Literature DB >> 5031080

Theory of X-linkage of major intellectual traits.

R Lehrke.   

Abstract

Mesh：

Year:  1972        PMID： 5031080

Source DB:  PubMed          Journal:  Am J Ment Defic        ISSN： 0002-9351


× No keyword cloud information.
  25 in total

1.  X linked severe mental retardation, craniofacial dysmorphology, epilepsy, ophthalmoplegia, and cerebellar atrophy in a large South African kindred is localised to Xq24-q27.

Authors:  A L Christianson; R E Stevenson; C H van der Meyden; J Pelser; F W Theron; P L van Rensburg; M Chandler; C E Schwartz
Journal:  J Med Genet       Date:  1999-10       Impact factor: 6.318

2.  A new X linked recessive syndrome of mental retardation and mild dysmorphism maps to Xq28.

Authors:  G S Pai; B Hane; M Joseph; R Nelson; L S Hammond; J F Arena; H A Lubs; R E Stevenson; C E Schwartz
Journal:  J Med Genet       Date:  1997-07       Impact factor: 6.318

3.  Non-specific X linked mental retardation with aphasia exhibiting genetic linkage to chromosomal region Xp11.

Authors:  G N Wilson; C S Richards; K Katz; G S Brookshire
Journal:  J Med Genet       Date:  1992-09       Impact factor: 6.318

Review 4.  X linked mental retardation.

Authors:  I A Glass
Journal:  J Med Genet       Date:  1991-06       Impact factor: 6.318

Review 5.  Non-specific X linked mental retardation.

Authors:  B Kerr; G Turner; J Mulley; A Gedeon; M Partington
Journal:  J Med Genet       Date:  1991-06       Impact factor: 6.318

6.  Genes for intelligence on the X chromosome.

Authors:  G Turner; M W Partington
Journal:  J Med Genet       Date:  1991-06       Impact factor: 6.318

7.  Finding genes on the X chromosome by which homo may have become sapiens.

Authors:  G Turner
Journal:  Am J Hum Genet       Date:  1996-06       Impact factor: 11.025

8.  X-linked mental retardation.

Authors:  G Turner; B Turner
Journal:  J Med Genet       Date:  1974-06       Impact factor: 6.318

Review 9.  Severe mental handicap: pathogenesis, treatment, and prevention.

Authors:  M D Crawfurd
Journal:  Br Med J (Clin Res Ed)       Date:  1982-09-18

10.  Complex segmental duplications mediate a recurrent dup(X)(p11.22-p11.23) associated with mental retardation, speech delay, and EEG anomalies in males and females.

Authors:  Roberto Giorda; M Clara Bonaglia; Silvana Beri; Marco Fichera; Francesca Novara; Pamela Magini; Jill Urquhart; Freddie H Sharkey; Claudio Zucca; Rita Grasso; Susan Marelli; Lucia Castiglia; Daniela Di Benedetto; Sebastiano A Musumeci; Girolamo A Vitello; Pinella Failla; Santina Reitano; Emanuela Avola; Francesca Bisulli; Paolo Tinuper; Massimo Mastrangelo; Isabella Fiocchi; Luigina Spaccini; Claudia Torniero; Elena Fontana; Sally Ann Lynch; Jill Clayton-Smith; Graeme Black; Philippe Jonveaux; Bruno Leheup; Marco Seri; Corrado Romano; Bernardo dalla Bernardina; Orsetta Zuffardi
Journal:  Am J Hum Genet       Date:  2009-08-27       Impact factor: 11.025
View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.