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Items: 9

1.

Chromosome translocations in couples with multiple spontaneous abortions.

Michels VV, Medrano C, Venne VL, Riccardi VM.

Am J Hum Genet. 1982 May;34(3):507-13.

2.

Partial Trisomy 1, Karyotype 46,XY,12-,t(1q,12p)+.

Van den Berghe H, Van Eygen M, Fryns JP, Tanghe W, Verresen H.

Humangenetik. 1973 May 25;18(3):225-30. No abstract available.

PMID:
4719634
3.

Prenatal diagnosis of chromosome abnormalities.

Therkelsen AJ, Petersen GB, Steenstrup OR, Jonasson J, Lindsten J, Zech L.

Acta Paediatr Scand. 1972 Jul;61(4):397-404. No abstract available.

PMID:
4261201
4.

Structural variation in human nitotic chromosomes.

Leisti J.

Ann Acad Sci Fenn Biol. 1971;179:1-69. No abstract available.

PMID:
4261167
5.

Centromere staining at meiosis in man.

Chandley AC, Fletcher JM.

Humangenetik. 1973 May 25;18(3):247-52. No abstract available.

PMID:
4124201
6.

Cytogenetic analysis of 688 couples experiencing multiple spontaneous abortions.

Castle D, Bernstein R.

Am J Med Genet. 1988 Mar;29(3):549-56.

PMID:
3376998
7.

Karyotypes of 1142 couples with recurrent abortion.

Portnoï MF, Joye N, van den Akker J, Morlier G, Taillemite JL.

Obstet Gynecol. 1988 Jul;72(1):31-4.

PMID:
3242501
8.

Recurrent abortions and paternal balanced translocation t(lq--;13q+).

Rozynkowa D, Trebicka-Kwiatkowska B, Stepień, Raczkiewicz B, Krzemiński A.

Humangenetik. 1975 Aug 25;28(4):349-51.

PMID:
1176126
9.

Chromosome studies in couples with repeated spontaneous abortions.

Tsenghi C, Metaxotou-Stavridaki C, Strataki-Benetou M, Kalpini-Mavrou A, Matsaniotis N.

Obstet Gynecol. 1976 Apr;47(4):463-8.

PMID:
943737

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