Risk factors for structural chromosomal abnormality in ≥ 2 miscarriages, as an instrument for selective karyotyping;Risicofactoren voor structurele chromosoomafwijking bij ≥ 2 miskramen als instrument voor selectieve karyotypering
How much difference does chromosome banding make? Adjustments in prevalence and mutation rates of human structural cytogenetic abnormalities
Hook EB, Healy NP, Willey AM. How much difference does chromosome banding make? Adjustments in prevalence and mutation rates of human structural cytogenetic abnormalities. Ann Hum Genet. 1989;53(Pt 3):237-42.
(1989)Ann Hum Genet, vol.53, Issue.PART 3, pp. 237-242
Braekeleer M de, Dao TN. Cytogenetic studies in couples experiencing repeated pregnancy losses. Hum Reprod. 1990;5:519-28.
Braekeleer M de, Dao TN. Cytogenetic studies in couples experiencing repeated pregnancy losses. Hum Reprod. 1990;5:519-28.
3
34248196561
The investigation and treatment of couples with recurrent miscarriage. Guideline 17. Londen: Royal College of Obstetricians and Gynaecologists; 2003.
The investigation and treatment of couples with recurrent miscarriage. Guideline 17. Londen: Royal College of Obstetricians and Gynaecologists; 2003.
4
0036690113
ACOG practice bulletin. Management of recurrent pregnancy loss. Number 24, February 2001
American College of Obstetricians and Gynecologists
American College of Obstetricians and Gynecologists. ACOG practice bulletin. Management of recurrent pregnancy loss. Number 24, February 2001. Int J Gynaecol Obstet. 2002;78:179-90.
Mitelman F, editor. An International System for Human Cytogenetic Nomenclature (ISCN) 1995: recommendations of the International Standing Committee on Human Cytogenetic Nomenclature. Bazel: Karger; 1995.
An informative protocol for the investigation of recurrent miscarriage: Preliminary experience of 500 consecutive cases
Clifford K, Rai R, Watson H, Regan L. An informative protocol for the investigation of recurrent miscarriage: preliminary experience of 500 consecutive cases. Hum Reprod. 1994;9:1328-32.
Data on families of chromosome translocation carriers ascertained because of habitual spontaneous abortion
Smith A, Gaha TJ. Data on families of chromosome translocation carriers ascertained because of habitual spontaneous abortion. Aust N Z J Obstet Gynaecol. 1990;30:57-62.
Sachs ES, Jahoda MG, Hemel JO van, Hoogeboom AJM, Sandkuyl LA. Chromosome studies of 500 couples with two or more abortions. Obstet Gynecol. 1985;65:375-8.
Sachs ES, Jahoda MG, Hemel JO van, Hoogeboom AJM, Sandkuyl LA. Chromosome studies of 500 couples with two or more abortions. Obstet Gynecol. 1985;65:375-8.
* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.