Literature DB >> 5347076

The 13q-deletion syndrome.

P W Allderdice, J G Davis, O J Miller, H P Klinger, D Warburton, D A Miller, F H Allen, C A Abrams, E McGilvray.   

Abstract

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Year:  1969        PMID： 5347076      PMCID： PMC1706574     

Source DB:  PubMed          Journal:  Am J Hum Genet        ISSN： 0002-9297            Impact factor:   11.025


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  14 in total

1.  Multiple congenital abnormalities associated with ring chromosome.

Authors:  A D BAIN; I K GAULD
Journal:  Lancet       Date:  1963-08-10       Impact factor: 79.321

2.  [Partial deletion of the long arm of a group D (13-15) chromosome :Dq-].

Authors:  C Laurent; J B Cotton; A Nivelon; M T Freycon
Journal:  Ann Genet       Date:  1967-03

3.  [The Dr phenotype: a study of threee cases with a ring D chromosome].

Authors:  J Lejeune; J Lafourcade; R Berger; J Cruveiller; M O Rethoré; B Dutrillaux; D Abonyi; H Jérôme
Journal:  Ann Genet       Date:  1968-06

4.  Autosomal trisomy syndromes: a detailed study of 27 cases of Edwards' syndrome and 27 cases of Patau's syndrome.

Authors:  A I Taylor
Journal:  J Med Genet       Date:  1968-09       Impact factor: 6.318

5.  A human ring D chromosome associated with multiple congenital abnormalities.

Authors:  R L Teplitz; D Miller; K M Hansson; T S Rundall
Journal:  J Pediatr       Date:  1967-06       Impact factor: 4.406

6.  The upper limb-cardiovascular syndrome. An autosomal dominant genetic effect on embryogenesis.

Authors:  K B Lewis; R A Bruce; D Baum; A G Motulsky
Journal:  JAMA       Date:  1965-09-27       Impact factor: 56.272

7.  Absent thumbs with a ring D2 chromosome: a new deletion syndrome.

Authors:  R S Sparkes; R E Carrel; S W Wright
Journal:  Am J Hum Genet       Date:  1967-09       Impact factor: 11.025

8.  A ring D chromosome and anomalous inheritance of haptoglobin type.

Authors:  P S Gerald; S Warner; J D Singer; P A Corcoran; I Umansky
Journal:  J Pediatr       Date:  1967-02       Impact factor: 4.406

9.  The identification of the chromosomes of the D group (13-15) Denver: an autoradiographic and measurement study.

Authors:  F Giannelli; R M Howlett
Journal:  Cytogenetics       Date:  1966

10.  Ring D chromosome: a second case associated with anomalous haptoglobin inheritance.

Authors:  G E Bloom; P S Gerald; L E Reisman
Journal:  Science       Date:  1967-06-30       Impact factor: 47.728
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  46 in total

1.  Deletion of long arms of chromosome 13.

Authors:  M Kucerovă; Z Polívková; M Pokorná
Journal:  Humangenetik       Date:  1975

2.  2006 William Allan Award Address. Having it all.

Authors:  Dorothy Warburton
Journal:  Am J Hum Genet       Date:  2007-10       Impact factor: 11.025

3.  13q Deletion and central nervous system anomalies: further insights from karyotype-phenotype analyses of 14 patients.

Authors:  Lucia Ballarati; Elena Rossi; Maria Teresa Bonati; Stefania Gimelli; Paola Maraschio; Palma Finelli; Sabrina Giglio; Elisabetta Lapi; Maria Francesca Bedeschi; Silvana Guerneri; Giulia Arrigo; Maria Grazia Patricelli; Teresa Mattina; Oriana Guzzardi; Vanna Pecile; Adalgisa Police; Gioacchino Scarano; Lidia Larizza; Orsetta Zuffardi; Daniela Giardino
Journal:  J Med Genet       Date:  2007-01       Impact factor: 6.318

4.  D13 ring chromosome syndrome.

Authors:  A Mccandless; S Walker
Journal:  Arch Dis Child       Date:  1976-06       Impact factor: 3.791

5.  Deletion long arm 13.

Authors:  J Nielsen; A Homma; F Christiansen; K Rasmussen; P Saldaña-Garcia
Journal:  Hum Genet       Date:  1977-07-26       Impact factor: 4.132

6.  Ocular colobomata, cardiac defect, and other anomalies: a study of seven cases including two sibs.

Authors:  C K Ho; R L Kaufman; S M Podos
Journal:  J Med Genet       Date:  1975-09       Impact factor: 6.318

7.  DELETION MAPPING OF CRITICAL REGION FOR HYPOSPADIAS, PENOSCROTAL TRANSPOSITION AND IMPERFORATE ANUS ON HUMAN CHROMOSOME 13.

Authors:  Nilda M Garcia; Jocelyn Allgood; Lane J Santos; D Lonergan; J R Batanian; Mark Henkemeyer; Oliver Bartsch; Roger A Schultz; Andrew R Zinn; Linda A Baker
Journal:  J Pediatr Urol       Date:  2006-08       Impact factor: 1.830

8.  The aetiology of the cat eye syndrome reconsidered.

Authors:  G Guanti
Journal:  J Med Genet       Date:  1981-04       Impact factor: 6.318

9.  A 1.1-Mb segmental deletion on the X chromosome causes meiotic failure in male mice.

Authors:  Jian Zhou; John R McCarrey; P Jeremy Wang
Journal:  Biol Reprod       Date:  2013-06-27       Impact factor: 4.285

10.  Ring chromosome 14: a distinct clinical entity.

Authors:  R Schmidt; L Eviatar; H M Nitowsky; M Wong; S Miranda
Journal:  J Med Genet       Date:  1981-08       Impact factor: 6.318
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