与多种先天性畸形相关的环状染色体D（13） - Suppr

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超能文献

Ring chromosome D (13) associated with multiple congenital malformations.

作者信息

Niebuhr E, Ottosen J

出版信息

Ann Genet. 1973 Sep;16(3):157-66.

PMID:4543204

Abstract

摘要

相似文献

Ring chromosome D (13) associated with multiple congenital malformations.

Ann Genet. 1973 Sep;16(3):157-66.

Ring 13 chromosome in an infant with congenital malformations (author's transl).

Jinrui Idengaku Zasshi. 1974 Jun;19(1):77-8.

[Ring chromosome 13 and multiple malformations (author's transl)].

An Esp Pediatr. 1981 Nov;15(5):469-73.

[Comparative pathology of trisomies D and E].

Union Med Can. 1968 Jul;97(7):907-23.

A malformation syndrome with ring D chromosome.

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Infant male with ring chromosome 14.

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[Description of a case of multiple malformative syndrome with abnormality of a chromosome of the D group].

Minerva Pediatr. 1969 Jun 2;21(22):1009-13.

[Clinical diagnosis of the phenotype corresponding to a ring-shaped D chromosome].

Presse Med (1893). 1970 Apr 25;78(21):955-8.

Ring chromosome 15.

Acta Paediatr Acad Sci Hung. 1982;23(4):409-15.

[Trial classification of D group chromosome long arm deletions. Apropos of a 15q- case].

Ann Genet. 1971 Mar;14(1):33-40.

引用本文的文献

Inheritance of a ring 14 chromosome.

J Med Genet. 1981 Jun;18(3):209-13. doi: 10.1136/jmg.18.3.209.

13q-/r(13) mosaicism.

Eur J Pediatr. 1981 Mar;136(1):101-4. doi: 10.1007/BF00441721.

Study of two cases of ring 13 chromosome using high-resolution banding.

Am J Hum Genet. 1981 Mar;33(2):252-61.

The ring chromosome 13 syndrome.

Hum Genet. 1982;61(1):18-23. doi: 10.1007/BF00291324.

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

Hum Genet. 1984;67(1):86-93. doi: 10.1007/BF00270563.

Malformative syndrome with ring chromosome 13.

Humangenetik. 1974;24(3):235-40. doi: 10.1007/BF00283592.

The behavior of ring chromosome 13.

Humangenetik. 1974;24(3):161-71. doi: 10.1007/BF00283581.

Clinical features in a case with ring chromosome 13.

Eur J Pediatr. 1985 Nov;144(4):409-12. doi: 10.1007/BF00441791.

Familial ring (20) chromosomal mosaicism.

Hum Genet. 1989 Sep;83(2):148-54. doi: 10.1007/BF00286708.

Ring chromosome 13: lack of distinct syndromes based on different breakpoints on 13q.

J Med Genet. 1992 Oct;29(10):704-8. doi: 10.1136/jmg.29.10.704.

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