Rare trisomy mosaicism diagnosed in amniocytes, involving an autosome other than chromosomes 13, 18, 20, and 21: karyotype/phenotype correlations.

Autor: Hsu LY; Prenatal Diagnosis Laboratory of New York City/Medical and Health Research Association of N.Y., Inc., NY, USA., Yu MT, Neu RL, Van Dyke DL, Benn PA, Bradshaw CL, Shaffer LG, Higgins RR, Khodr GS, Morton CC, Wang H, Brothman AR, Chadwick D, Disteche CM, Jenkins LS, Kalousek DK, Pantzar TJ, Wyatt P

Publikováno v: Prenatal diagnosis [Prenat Diagn] 1997 Mar; Vol. 17 (3), pp. 201-42.

Incidence and significance of chromosome mosaicism involving an autosomal structural abnormality diagnosed prenatally through amniocentesis: a collaborative study.

Autor: Hsu LY; Prenatal Diagnosis Laboratory of New York City, USA., Yu MT, Richkind KE, Van Dyke DL, Crandall BF, Saxe DF, Khodr GS, Mennuti M, Stetten G, Miller WA, Priest JH

Publikováno v: Prenatal diagnosis [Prenat Diagn] 1996 Jan; Vol. 16 (1), pp. 1-28.

Down's Syndrome Subsequent to Monosomy 21

Autor: Khodr Gs

Publikováno v: New England Journal of Medicine. 304:1366-1367

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6d139529aaa530f969baa449c6df530b
https://doi.org/10.1056/nejm198105283042223

Tento výsledek nelze pro nepřihlášené uživatele zobrazit.
K zobrazení výsledku je třeba se přihlásit.

A Case of a Derivative Chromosome: der(Y)t(Y;18)Pat with Congenital Abnormalities.

Autor: Huang, Shufang^1,2 (AUTHOR), Xia, Yu^3,4 (AUTHOR), Ding, Hong^1,2 (AUTHOR), Wang, Yonghua^1,2 (AUTHOR), Wu, Yueheng^4,5 (AUTHOR), Chen, Shaoxian^4,5 (AUTHOR), Zhuang, Jian^3,4 (AUTHOR), Li, Ping^1,2 (AUTHOR)

Publikováno v: Fetal & Pediatric Pathology. Jun2021, Vol. 40 Issue 3, p256-261. 6p.