a variety of identities such as the ‘impatient mother’, the ‘complaining’, ‘happy’, or ‘good’ mothers and daughters. These investigations succinctly illustrate how narratives become a resource for members’ ‘display’ and ‘play’ of identities.

Micro-memories: Digital modes of communication across three generations

2020 ◽  
pp. 175069802095981
Author(s):  
Anette Grønning
Keyword(s):  
Family Relations ◽  
Family Members ◽  
Memory Studies ◽  
Empirical Results ◽  
Three Generations ◽  
Technical Developments

This article examines how digital modes of communication serve to facilitate family relations across three generations. Drawing on written interviews with two family chains, three categories of memory co-production are identified: co-construction, sedimentation and recreation. Applying theories of media generations and mediated memory studies, the analysis explores how these memories are shaped and unfolded. The empirical results demonstrate that all family members use digital modes of communication in the constructions of “micro-memories” of family relations, and that the three generations articulate these memories as vernacular archives of their family’s proximate past. The youngest family members represent a “here-and-now” presentism culture, while the middle and eldest family members represent a more classic “what has taken place” culture. In conclusion, it is argued that studies of mediated memories require additional empirical grounding which is contextualized, critical and mindful of the socio-technical developments and the affordances of the digital modes of communication.

“Everybody Takes Care of Everybody”: Care Circulation and Care Relations in Three-Generation Cohabitation

2019 ◽  
Vol 40 (17) ◽  
pp. 2628-2657 ◽  
Author(s):  
Adéla Souralová ◽  
Michaela Žáková
Keyword(s):  
Family Members ◽  
Demographic Changes ◽  
Three Generations ◽  
Adult Grandchildren ◽  
Intergenerational Caregiving ◽  
The Family ◽  
The Everyday ◽  
Depth Interviews

Demographic changes in Western societies have enabled long-term relationships between more generations and have significantly affected the structure and dynamic of family lives and contemporary families. This article presents a case study of three-generation cohabitation, the situation in which three generations live together in the same place at the same time. Drawing on in-depth interviews with three generations—grandparents, parents, and adult grandchildren—the article illuminates the characteristics of intergenerational caregiving and care-receiving. It uses the concept of care circulation to explore the everyday repeated exchanges of care among all family members and the caregiving constellations, arrangements, and distributions across the generations. We argue that the care is not unidimensional and unidirectional; rather, the care circulates among the family members cohabiting in three-generation households who are at the same time both caregivers and care-receivers.

scholarly journals A novel mutation in the FOXC2 gene: a heterozygous insertion of adenosine (c.867insA) in a family with lymphoedema of lower limbs without distichiasis

2017 ◽  
Vol 51 (3) ◽  
pp. 363-368 ◽  
Author(s):  
Tanja Planinsek Rucigaj ◽  
Matija Rijavec ◽  
Jovan Miljkovic ◽  
Julij Selb ◽  
Peter Korosec
Keyword(s):  
Clinical Presentation ◽  
Late Onset ◽  
Novel Mutation ◽  
Phenotypic Variability ◽  
Genetic Disorder ◽  
Family Members ◽  
The Body ◽  
Lower Limbs ◽  
Three Generations ◽  
Different Parts

Abstract Background Primary lymphoedema is a rare genetic disorder characterized by swelling of different parts of the body and highly heterogenic clinical presentation. Mutations in several causative genes characterize specific forms of the disease. FOXC2 mutations are associated with lymphoedema of lower extremities, usually distichiasis and late onset. Patients and methods Subjects from three generations of a family with lymphoedema of lower limbs without distichiasis were searched for mutations in the FOXC2 gene. Results All affected family members with lymphoedema of lower limbs without distichiasis, and still asymptomatic six years old girl from the same family, carried the same previously unreported insertion of adenosine (c.867insA) in FOXC2. Conclusions Identification of a novel mutation in the FOXC2 gene in affected family members of three generations with lymphoedema of lower limbs without distichiasis, highlights the high phenotypic variability caused by FOXC2 mutations.

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