SCOPUS 정보 검색 플랫폼

Research Communications in Molecular Pathology and Pharmacology

Volumn 94, Issue 3, 1996, Pages 323-326

Chromosome abnormalities associated with recurrent abortion

Author keywords

[No Author keywords available]

Indexed keywords

ADULT; ARTICLE; CHROMOSOME ABERRATION; CHROMOSOME ANALYSIS; CHROMOSOME INVERSION; CHROMOSOME TRANSLOCATION; FEMALE; GENETIC ANALYSIS; HUMAN; MAJOR CLINICAL STUDY; MALE; PRIORITY JOURNAL; RECURRENT ABORTION;

ABORTION, HABITUAL; ADULT; CHROMOSOME ABERRATIONS; FEMALE; HUMANS; INVERSION, CHROMOSOME; KARYOTYPING; MALE; PREGNANCY;

EID: 0030515932 PISSN: 10780297 EISSN: None Source Type: Journal
DOI: None Document Type: Article

Times cited : (3)

References (7)

1
- 0016316563
- Pericentric inversions of human chromosomes 9 and 10
- De La Chapella, A., Schröder, J., Stenstrand, K., Fellman, J., Herba, R., Saarni, M., Anttolainen, L, Tallila, I., Tervilä, L., Husa, L., Tallqvist, G., Robson, E.B., Cook, P.J.L. and Sanger, R. (1974). Pericentric inversions of human chromosomes 9 and 10. Am. J. Hum. Genet. 26: 746-766.
- (1974) Am. J. Hum. Genet. , vol.26 , pp. 746-766
- De La Chapella, A.¹ Schröder, J.² Stenstrand, K.³ Fellman, J.⁴ Herba, R.⁵ Saarni, M.⁶ Anttolainen, L.⁷ Tallila, I.⁸ Tervilä, L.⁹ Husa, L.¹⁰ Tallqvist, G.¹¹ Robson, E.B.¹² Cook, P.J.L.¹³ Sanger, R.¹⁴

2
- 0020029734
- An attempt to define 1qh+, 9qh+ and 16qh+
- Friedrich, U. and Therkelsen, A.J. (1982). An attempt to define 1qh+, 9qh+ and 16qh+. Hum. Genet. 60: 139-144.
- (1982) Hum. Genet. , vol.60 , pp. 139-144
- Friedrich, U.¹ Therkelsen, A.J.²

3
- 0015970098
- Frequency of 9qh+ and risk of chromosome aberrations in the pregnancy of individuals with 9qh+
- Nielsen, J., Friedrich, U., Hreidarsson, A.B. and Veuthen, E. (1974). Frequency of 9qh+ and risk of chromosome aberrations in the pregnancy of individuals with 9qh+. Hum. Genet. 21: 211-215.
- (1974) Hum. Genet. , vol.21 , pp. 211-215
- Nielsen, J.¹ Friedrich, U.² Hreidarsson, A.B.³ Veuthen, E.⁴

4
- 0016260744
- Chromosome study of couples with repeated spontaneous abortions
- Papp, Z., Gardo, S. and Dolhay, B. (1974). Chromosome study of couples with repeated spontaneous abortions. Fertil. Steril. 25: 713-716.
- (1974) Fertil. Steril. , vol.25 , pp. 713-716
- Papp, Z.¹ Gardo, S.² Dolhay, B.³

5
- 17644444070
- Two pericentric inversions inv (7)(p15;q32) and inv (9)(p11;q13) in a male with absence of vas deferens
- Petit, P. and Fryns, J.P. (1983). Two pericentric inversions inv (7)(p15;q32) and inv (9)(p11;q13) in a male with absence of vas deferens. Hum. Genet. 64: 303-306.
- (1983) Hum. Genet. , vol.64 , pp. 303-306
- Petit, P.¹ Fryns, J.P.²

6
- 0020405366
- Chromosome polymorphism in 110 couples with reproductive failure and subsequent pregnancy outcome
- Tho, S.P., Byrd, J.R. and McDonough, P.G. (1982). Chromosome polymorphism in 110 couples with reproductive failure and subsequent pregnancy outcome. Fertil. Steril. 38: 688-694.
- (1982) Fertil. Steril. , vol.38 , pp. 688-694
- Tho, S.P.¹ Byrd, J.R.² McDonough, P.G.³

7
- 0017282479
- Chromosome studies in couples with repeated spontaneous abortions
- Tsenghi, C., Metaxotou-Stavridak, C., Stratakibenetou, M., Kalpini-Mavrou, A. and Matsaniotis, N. (1976). Chromosome studies in couples with repeated spontaneous abortions. Obstet. Gynecol. 47: 463-468.
- (1976) Obstet. Gynecol. , vol.47 , pp. 463-468
- Tsenghi, C.¹ Metaxotou-Stavridak, C.² Stratakibenetou, M.³ Kalpini-Mavrou, A.⁴ Matsaniotis, N.⁵

* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.