[父亲染色体4短臂部分三体伴4p-、18q+易位] - Suppr

Suppr

超能文献

[Partial trisomy for the short arm of chromosome 4 with translocation 4p-,18q+ in the father].

作者信息

Schinzel A, Schmid W

出版信息

Humangenetik. 1972;15(2):163-71. doi: 10.1007/BF00295743.

DOI:10.1007/BF00295743

PMID:5049069

Abstract

摘要

相似文献

[Partial trisomy for the short arm of chromosome 4 with translocation 4p-,18q+ in the father].

Humangenetik. 1972;15(2):163-71. doi: 10.1007/BF00295743.

Short-arm deletion, chromosome 4, (4p-), a syndrome?

Ann Hum Genet. 1970 Oct;34(2):137-44. doi: 10.1111/j.1469-1809.1970.tb00227.x.

Transmission of a translocation t(Cp+; Dq-) through three generations; including an example of probable trisomy for the short arm of the C group chromosome No. 9.

Ann Genet. 1969 Mar;12(1):15-27.

[Partial trisomy of the short arm of chromosome 4 due to translocation t(4p-22p+)].

Humangenetik. 1973 May 25;18(3):207-11. doi: 10.1007/BF00290598.

Trisomy 18 associated with a familial translocation t(Bq-; 18q+).

Ann Genet. 1969 Mar;12(1):46-50.

Paternal transmission of a B-D translocation, t(4p-; 14p + or 15p+), resulting in a partial 4p trisomy.

Humangenetik. 1972;16(3):251-9. doi: 10.1007/BF00273472.

Case report. Familial 4-22 translocation with partial trisomy for the short arm of chromosome 4 in two sibs.

Acta Paediatr Scand. 1974 Jul;63(4):631-5. doi: 10.1111/j.1651-2227.1974.tb04860.x.

Partial trisomy 4q and partial monosomy 18q as a consequence of a paternal balanced translocation t(4qminus; 18qplus).

Humangenetik. 1974;25(3):227-33. doi: 10.1007/BF00281431.

Chromosomal rearrangements in three generations of a Jamaican family. A possible further example of recombinational imbalance.

Cytogenetics. 1970;9(5):360-8. doi: 10.1159/000130105.

Partial trisomy 4 resulting from a 4-18 reciprocal translocation.

Ann Genet. 1972 Sep;15(3):191-4.

引用本文的文献

Trisomy 4p and partial monosomy 18q due to paternal translocation t(4;18) (p11; q21.3).

Indian J Pediatr. 2000 Aug;67(8):601-4. doi: 10.1007/BF02758495.

Clinical manifestations of trisomy 4p syndrome.

Eur J Pediatr. 1995 Jun;154(6):425-31. doi: 10.1007/BF02029349.

The trisomy 4p syndrome: a case report.

Eur J Pediatr. 1982 May;138(3):273-5. doi: 10.1007/BF00441217.

Selective IgA deficiency with 18q+ and 18q-- karyotypic anomalies.

J Med Genet. 1980 Dec;17(6):453-6. doi: 10.1136/jmg.17.6.453.

[Partial trisomy of the short arm of chromosome 4 due to translocation t(4p-22p+)].

Humangenetik. 1973 May 25;18(3):207-11. doi: 10.1007/BF00290598.

Multiple congenital defects associated with trisomy for the short arm of chromosome 4.

J Med Genet. 1974 Sep;11(3):291-5. doi: 10.1136/jmg.11.3.291.

The radiological pattern associated with the trisomy of the short arm of chromosome No 4.

Pediatr Radiol. 1975 Jan 24;3(1):34-40. doi: 10.1007/BF00973364.

[Trisomy 4p. Three new observations (author's transl)].

Humangenetik. 1975 Nov 6;30(2):99-108. doi: 10.1007/BF00291941.

Trisomy 4p14 leads to 4pter with translocation t(4;15)(p14;p12) in the father.

Humangenetik. 1975 Oct 7;29(4):329-35. doi: 10.1007/BF00394195.

