Zobrazeno 1 - 10
of 10
pro vyhledávání: '"Frederick C. Koppitch"'
Publikováno v:
American Journal of Obstetrics and Gynecology. 163:1505-1510
In utero chorionic villus sampling at the time of diagnosis of intrauterine fetal death is compared with more traditional use of cultured fetal skin, products of conception, or amniocentesis. A total of 102 specimens from early fetal losses were eval
Autor:
Virginie Ringa, John C. Fletcher, A. Harkes, Toru Kanzaki, Anthony Rodgers, Atsuyoshi Takao, Gérard Bréart, Jun Murotsuki, M. R. J. Williams, M. Murakami, K. H. Nicolaides, Béatrice Blondel, Fabrice Carrat, Carl V. Felton, Mark I. Evans, Line Leduc, Shiro Kozuma, Akira Yajima, Robert J. Carpenter, Nobuya Unno, David James, Yoshihide Chiba, Hidetaka Endo, Fen-Fen Wu, Frederick C. Koppitch, Kazuo Momma, K. Akiba, Masahiko Ando, Takashi Okai, Shingo Tanigawara, Kunihiro Okamura, Beth Boyer Kollas, Yoshinori Kuwabara, Mark P. Johnson, H. Eddowes, Kenneth J. Moise, Ghassan Azar, Kypros H. Nicolaides, Rosalinde J. M. Snijders, Brian Wigdahl, Norio Shinozuka, Heather T. Hartle, Nelson B. Isada, Lorraine E. Cano, Takanori Watanabe, Masahiko Mizuno, M. Iwamoto, Hideki Kobayashi, Guy Thorpe-Beeston
Publikováno v:
Fetal Diagnosis and Therapy. 5:I-IV
Autor:
Mark P. Johnson, Peter G. Pryde, Nelson B. Isada, Mark I. Evans, Frederick C. Koppitch, Mishun D. Childs, Alfred G. Robichaux
Publikováno v:
Fetal diagnosis and therapy. 8(2)
Increasing utilization of chorionic villus sampling (CVS) has lead to the discovery that the placenta can karyotypically be a very heterogeneous organ, and chromosomal mosaicism within the placental can confuse cytogenetic interpretation. Recently, c
Autor:
Frederick C. Koppitch, Mark I. Evans, Joyce Moody, Yoram Sorokin, Wendy R. Uhlmann, I E Zador, Mark P. Johnson, Arie Drugan
Publikováno v:
American journal of medical genetics. 39(3)
We performed chorionic villus samplings (CVS) in 795 cases in the first trimester during a 13-month period. Of these 35 were found to have a blighted ovum or missed abortion prior to the procedure. Nineteen women consented to have CVS. Ultrasonograph
Publikováno v:
Fetal diagnosis and therapy. 5(3-4)
Second trimester amniotic fluid (AF) is generally clear or very light yellow. We examined the color of 2,141 AF samples. Fifty-six specimens were brown, 35 were green. There were 71 samples with abnormal karyotype (3.46%). In the group with brown AF,
Publikováno v:
American Journal of Obstetrics and Gynecology. 154:408-411
Low cytogenetic yields in the processing of small chorionic villus sampling have in some instances, limited its applicability. We have modified “standard” techniques to increase the number of interpretable metaphases by (1) using a gravity method
Publikováno v:
Fetal Diagnosis and Therapy. 4:178-184
In 7 second trimester pregnancies ultrasound (US) demonstrated cystic hygroma colli (CHC); amniocentesis was performed in 6 patients. In the 7th patient, because of oli-gohydramnios, the fluid for karyotype was aspirated from the CHC. Five pregnancie
Autor:
Akifumi Kagiya, Kamran S. Moghissi, Y. Eguchi, Frederick C. Koppitch, Andrea L. Tranquilli, Menq Jer Lee, Arie Drugan, Deborah A. Mitchell, A. Schoenfeld, Masafumi Yamamoto, Mark I. Evans, Robert A. Kanfmann, K. Arishima, Yoram Sorokin, Massimo Boemi, Giuseppe de Tommaso, Alexander Neri, Y. Pardon, Paolo Fumelli, R. Zaizov, Ian J. Cohen, Sidney F. Bottoms, Tatsno Tachizaki, Herbert Valensise, Narihiro Echizenya, Carlo Romanini, Mark P. Johnson, Yoshiharu Saito, Yoav Ben-Yoseph, Garzetti Gg
Publikováno v:
Fetal Diagnosis and Therapy. 4:I-V
Publikováno v:
Prenatal Diagnosis. 6:69-73
Second trimester amniocentesis has traditionally been utilized for prenatal genetic diagnosis. Chorionic villi sampling (CVS) is presently offered as an alternative. The occurrence of fetomaternal bleed (FMB) during CVS could increase the rate of pos
Publikováno v:
Acta Obstetricia et Gynecologica Scandinavica. 61:34-34
A data base centered on chromosome analysis of amniotic cells is maintained on multiple data base management and statistical analysis systems. The data are collected from patients referred for karyotyping and genetic counseling either to the Wayne St