Literature DB >> 6132873

Gene mapping and serendipity. The locus for torticollis, keloids, cryptorchidism and renal dysplasia (31430, Mckusick) is at Xq28, distal to the G6PD locus.

O Zuffardi, M Fraccaro.   

Abstract

The syndrome of torticollis, keloids, cryptorchidism and renal dysplasia was described by Goeminne (1968) in a large family, and listed as X-linked incomplete dominant by McKusick (1978; No. 31430). We mapped the locus on the long arm of the X chromosome at band q28 and distal to the G6PD locus. This was achieved by the chance discovery in the literature that two females, each with a balanced X/autosome translocation involving Xq28, had partial manifestation of the syndrome as was the case with the females in the larger family of Goeminne (1968).

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Year:  1982        PMID: 6132873     DOI: 10.1007/bf00333537

Source DB:  PubMed          Journal:  Hum Genet        ISSN: 0340-6717            Impact factor:   4.132


  11 in total

1.  A new probably X-linked inherited syndrome: congenital muscular torticollis, multiple keloids cryptorchidism and renal dysplasia.

Authors:  L Goeminne
Journal:  Acta Genet Med Gemellol (Roma)       Date:  1968-07

2.  Two human X-autosome translocations identified by autoradiography and fluorescence.

Authors:  M M Cohen; C C Lin; V Sybert; E J Orecchio
Journal:  Am J Hum Genet       Date:  1972-09       Impact factor: 11.025

3.  Chromosomal abnormalities in mendelian disorders.

Authors: 
Journal:  Lancet       Date:  1982-08-07       Impact factor: 79.321

4.  Different patterns of X chromosome inactivity in lymphocytes and fibroblasts of a human balanced X;autosome translocation.

Authors:  B Hellkuhl; A de la Chapelle; K H Grzeschik
Journal:  Hum Genet       Date:  1982       Impact factor: 4.132

5.  Possible inactivation of part of chromosome 13 due to 13qXp translocation associated with retinoblastoma.

Authors:  Y Ejima; M S Sasaki; A Kaneko; H Tanooka; Y Hara; T Hida; Y Kinoshita
Journal:  Clin Genet       Date:  1982-06       Impact factor: 4.438

6.  Duchenne muscular dystrophy (DMD) in a female with an X/autosome translocation: further evidence that the DMD locus is at Xp21.

Authors:  P A Jacobs; P A Hunt; M Mayer; R D Bart
Journal:  Am J Hum Genet       Date:  1981-07       Impact factor: 11.025

7.  H-Y antigen expression in patients with X-autosomal translocations and gonadal dysgenesis.

Authors:  F P Haseltine; V A Lynch; D L Van Dyke; W R Breg; U Francke
Journal:  Am J Med Genet       Date:  1982-10

8.  Agenesis of corpus callosum, ocular, and skeletal anomalies (X-linked dominant Aicardi's syndrome) in a girl with balanced X/3 translocation.

Authors:  H H Ropers; O Zuffardi; E Bianchi; L Tiepolo
Journal:  Hum Genet       Date:  1982       Impact factor: 4.132

9.  Localization of loci for hypoxanthine phosphoribosyltransferase and glucose-6-phosphate dehydrogenase and biochemical evidence of nonrandom X chromosome expression from studies of a human X-autosome translocation.

Authors:  G S Pai; J A Sprenkle; T T Do; C E Mareni; B R Migeon
Journal:  Proc Natl Acad Sci U S A       Date:  1980-05       Impact factor: 11.205

10.  Bilateral retinoblastoma with a 13qXp translocation.

Authors:  T Hida; Y Kinoshita; R Matsumoto; N Suzuki; H Tanaka
Journal:  J Pediatr Ophthalmol Strabismus       Date:  1980 May-Jun       Impact factor: 1.402

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  10 in total

1.  A dominantly inherited syndrome (microcephaly, short stature, peculiar facies, mental retardation) associated with two balanced rearrangements involving chromosomes 2;7 and 5;20.

Authors:  R Vivarelli; O Zuffardi; P Maraschio; C Anichini; R Scarinci
Journal:  Hum Genet       Date:  1988-08       Impact factor: 4.132

Review 2.  Mendelian cytogenetics. Chromosome rearrangements associated with mendelian disorders.

Authors:  N Tommerup
Journal:  J Med Genet       Date:  1993-09       Impact factor: 6.318

Review 3.  On the genetic length of the short arm of the human X chromosome.

Authors:  H H Ropers; P Wieacker; T F Wienker; K Davies; R Williamson
Journal:  Hum Genet       Date:  1983       Impact factor: 4.132

4.  Median cleft of upper lip and pedunculated skin masses associated with de novo reciprocal translocation 46,X,t(X;16)(q28;q11.2).

Authors:  M Masuno; K Imaizumi; Y Fukushima; Y Tanaka; T Ishii; M Nakamura; Y Kuroki
Journal:  J Med Genet       Date:  1997-11       Impact factor: 6.318

5.  Deficiency, transposition, and duplication of one 15q region may be alternatively associated with Prader-Willi (or a similar) syndrome. Analysis of seven cases after varying ascertainment.

Authors:  M Fraccaro; O Zuffardi; E Bühler; A Schinzel; G Simoni; R Witkowski; E Bonifaci; D Caufin; G Cignacco; N Delendi
Journal:  Hum Genet       Date:  1983       Impact factor: 4.132

6.  Global survey of protein expression during gonadal sex determination in mice.

Authors:  Katherine Ewen; Mark Baker; Dagmar Wilhelm; R John Aitken; Peter Koopman
Journal:  Mol Cell Proteomics       Date:  2009-07-17       Impact factor: 5.911

7.  Molecular cloning and characterization of a novel mouse actin-binding protein Zfp185.

Authors:  Na Wang; Quanhui Zheng; Jin-San Zhang; Yong Zhao
Journal:  J Mol Histol       Date:  2008-02-01       Impact factor: 2.611

8.  Mutational analysis of the human FATE gene in 144 infertile men.

Authors:  Christian Olesen; Joachim Silber; Hans Eiberg; Erik Ernst; Karsten Petersen; Svend Lindenberg; Niels Tommerup
Journal:  Hum Genet       Date:  2003-06-14       Impact factor: 4.132

9.  Molecular Mechanisms of Syndromic Cryptorchidism: Data Synthesis of 50 Studies and Visualization of Gene-Disease Network.

Authors:  Kristian Urh; Živa Kolenc; Maj Hrovat; Luka Svet; Peter Dovč; Tanja Kunej
Journal:  Front Endocrinol (Lausanne)       Date:  2018-07-26       Impact factor: 5.555

10.  Description of familial keloids in five pedigrees: evidence for autosomal dominant inheritance and phenotypic heterogeneity.

Authors:  Jason A Clark; Maria L Turner; Lillian Howard; Horia Stanescu; Robert Kleta; Jeffrey B Kopp
Journal:  BMC Dermatol       Date:  2009-07-28
  10 in total

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