A case of trisomy of the short arms of chromosome no. 4 with translocation t(4p 21p; 4q 21q) in the mother.

Humangenetik. 1975;26(2):87-91. doi: 10.1007/BF00278433.

本文引用的文献

[PARTIAL MONOSOMY FOR A SMALL ACROCENTRIC CHROMOSOME].

C R Hebd Seances Acad Sci. 1964 Nov 30;259:4187-90.

A 4-5/21-22 CHROMOSOMAL TRANSLOCATION ASSOCIATED WITH MULTIPLE CONGENITAL ANOMALIES.

Acta Paediatr (Stockh). 1964 Mar;53:172-81. doi: 10.1111/j.1651-2227.1964.tb07224.x.

Chromosome preparations of leukocytes cultured from human peripheral blood.

Exp Cell Res. 1960 Sep;20:613-6. doi: 10.1016/0014-4827(60)90138-5.

Translocation heterozygosis: a cause of five cases of the cri du chat syndrome and two cases with a duplication of chromosome number five in three families.

Am J Hum Genet. 1967 Jul;19(4):586-603.

Statistical analysis of the normal human karyotype.

Am J Hum Genet. 1969 Jul;21(4):322-51.

Clinical and chromosomal studies of the 18q- syndrome.

J Pediatr. 1971 Jan;78(1):44-52. doi: 10.1016/s0022-3476(71)80262-7.

Inherited pericentric inversion of chromosome no. 4.

Am J Hum Genet. 1970 Nov;22(6):679-90.

A pedigree of 4/18 translocation chromosomes with type and countertype partial trisomy and partal monosomy for chromosome 18.

Ann Genet. 1967 Dec;10(4):159-66.

[Genetic and clinical study of a family of 7 children in which 3 persons have "crying cat syndrome"].

Ann Genet. 1966 Sep;9(3):113-22.

[Partial deletion of the long arm of chromosome 18. Individualization of a new morbid state].

Ann Genet. 1966;9(1):32-8.

文献AI研究员

20分钟写一篇综述，助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型，支持多种主流文档格式。

立即体验

[Partial trisomy for the short arm of chromosome 4 with translocation 4p-,18q+ in the father].

作者信息

Schinzel A, Schmid W

出版信息

Humangenetik. 1972;15(2):163-71. doi: 10.1007/BF00295743.

DOI:10.1007/BF00295743

PMID:5049069

Abstract

摘要

相似文献

[Partial trisomy for the short arm of chromosome 4 with translocation 4p-,18q+ in the father].

Humangenetik. 1972;15(2):163-71. doi: 10.1007/BF00295743.

Short-arm deletion, chromosome 4, (4p-), a syndrome?

Ann Hum Genet. 1970 Oct;34(2):137-44. doi: 10.1111/j.1469-1809.1970.tb00227.x.

Transmission of a translocation t(Cp+; Dq-) through three generations; including an example of probable trisomy for the short arm of the C group chromosome No. 9.

Ann Genet. 1969 Mar;12(1):15-27.

[Partial trisomy of the short arm of chromosome 4 due to translocation t(4p-22p+)].

Humangenetik. 1973 May 25;18(3):207-11. doi: 10.1007/BF00290598.

Trisomy 18 associated with a familial translocation t(Bq-; 18q+).

Ann Genet. 1969 Mar;12(1):46-50.

Paternal transmission of a B-D translocation, t(4p-; 14p + or 15p+), resulting in a partial 4p trisomy.

Humangenetik. 1972;16(3):251-9. doi: 10.1007/BF00273472.

Case report. Familial 4-22 translocation with partial trisomy for the short arm of chromosome 4 in two sibs.

Acta Paediatr Scand. 1974 Jul;63(4):631-5. doi: 10.1111/j.1651-2227.1974.tb04860.x.

Partial trisomy 4q and partial monosomy 18q as a consequence of a paternal balanced translocation t(4qminus; 18qplus).

Humangenetik. 1974;25(3):227-33. doi: 10.1007/BF00281431.

