Поисковый запрос: (<.>S=ГОЛОПРОЗЕНЦЕФАЛИЯ<.>) |
Общее количество найденных документов : 9
Показаны документы с 1 по 9
|
1.
| Prenatal diagnosis of de novo proximal interstitial deletion of 14q associated with cebocephaly // J. Med. Genet., 1997. Vol. 34, N 9.-С.777-778
|
2.
| Molecular cytogenetic analysis of patients with holoprosencephaly and structural rearrangements of 7q // Amer. J. Med. Genet., 1998. Vol. 76, N 1.-С.51-57
|
3.
| Agnathia-holoprosencephaly-situs inversus // Amer. J. Med. Genet., 2000. Vol. 91, N 3.-С.235-236
|
4.
| Holoprosencephaly, hypertelorism, and ectrodactyly in a boy with an apparently balanced de novo t(2;4)(q14.2;q35) // Amer. J. Med. Genet., 2000. Vol. 90, N 5.-С.423-426
|
5.
| Barr Holoprosencephaly survival and performance // Amer. J. Med. Genet., 1999. Vol. 89, N 2.-С.116-120
|
6.
| Cohen M.Michael Problems in the definition of holoprosencephaly // Amer. J. Med. Genet., 2001. Vol. 103, N 3.-С.183-187
|
7.
| Cohen M.Michael Problems in the definition of holoprosencephaly // Amer. J. Med. Genet., 2001. Vol. 103, N 3.-С.183-187
|
8.
| Molecular diagnosis of a novel heterozygous 268C'->'T (R90C) mutation in TGIF gene in a fetus with holoprosencephaly and premaxillary agenesis // Prenat. Diagn., 2002. Vol. 22, N 1.-С.5-7
|
9.
| Sakala Elmar P. Fundal uterine leiomyoma obscuring first-trimester transabdominal sonographic diagnosis of fetal holoprosencephaly: A case report // J. Reprod. Med., 1993. Vol. 38, N 5.-С.400-402
|
|
|
Главная
Назад
"Электронные каталоги и базы данных библиотек СО РАН"