Literature DB >> 885554

Deletion long arm 13.

J Nielsen, A Homma, F Christiansen, K Rasmussen, P Saldaña-Garcia.   

Abstract

Mesh:

Year:  1977        PMID: 885554     DOI: 10.1007/bf00393617

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


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  11 in total

1.  Deletion of long arms of chromosome 13.

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

2.  [Deletion of chromosome D (13q - ) in a child with psychomotor retardation].

Authors:  R Adámek; Z Kaspárková
Journal:  Cesk Pediatr       Date:  1974-01

3.  Retinoblastoma and D-chromosome deletions.

Authors:  M G Wilson; J W Towner; A Fujimoto
Journal:  Am J Hum Genet       Date:  1973-01       Impact factor: 11.025

4.  Retinoblastoma and D-chromosome deletions.

Authors:  E Orye; M J Delbeke; B Vandenabeele
Journal:  Lancet       Date:  1971-12-18       Impact factor: 79.321

5.  [A new syndrome caused by deletion of a part of a chromosome (13 q-). Case descriptions and compilation of symptoms (author's transl)].

Authors:  K P Grosse; G Schwanitz
Journal:  Klin Padiatr       Date:  1973-11       Impact factor: 1.349

6.  Retinoblastoma and long arm delection of chromosome 13. Attempts to define the deleted segment.

Authors:  E Orye; M J Delbeke; B Vandenabeele
Journal:  Clin Genet       Date:  1974       Impact factor: 4.438

7.  The syndrome associated with the partial D-monosomy. Case report and review.

Authors:  D J Orbeli; I W Lurie; J L Goroshenko
Journal:  Humangenetik       Date:  1971

8.  The 13q-deletion syndrome.

Authors:  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
Journal:  Am J Hum Genet       Date:  1969-09       Impact factor: 11.025

9.  Retinoblastoma and deletion D (14) syndrome.

Authors:  M G Wilson; J Melnyk; J W Towner
Journal:  J Med Genet       Date:  1969-09       Impact factor: 6.318

10.  [Dq-, multiple malformations and retinoblastoma].

Authors:  W Gey
Journal:  Humangenetik       Date:  1970
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  6 in total

1.  Deletion of band 13q21 is compatible with normal phenotype.

Authors:  J Couturier; N Morichon-Delvallez; B Dutrillaux
Journal:  Hum Genet       Date:  1985       Impact factor: 4.132

2.  Deficiency of coagulation factors VII and X associated with deletion of a chromosome 13 (q34). Evidence from two cases with 46,XY,t(13;Y)(q11;q34).

Authors:  R A Pfeiffer; R Ott; S Gilgenkrantz; P Alexandre
Journal:  Hum Genet       Date:  1982       Impact factor: 4.132

3.  Retinoblastoma: host resistance and 13q- chromosomal deletion.

Authors:  E Matsunaga
Journal:  Hum Genet       Date:  1980       Impact factor: 4.132

4.  Interstitial deletion 13q syndromes: a report on two unrelated patients.

Authors:  M Serena-Lungarotti; A Calabro; G Mariotti; P P Mastroiacovo; S Provenzano; B Dallapiccola
Journal:  Hum Genet       Date:  1979       Impact factor: 4.132

5.  Interstitial deletion of chromosome 13: prognosis and adult phenotype.

Authors:  J C Dean; S Simpson; D A Couzin; G S Stephen
Journal:  J Med Genet       Date:  1991-08       Impact factor: 6.318

6.  Interstitial del(13)(q21.3q31) associated with psychomotor retardation, eczema, and absent suck and swallowing reflex.

Authors:  P J Peet; R R Pereira; J O Van Hemel; A J Hoogeboom
Journal:  J Med Genet       Date:  1987-12       Impact factor: 6.318

  6 in total

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