Literature DB >> 4124199

(6;15) Translocation with loss of chromosome material in the patient and various chromosome aberrations in family members.

M Mikkelsen, H Dyggve.   

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Year:  1973        PMID： 4124199     DOI： 10.1007/bf00290596

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


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  6 in total

1.  [PARTIAL DELETION OF THE SHORT ARM OF CHROMOSOME 5. INDIVIDUALIZATION OF A NEW MORBID STATE].

Authors:  J LEJEUNE; J LAFOURCADE; J DE GROUCHY; R BERGER; M GAUTIER; C SALMON; R TURPIN
Journal:  Sem Hop       Date:  1964-04-14

2.  Localization of heterochromatin in human chromosomes.

Authors:  F E Arrighi; T C Hsu
Journal:  Cytogenetics       Date:  1971

3.  The 4p- syndrome. A clinically recognizable chromosomal deletion syndrome.

Authors:  R D Guthrie; J M Aase; A C Asper; D W Smith
Journal:  Am J Dis Child       Date:  1971-11

4.  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

5.  Differential binding of alkylating fluorochromes in human chromosomes.

Authors:  T Caspersson; L Zech; C Johansson
Journal:  Exp Cell Res       Date:  1970-06       Impact factor: 3.905

6.  [Deficiency on the short arms of a chromosome No. 4].

Authors:  U Wolf; H Reinwein; R Porsch; R Schröter; H Baitsch
Journal:  Humangenetik       Date:  1965
  6 in total
  10 in total

1.  Karyotype 45,XX,-21/46,XX,21q-in an infant with symptoms of G-deletion syndrome I.

Authors:  M Mikkelsen; S Vestermark
Journal:  J Med Genet       Date:  1974-12       Impact factor: 6.318

2.  Necrotizing Enterocolitis in Two Siblings and an Unrelated Infant with Overlapping Chromosome 6q25 Deletions.

Authors:  Hannah C D Esdal; Muhammad B Ghbeis; Daniel A Saltzman; Donavon Hess; Janet R Hume; Robyn C Reed; Susan A Berry; Eric Hoggard; Betsy Hirsch; Linda B Baughn; Lisa A Schimmenti
Journal:  Mol Syndromol       Date:  2018-04-28

Review 3.  Chromosome 15 anomalies and the Prader-Willi syndrome: cytogenetic analysis.

Authors:  M G Mattei; N Souiah; J F Mattei
Journal:  Hum Genet       Date:  1984       Impact factor: 4.132

4.  Interstitial deletion of chromosome 6q: precise definition of the breakpoints by microdissection, DNA amplification, and reverse painting.

Authors:  N Rubtsov; G Senger; H Kuzcera; A Neumann; C Kelbova; K Junker; V Beensen; U Claussen
Journal:  Hum Genet       Date:  1996-06       Impact factor: 4.132

Review 5.  [Cat-eye syndrome. Clinical and cytogenetical differentialdiagnosis (author's transl)].

Authors:  J Kunze; M Tolksdorf; H R Wiedemann
Journal:  Humangenetik       Date:  1975

6.  Translocation between chromosomes 6 and 15 (45,XX,t(6;15)(q25;q11.2)) with further evidence for lack of imprinting of the insulin-like growth factor II/mannose-6-phosphate receptor in humans.

Authors:  E Treacy; C Polychronakos; M Vekemans; P Eydoux; S Blaichman; H Scarpelli; M Ross; Y Xu; V M Der Kaloustian
Journal:  J Med Genet       Date:  1996-01       Impact factor: 6.318

7.  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

8.  Unbalanced reciprocal translocations in cases of Prader-Willi syndrome.

Authors:  D P Duckett; S H Roberts; P Davies
Journal:  Hum Genet       Date:  1984       Impact factor: 4.132

9.  Prader-Willi syndrome: current understanding of cause and diagnosis.

Authors:  M G Butler
Journal:  Am J Med Genet       Date:  1990-03

Review 10.  Adjacent 2 meiotic disjunction. report of a case resulting from a familial 13q;15q balanced reciprocal translocation and review of the literature.

Authors:  D P Duckett; S H Roberts
Journal:  Hum Genet       Date:  1981       Impact factor: 4.132
  10 in total

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