Clinical and molecular-cytogenetic studies of cryptic chromosome aberration in individuals with idiopathic mental retardation and multiple congenital malformations

Radka E. Stoeva; Liliana I. Grazdanova; Joris R. Vermeesch; Maria Kirshhoff; Jean-Pierre Fryns; Ivan S. Ivanov; Iliana H. Patcheva; Boyan I. Dimitrov; Tsanyu B. Krastev; Alexander J. Linev; Margarita T. Stefanova

A 512

Детайли

Източник

Folia Medica

Местоиздаване

Plovdiv

Година на издаване

2008

Пор.№

Страници

55-62

Класификационен индекс

УДК	Значение
616-007.8	Уродства /сложни, двойни и др. /
616.899	Задръжка в умственото развитие. Слабоумие

Том

Ключови думи

Автори от МУ - Пловдив

Допълнителна информация

Системен №: 27144
Тематични рубрики: Педиатрия

Действия

APA Chicago / Turabian (16th edition) Harvard MLA (7th edition)

Stoeva, R., Grazdanova, L., Vermeesch, J., Kirshhoff, M., Fryns, J., Ivanov, I., Patcheva, I., Dimitrov, B., Krastev, T., Linev, A., Stefanova, M. Clinical and molecular-cytogenetic studies of cryptic chromosome aberration in individuals with idiopathic mental retardation and multiple congenital malformations, , 2008, 55-62.

Stoeva, R., Grazdanova, L., Vermeesch, J., Kirshhoff, M., Fryns, J., Ivanov, I., Patcheva, I., Dimitrov, B., Krastev, T., Linev, A., Stefanova, M. . Clinical and molecular-cytogenetic studies of cryptic chromosome aberration in individuals with idiopathic mental retardation and multiple congenital malformations. Plovdiv: , 2008, 55-62.

Stoeva, R., Grazdanova, L., Vermeesch, J., Kirshhoff, M., Fryns, J., Ivanov, I., Patcheva, I., Dimitrov, B., Krastev, T., Linev, A., Stefanova, M. (2008) Clinical and molecular-cytogenetic studies of cryptic chromosome aberration in individuals with idiopathic mental retardation and multiple congenital malformations, Plovdiv: , 55-62

Stoeva, R., Grazdanova, L., Vermeesch, J., Kirshhoff, M., Fryns, J., Ivanov, I., Patcheva, I., Dimitrov, B., Krastev, T., Linev, A., & Stefanova, M. (2008). Clinical and molecular-cytogenetic studies of cryptic chromosome aberration in individuals with idiopathic mental retardation and multiple congenital malformations. Folia Medica. Plovdiv: 50 (4), 55-62.