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A cytogenetic study of recurrent abortion.

作者信息

Bhasin M K, Foerster W, Fuhrmann W

出版信息

Humangenetik. 1973 Apr 16;18(2):139-48. doi: 10.1007/BF00291481.

DOI:10.1007/BF00291481

PMID:4578384

Abstract

摘要

相似文献

A cytogenetic study of recurrent abortion.

Humangenetik. 1973 Apr 16;18(2):139-48. doi: 10.1007/BF00291481.

[Example of the significance of cytogenetic examinations in habitual abortions].

Geburtshilfe Frauenheilkd. 1969 Sep;29(9):792-800.

Cytogenetic aspects of habitual abortion. 1. Chromosome analysis of couples with history of habitual abortion.

Nagoya Med J. 1970 Nov;16(2):59-72.

A prospective, cytogenetic study of recurrent abortion.

J Med Genet. 1969 Mar;6(1):5-13. doi: 10.1136/jmg.6.1.5.

[Cytogenetic aspects of habitual abortion].

Minerva Ginecol. 1986 Mar;38(3):119-25.

Translocation between both members of chromosome pair number 15 causing recurrent abortions.

Ann Hum Genet. 1969 May;32(4):347-52. doi: 10.1111/j.1469-1809.1969.tb00085.x.

[Cytogenetic analysis in couples with spontaneous abortions].

Ginekol Pol. 1997 May;68(5A):248-52.

[Cytogenetic studies on 60 couples with habitual abortions].

Zhongguo Yi Xue Ke Xue Yuan Xue Bao. 1987 Jun;9(3):226-8.

Chromosome abnormalities associated with recurrent abortion.

Res Commun Mol Pathol Pharmacol. 1996 Dec;94(3):323-6.

[Cytogenetic findings in habitual abortion. Chromosomal analysis in 123 couples (author's transl)].

Wien Klin Wochenschr. 1980 Aug 29;92(16):575-8.

引用本文的文献

Determining the Cause of Recurrent Miscarriages in a Couple: Importance of NOR in the Era of NGS.

J Reprod Infertil. 2019 Apr-Jun;20(2):109-114.

A Novel de novo Balanced Reciprocal Translocation t(18;22) Associated with Recurrent Miscarriages: A Case Report.

J Reprod Infertil. 2014 Apr;15(2):113-6.

Pericentric inversion of chromosome 1 in three sterile brothers.

Hum Genet. 1981;58(2):226-7. doi: 10.1007/BF00278718.

Structural differences in pericentric inversions. Application to a model of risk of recombinants.

Hum Genet. 1981;56(3):321-8. doi: 10.1007/BF00274687.

Minor chromosomal variants and major chromosomal anomalies in couples with recurrent abortion.

Am J Hum Genet. 1982 Nov;34(6):948-60.

Balanced translocations among couples with two or more spontaneous abortions: are males and females equally likely to be carriers?

Hum Genet. 1983;63(3):252-7. doi: 10.1007/BF00284659.

Chromosomal findings in 164 couples with repeated spontaneous abortions: with special consideration to prior reproductive history.

Hum Genet. 1983;63(1):28-34. doi: 10.1007/BF00285393.

Familial inv(1) (p3500q21.3) associated with azoospermia.

Hum Genet. 1984;66(2-3):165-7. doi: 10.1007/BF00286593.

Pericentric inversions. Problems and significance for clinical genetics.

Hum Genet. 1984;68(1):1-47. doi: 10.1007/BF00293869.

Familial pericentric and paracentric inversions of chromosome 1.

Hum Genet. 1988 Aug;79(4):315-20. doi: 10.1007/BF00282168.

本文引用的文献

Partial-trisomy syndromes. II. An insertion as cause of the OFD syndrome in mother and daughter.

Chromosoma. 1961;12:573-84. doi: 10.1007/BF00328943.

CHROMOSOME ABNORMALITY AS A POSSIBLE CAUSE OF HABITUAL ABORTION.

Bristol Med Chir J. 1965 Jan;80(1):5-6.

CHROMOSOME STUDIES IN FIVE CASES OF COLOBOMA OF THE IRIS.

Lancet. 1965 Mar 13;1(7385):576-8. doi: 10.1016/s0140-6736(65)91148-7.

DNA REPLICATION PATTERNS OF HUMAN CHROMOSOMES.

Cytogenetics. 1963;2:175-93. doi: 10.1159/000129778.

A FAMILIAL CHROMOSOME VARIANT IN A SUBJECT WITH ANOMALOUS SEX DIFFERENTIATION.

Am J Hum Genet. 1963 Dec;15(4):465-75.

A GENETICAL AND CYTOLOGICAL STUDY OF REPEATED SPONTANEOUS ABORTION.

Ann Hum Genet. 1963 Aug;27:87-100. doi: 10.1111/j.1469-1809.1963.tb00784.x.

Chromosomal study in patients with cysts of the jaw, multiple nevoid basal cell carcinomata and bifid rib syndrome.

Chromosoma. 1963;14:146-53. doi: 10.1007/BF00336756.

A familial chromosome abnormality associated with repeated abortions.

Cytogenetics. 1962;1:199-209. doi: 10.1159/000129729.

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.

Chromosome anomalies as a cause of spontaneous abortion.

Am J Obstet Gynecol. 1967 Feb 1;97(3):283-93. doi: 10.1016/0002-9378(67)90488-7.

