Zobrazeno 1 - 8
of 8
pro vyhledávání: '"Lita Alonso"'
Autor:
Ken McElreavey, Susan Matthew, Berrin Ergun-Longmire, Lita Alonso, Susan Tansil, Karen Lin-Su, Maria I. New, Giovanna Vinci
Publikováno v:
Journal of pediatric endocrinologymetabolism : JPEM. 18(8)
The main factor influencing the sex determination of an embryo is the genetic sex determined by the presence or absence of the Y chromosome. However, some individuals carry a Y chromosome but are phenotypically female (46,XY females) or have a female
Autor:
Jane Lin, Takahiro Nakano, Jian Kang, Weiguo Peng, Melissa K. Carpenter, M. Lita Alonso, Neeta S. Roy, H. Michael Keyoung, Martha S. Windrem, Steven A. Goldman, William K. Rashbaum
Publikováno v:
Nature biotechnology. 22(3)
Lineage-restricted progenitors of the central nervous system (CNS) are not readily expandable because their mitotic competence is limited. Here we used retroviral overexpression of human telomerase reverse transcriptase (hTERT) to immortalize progeni
Publikováno v:
Prenatal diagnosis. 21(1)
X chromosome deletion is an infrequent finding in prenatal diagnosis and presents a difficult counseling challenge when it occurs. We present a case of a familial X chromosome long arm deletion discovered in a routine amniocentesis and subsequently i
Autor:
Beth A. Pletcher, Maureen M. Sanz, James H. Ray, W. Ted Brown, Suphat Kunaporn, Jerrold S. Schlessel, Ann-Leslie Zaslav, Martin G. Bialer, Carrie McKenna, M. Lita Alonso
Publikováno v:
Prenatal diagnosis. 14(10)
Two phenotypically abnormal liveborns in whom trisomy 16 mosaicism was diagnosed prenatally by amniocentesis are described. Analysis of a percutaneous umbilical blood sample in one case revealed a normal chromosomal complement. Ultrasound examination
Autor:
Ernest Lieber, Lawrence R. Shapiro, Peter Benn, Karen David, Edmund C. Jenkins, Edward Schutta, Dorothy Warburton, Lita Alonso, Kurt Hirschhorn, Sara Kaffe, Alan Shanske, Lillian Y. F. Hsu
Publikováno v:
Prenatal diagnosis. 12(7)
Currently, accepted protocol which has been developed at the Prenatal Diagnosis Laboratory of New York City (PDL) requires that when a chromosome abnormality is found in one or more cells in one flask, another 20-40 cells must be examined from one or
Publikováno v:
Genetics in Medicine. 2:91
OBJECTIVE: To describe the different types of double trisomies diagnosed in spontaneous abortions. STUDY DESIGN: Retrospective review of spontaneous abortions with double trisomies, 1989-99. Maternal reproductive history was obtained by physician con
Autor:
Susanna Cunningham-Rundles, M. Lita Alonso, Mathilde Krim, Thomas C. Gunby, Craig E. Metroka, Marilyn S. Pollack, John Mihran Davis, Steven S. Witkin, Janet Mouradian, Joseph Sonnabend
Publikováno v:
Annals of the New York Academy of Sciences. 437
Publikováno v:
Genetics in Medicine; January 2000, Vol. 2 Issue: 1 p91-91, 1p