Chromosomal rearrangements in three generations of a Jamaican family. A possible further example of recombinational imbalance.

Cytogenetics. 1970;9(5):360-8. doi: 10.1159/000130105.

Partial trisomy 4 resulting from a 4-18 reciprocal translocation.

Ann Genet. 1972 Sep;15(3):191-4.

引用本文的文献

Trisomy 4p and partial monosomy 18q due to paternal translocation t(4;18) (p11; q21.3).

Indian J Pediatr. 2000 Aug;67(8):601-4. doi: 10.1007/BF02758495.

Clinical manifestations of trisomy 4p syndrome.

Eur J Pediatr. 1995 Jun;154(6):425-31. doi: 10.1007/BF02029349.

The trisomy 4p syndrome: a case report.

Eur J Pediatr. 1982 May;138(3):273-5. doi: 10.1007/BF00441217.

Selective IgA deficiency with 18q+ and 18q-- karyotypic anomalies.

J Med Genet. 1980 Dec;17(6):453-6. doi: 10.1136/jmg.17.6.453.

[Partial trisomy of the short arm of chromosome 4 due to translocation t(4p-22p+)].

Humangenetik. 1973 May 25;18(3):207-11. doi: 10.1007/BF00290598.

Multiple congenital defects associated with trisomy for the short arm of chromosome 4.

J Med Genet. 1974 Sep;11(3):291-5. doi: 10.1136/jmg.11.3.291.

The radiological pattern associated with the trisomy of the short arm of chromosome No 4.

Pediatr Radiol. 1975 Jan 24;3(1):34-40. doi: 10.1007/BF00973364.

[Trisomy 4p. Three new observations (author's transl)].

Humangenetik. 1975 Nov 6;30(2):99-108. doi: 10.1007/BF00291941.

Trisomy 4p14 leads to 4pter with translocation t(4;15)(p14;p12) in the father.

Humangenetik. 1975 Oct 7;29(4):329-35. doi: 10.1007/BF00394195.

A case of trisomy of the short arms of chromosome no. 4 with translocation t(4p 21p; 4q 21q) in the mother.

Humangenetik. 1975;26(2):87-91. doi: 10.1007/BF00278433.

本文引用的文献

[PARTIAL MONOSOMY FOR A SMALL ACROCENTRIC CHROMOSOME].

C R Hebd Seances Acad Sci. 1964 Nov 30;259:4187-90.

A 4-5/21-22 CHROMOSOMAL TRANSLOCATION ASSOCIATED WITH MULTIPLE CONGENITAL ANOMALIES.

Acta Paediatr (Stockh). 1964 Mar;53:172-81. doi: 10.1111/j.1651-2227.1964.tb07224.x.

Chromosome preparations of leukocytes cultured from human peripheral blood.

Exp Cell Res. 1960 Sep;20:613-6. doi: 10.1016/0014-4827(60)90138-5.

Translocation heterozygosis: a cause of five cases of the cri du chat syndrome and two cases with a duplication of chromosome number five in three families.

Am J Hum Genet. 1967 Jul;19(4):586-603.

Statistical analysis of the normal human karyotype.

Am J Hum Genet. 1969 Jul;21(4):322-51.

Clinical and chromosomal studies of the 18q- syndrome.

J Pediatr. 1971 Jan;78(1):44-52. doi: 10.1016/s0022-3476(71)80262-7.

Inherited pericentric inversion of chromosome no. 4.

Am J Hum Genet. 1970 Nov;22(6):679-90.

A pedigree of 4/18 translocation chromosomes with type and countertype partial trisomy and partal monosomy for chromosome 18.

Ann Genet. 1967 Dec;10(4):159-66.

[Genetic and clinical study of a family of 7 children in which 3 persons have "crying cat syndrome"].

Ann Genet. 1966 Sep;9(3):113-22.

[Partial deletion of the long arm of chromosome 18. Individualization of a new morbid state].

Ann Genet. 1966;9(1):32-8.