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A cytogenetic study of recurrent abortion.

作者信息

Bhasin M K, Foerster W, Fuhrmann W

出版信息

Humangenetik. 1973 Apr 16;18(2):139-48. doi: 10.1007/BF00291481.

DOI:10.1007/BF00291481

PMID:4578384

Abstract

摘要

相似文献

A cytogenetic study of recurrent abortion.

Humangenetik. 1973 Apr 16;18(2):139-48. doi: 10.1007/BF00291481.

[Example of the significance of cytogenetic examinations in habitual abortions].

Geburtshilfe Frauenheilkd. 1969 Sep;29(9):792-800.

Cytogenetic aspects of habitual abortion. 1. Chromosome analysis of couples with history of habitual abortion.

Nagoya Med J. 1970 Nov;16(2):59-72.

A prospective, cytogenetic study of recurrent abortion.

J Med Genet. 1969 Mar;6(1):5-13. doi: 10.1136/jmg.6.1.5.

[Cytogenetic aspects of habitual abortion].

Minerva Ginecol. 1986 Mar;38(3):119-25.

Translocation between both members of chromosome pair number 15 causing recurrent abortions.

Ann Hum Genet. 1969 May;32(4):347-52. doi: 10.1111/j.1469-1809.1969.tb00085.x.

[Cytogenetic analysis in couples with spontaneous abortions].

Ginekol Pol. 1997 May;68(5A):248-52.

[Cytogenetic studies on 60 couples with habitual abortions].

Zhongguo Yi Xue Ke Xue Yuan Xue Bao. 1987 Jun;9(3):226-8.

Chromosome abnormalities associated with recurrent abortion.

Res Commun Mol Pathol Pharmacol. 1996 Dec;94(3):323-6.

[Cytogenetic findings in habitual abortion. Chromosomal analysis in 123 couples (author's transl)].

Wien Klin Wochenschr. 1980 Aug 29;92(16):575-8.

引用本文的文献

Determining the Cause of Recurrent Miscarriages in a Couple: Importance of NOR in the Era of NGS.

J Reprod Infertil. 2019 Apr-Jun;20(2):109-114.

A Novel de novo Balanced Reciprocal Translocation t(18;22) Associated with Recurrent Miscarriages: A Case Report.

J Reprod Infertil. 2014 Apr;15(2):113-6.

Pericentric inversion of chromosome 1 in three sterile brothers.

Hum Genet. 1981;58(2):226-7. doi: 10.1007/BF00278718.

Structural differences in pericentric inversions. Application to a model of risk of recombinants.

Hum Genet. 1981;56(3):321-8. doi: 10.1007/BF00274687.

Minor chromosomal variants and major chromosomal anomalies in couples with recurrent abortion.

Am J Hum Genet. 1982 Nov;34(6):948-60.

Balanced translocations among couples with two or more spontaneous abortions: are males and females equally likely to be carriers?

Hum Genet. 1983;63(3):252-7. doi: 10.1007/BF00284659.

Chromosomal findings in 164 couples with repeated spontaneous abortions: with special consideration to prior reproductive history.

Hum Genet. 1983;63(1):28-34. doi: 10.1007/BF00285393.

Familial inv(1) (p3500q21.3) associated with azoospermia.

Hum Genet. 1984;66(2-3):165-7. doi: 10.1007/BF00286593.

Pericentric inversions. Problems and significance for clinical genetics.

Hum Genet. 1984;68(1):1-47. doi: 10.1007/BF00293869.

Familial pericentric and paracentric inversions of chromosome 1.

Hum Genet. 1988 Aug;79(4):315-20. doi: 10.1007/BF00282168.

本文引用的文献

Partial-trisomy syndromes. II. An insertion as cause of the OFD syndrome in mother and daughter.

Chromosoma. 1961;12:573-84. doi: 10.1007/BF00328943.

CHROMOSOME ABNORMALITY AS A POSSIBLE CAUSE OF HABITUAL ABORTION.

Bristol Med Chir J. 1965 Jan;80(1):5-6.

CHROMOSOME STUDIES IN FIVE CASES OF COLOBOMA OF THE IRIS.

Lancet. 1965 Mar 13;1(7385):576-8. doi: 10.1016/s0140-6736(65)91148-7.

DNA REPLICATION PATTERNS OF HUMAN CHROMOSOMES.

Cytogenetics. 1963;2:175-93. doi: 10.1159/000129778.

A FAMILIAL CHROMOSOME VARIANT IN A SUBJECT WITH ANOMALOUS SEX DIFFERENTIATION.

Am J Hum Genet. 1963 Dec;15(4):465-75.

A GENETICAL AND CYTOLOGICAL STUDY OF REPEATED SPONTANEOUS ABORTION.

Ann Hum Genet. 1963 Aug;27:87-100. doi: 10.1111/j.1469-1809.1963.tb00784.x.

Chromosomal study in patients with cysts of the jaw, multiple nevoid basal cell carcinomata and bifid rib syndrome.

Chromosoma. 1963;14:146-53. doi: 10.1007/BF00336756.

A familial chromosome abnormality associated with repeated abortions.

Cytogenetics. 1962;1:199-209. doi: 10.1159/000129729.

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.

Chromosome anomalies as a cause of spontaneous abortion.

Am J Obstet Gynecol. 1967 Feb 1;97(3):283-93. doi: 10.1016/0002-9378(67)90488-7.