Literature DB >> 4834252

A new syndrome resulting from partial trisomy for the distal third of the long arm of chromosome 10.

J J Yunis, O Sanchez.   

Abstract

Mesh：

Year:  1974        PMID： 4834252     DOI： 10.1016/s0022-3476(74)80683-9

Source DB:  PubMed          Journal:  J Pediatr        ISSN： 0022-3476            Impact factor:   4.406


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  17 in total

1.  Partial trisomy of chromosome 10 inherited from a carrier father.

Authors:  S Suresh; I Suresh; P Lakshminarayana; G Jabeen; K Rajesh
Journal:  Indian J Pediatr       Date:  1995 Sep-Oct       Impact factor: 1.967

2.  Distal 10q trisomy syndrome with unusual cardiac and pulmonary abnormalities.

Authors:  J Davies; A Jaffé; A Bush
Journal:  J Med Genet       Date:  1998-01       Impact factor: 6.318

3.  Severe mental retardation in six generations of a large South African family carrying a translocation t(6;10)(q27;q25.2).

Authors:  J Brusnický; K M van Heerden; G de Jong; A S Cronjé; A E Retief
Journal:  J Med Genet       Date:  1986-10       Impact factor: 6.318

4.  A pericentric inversion of a chromosome 4 with a t(4q+10p-) and a familial t(DqDq) in a mentally retarded girl.

Authors:  S W Soukup; W Yarema; M Robinow
Journal:  Humangenetik       Date:  1974

5.  G-banding and chromosome structure.

Authors:  J J Yunis; O Sanchez
Journal:  Chromosoma       Date:  1973       Impact factor: 4.316

6.  Partial trisomy 11 in a child resulting from a complex maternal rearrangement of chromosomes 11, 12 and 13.

Authors:  O Sanchez; J J Yunis; J I Escobar
Journal:  Humangenetik       Date:  1974-04-24

7.  Partial trisomy 10q: a recognizable syndrome.

Authors:  J M Klep-de Pater; J B Bijlsma; H F de France; N J Leschot; M Duijndam-van den Berge; J O van Hemel
Journal:  Hum Genet       Date:  1979-01-19       Impact factor: 4.132

8.  Balanced translocation (10;13) in a father, ascertained through the study of meiosis in semen, and partial trisomy 10q in his son. Characterization of the region responsible for the partial trisomy 10q syndrome.

Authors:  R Miró; C Templado; M Ponsá; J Serradell; S Marina; J Egozcue
Journal:  Hum Genet       Date:  1980-02       Impact factor: 4.132

Review 9.  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

10.  Further delineation of the partial proximal trisomy 10q syndrome.

Authors:  C M Aalfs; J M Hoovers; M A Nieste-Otter; M M Mannens; R C Hennekam; N J Leschot
Journal:  J Med Genet       Date:  1995-12       Impact factor: 6.318
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