| no |
title |
author |
magazine |
year |
volume |
issue |
page(s) |
type |
| 1 |
A rare case: mosaic trisomy 22
|
Basaran, Nurettin
|
|
2001
|
44 |
4 |
p. 183-186
4 p.
|
article
|
| 2 |
Author index
|
|
|
2001
|
44 |
4 |
p. 219-220
2 p.
|
article
|
| 3 |
Contribution of ultrasonographic examination to the prenatal detection of chromosomal abnormalities in 19 centres across Europe
|
De Vigan, C
|
|
2001
|
44 |
4 |
p. 209-217
9 p.
|
article
|
| 4 |
Deletion screening by fluorescence in situ hybridization in Rett syndrome patients
|
Bourdon, Violaine
|
|
2001
|
44 |
4 |
p. 191-194
4 p.
|
article
|
| 5 |
Del Xq23 in a Mosaic Turner Female: Molecular and Cytogenetic Studies
|
Mesa-Cornejo, Viviana Matilde
|
|
2001
|
44 |
4 |
p. 171-174
4 p.
|
article
|
| 6 |
Duplication 8 〚inv dup(8)(p12p23)〛 with macrocephaly
|
Tonk, Vijay S.
|
|
2001
|
44 |
4 |
p. 195-199
5 p.
|
article
|
| 7 |
Further clinical delineation in trisomy 1q32 syndrome
|
Nuño-Arana, Ismael
|
|
2001
|
44 |
4 |
p. 175-177
3 p.
|
article
|
| 8 |
Keyword index
|
|
|
2001
|
44 |
4 |
p. 221-224
4 p.
|
article
|
| 9 |
18p deletion syndrome with a 45, XY, t (14; 18) (p11;q11.2), -18, karyotype
|
Babu Rao, Vunditi
|
|
2001
|
44 |
4 |
p. 187-190
4 p.
|
article
|
| 10 |
Risk factors in congenital abdominal wall defects (omphalocele and gastroschisi): a study in a series of 265 858 consecutive births
|
Stoll, C.
|
|
2001
|
44 |
4 |
p. 201-208
8 p.
|
article
|
| 11 |
Second trimester prenatal diagnosis of epignathus teratoma in ring X chromosome mosaicism with inactive ring X chromosome
|
Witters, Ingrid
|
|
2001
|
44 |
4 |
p. 179-182
4 p.
|
article
|
| 12 |
Y-chromosome mosaicism with ring Y-chromosome/idic(Y)(p11.2) and “normal” ovarian development
|
Fryns, J.P
|
|
2001
|
44 |
4 |
p. 169-
1 p.
|
article
|
Journal description