Literature DB >> 6650571

Inbreeding studies in Brasilian schoolchildren.

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Abstract

We present results of comparisons between consanguineous and control couples and their children in Southern Brasil. Multiple regression, t-test and chi 2 analyses were applied to the data. The following variables were investigated; Parents: structure of first cousin marriages, latitude and longitude of birthplaces, cohabitation time, rurality, marriage age, occupation, number of liveborn children, and frequency of twinning. Schoolchildren: clinical data as classified into 24 discontinuous traits, each one subdivided into two categories (number and severity), and seven continuous traits (weight, height, pulse rate, respiratory rate, systolic pressure, diastolic pressure, and temperature); nutrition indices and biotype; family names; intelligence tests and school performance; birth order, age, hair color, hair type, eye color, and skin color; twinning in the sibship, and infant mortality among sibs of the propositi. Our study showed a) nonrandomness of consanguineous marriages as detected on structural, racial, geographical, and temporal levels; b) a heavy mutational load of about 1.5 lethons acting on infant mortality; c) no inbreeding effect on morbidity in general (with a possible exception of "ear morbidity", including hearing deficit); d) a modest inbreeding depression on height (a decrease of 2 cm with an increase of 10% of inbreeding); 3) a suggestion of inbreeding depression on "intelligence".

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Year:  1983        PMID: 6650571     DOI: 10.1002/ajmg.1320160306

Source DB:  PubMed          Journal:  Am J Med Genet        ISSN: 0148-7299


  1 in total

1.  Evidence of inbreeding depression on human height.

Authors:  Ruth McQuillan; Niina Eklund; Nicola Pirastu; Maris Kuningas; Brian P McEvoy; Tõnu Esko; Tanguy Corre; Gail Davies; Marika Kaakinen; Leo-Pekka Lyytikäinen; Kati Kristiansson; Aki S Havulinna; Martin Gögele; Veronique Vitart; Albert Tenesa; Yurii Aulchenko; Caroline Hayward; Asa Johansson; Mladen Boban; Sheila Ulivi; Antonietta Robino; Vesna Boraska; Wilmar Igl; Sarah H Wild; Lina Zgaga; Najaf Amin; Evropi Theodoratou; Ozren Polašek; Giorgia Girotto; Lorna M Lopez; Cinzia Sala; Jari Lahti; Tiina Laatikainen; Inga Prokopenko; Mart Kals; Jorma Viikari; Jian Yang; Anneli Pouta; Karol Estrada; Albert Hofman; Nelson Freimer; Nicholas G Martin; Mika Kähönen; Lili Milani; Markku Heliövaara; Erkki Vartiainen; Katri Räikkönen; Corrado Masciullo; John M Starr; Andrew A Hicks; Laura Esposito; Ivana Kolčić; Susan M Farrington; Ben Oostra; Tatijana Zemunik; Harry Campbell; Mirna Kirin; Marina Pehlic; Flavio Faletra; David Porteous; Giorgio Pistis; Elisabeth Widén; Veikko Salomaa; Seppo Koskinen; Krista Fischer; Terho Lehtimäki; Andrew Heath; Mark I McCarthy; Fernando Rivadeneira; Grant W Montgomery; Henning Tiemeier; Anna-Liisa Hartikainen; Pamela A F Madden; Pio d'Adamo; Nicholas D Hastie; Ulf Gyllensten; Alan F Wright; Cornelia M van Duijn; Malcolm Dunlop; Igor Rudan; Paolo Gasparini; Peter P Pramstaller; Ian J Deary; Daniela Toniolo; Johan G Eriksson; Antti Jula; Olli T Raitakari; Andres Metspalu; Markus Perola; Marjo-Riitta Järvelin; André Uitterlinden; Peter M Visscher; James F Wilson
Journal:  PLoS Genet       Date:  2012-07-19       Impact factor: 5.917

  1 in total

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