Literature DB >> 5115887

A chromosome 13q+ in a patient with characteristics of the trisomy 13 syndrome.

H Hoehn, U Wolf, H Schumacher, H Wehinger.   

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Year:  1971        PMID： 5115887     DOI： 10.1007/bf00446411

Source DB:  PubMed          Journal:  Humangenetik        ISSN： 0018-7348


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  17 in total

1.  FOETAL HAEMOGLOBIN AND NEUTROPHIL ANOMALY IN THE D1-TRISOMY SYNDROME.

Authors:  D POWARS; R ROHDE; D GRAVES
Journal:  Lancet       Date:  1964-06-20       Impact factor: 79.321

2.  DEVELOPMENTAL HEMOGLOBIN ANOMALIES IN A CHROMOSOMAL TRIPLICATION: D1 TRISOMY SYNDROME.

Authors:  E R HUEHNS; F HECHT; J V KEIL; A G MOTULSKY
Journal:  Proc Natl Acad Sci U S A       Date:  1964-01       Impact factor: 11.205

3.  Estimation of small percentages of foetal haemoglobin.

Authors:  K BETKE; H R MARTI; I SCHLICHT
Journal:  Nature       Date:  1959-12-12       Impact factor: 49.962

Review 4.  Chromosomal variability in the D1 trisomy syndrome. Three cases and review of the literature.

Authors:  M B Taylor; R C Juberg; B Jones; W A Johnson
Journal:  Am J Dis Child       Date:  1970-10

5.  [On two familial cases of complex translocations].

Authors:  J Lejeune; R Burger
Journal:  Ann Genet       Date:  1965

6.  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

7.  Polydactyly and other minor stigmata associated with 46,XX-47,XX,D+ mosaicism.

Authors:  P Bowen; C S Lee; D R Shea; H B Armstrong
Journal:  Can Med Assoc J       Date:  1970-01-17       Impact factor: 8.262

8.  [Pairing behaviour of the sex chromosomes during male meiosis of Microtus agrestis].

Authors:  M T Zenzes; U Wolf
Journal:  Chromosoma       Date:  1971       Impact factor: 4.316

9.  Hematologic changes in the D1 trisomy syndrome.

Authors:  S Walzer; P S Gerald; G Breau; D O'Neill; L K Diamond
Journal:  Pediatrics       Date:  1966-09       Impact factor: 7.124

10.  Persistence of hemoglobin F in D/D translocation with trisomy 13-15 (D1).

Authors:  P H Pinkerton; M M Cohen
Journal:  JAMA       Date:  1967-05-15       Impact factor: 56.272
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  7 in total

1.  Further delineation of the clinical picture of trisomy for the distal segment of chromosome 13: report of three cases.

Authors:  A Schinzel; K Hayashi; W Schmid
Journal:  Hum Genet       Date:  1976-04-15       Impact factor: 4.132

2.  Partial trisomy 13: karyotype 46,XY,-6, plus t(13q,6q).

Authors:  J P Fryns; E Eggermont; H Verresen; H van den Berghe
Journal:  Humangenetik       Date:  1974-01-22

3.  Partial trisomy 13q21toqter de novo due to a recombinant chromosome rec(13)dup q.

Authors:  M Habedank
Journal:  Hum Genet       Date:  1979-11-01       Impact factor: 4.132

4.  Familial translocation with partial trisomy of 13 and 22: evidence that specific regions of chromosomes 13 and 22 are responsible for the phenotype of each trisomy.

Authors:  H J Kim; L Y Hsu; L C Goldsmith; L Strauss; K Hirschhorn
Journal:  J Med Genet       Date:  1977-04       Impact factor: 6.318

5.  The phenotype in partial 13q trisomies, apropos of a familial (13;15)(q22;q26) translocation.

Authors:  F Rivas; H Rivera; M L Plascencia; B Ibarra; J M Cantú
Journal:  Hum Genet       Date:  1984       Impact factor: 4.132

6.  Chromosome 7 short arm deletion and craniosynostosis. A 7p-syndrome.

Authors:  B T Gong; T H Norwood; H Hoehn; E McPherson; J G Hall; R Hickman
Journal:  Hum Genet       Date:  1976-12-29       Impact factor: 4.132

7.  The aetiology of the cat eye syndrome reconsidered.

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

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