List of bibliographic references indexed by developmental
Number of relevant bibliographic references: 32.
[20-40] [
0 - 20][
0 - 32]
| Ident. | Authors (with country if any) | Title |
|---|
| 00CA97 (1994) |
P W Buss [Royaume-Uni] | Cleft hand/foot: clinical and developmental aspects. |
| 00CC66 (1993) |
R. Greenlee ; H. Hoyme ; M. Witte ; P. Crowe ; C. Witte | Developmental disorders of the lymphatic system. |
| 00CF35 (1993) |
Wei-Sean Winter [Royaume-Uni] | Distinctive autosomal or X‐linked dominant syndrome of microcephaly, mild developmental delay, short stature, and distinctive face |
| 00CF39 (1993) |
V. Gross-Tsur [Israël] ; O. Manor [Israël] ; R S Shalev [Israël] | Developmental dyscalculia, gender, and the brain. |
| 00D831 (1991) |
N J Shaw ; D. Haigh ; G T Lealmann ; G. Karbani ; J T Brocklebank ; M J Dillon | Autosomal recessive hypoparathyroidism with renal insufficiency and developmental delay. |
| 00D998 (1990) |
N B Piller [Australie] | Macrophage and tissue changes in the developmental phases of secondary lymphoedema and during conservative therapy with benzopyrone. |
| 00DC68 (1990) |
Inge Buntinx [Belgique] ; Inge Majewski [Allemagne] | Blepharophimosis, iris coloboma, microgenia, hearing loss, postaxial polydactyly, aplasia of corpus callosum, hydroureter, and developmental delay |
| 00E539 (1987) |
W C Marsch | [Stewart-Treves syndrome: hemangiosarcoma in chronic lymphedema. Ultrastructural analysis of various clinical developmental stages]. |
| 00E570 (1987) |
F T Shi ; X F Luo | [Detection of serum antibodies in bancroftian filariasis patients with antigens from different developmental stages of Brugia malayi]. |
| 00F792 (1982) |
Manuel Opitz [États-Unis] ; Enid F. Gilbert | CNS anomalies and the midline as a “developmental field” |
| 011610 (1964) |
Harold F. Falls [États-Unis] ; Elsa D. Kertesz [États-Unis] | A New Syndrome Combining Pterygium Colli with Developmental Anomalies of the Eyelids and Lymphatics of the Lower Extremities* |
| 012F87 (????) |
Konrad Oexle [Allemagne] ; Maja Hempel ; Anna Jauch ; Thomas Meitinger ; Núria Rivera-Brugués ; Sabine Stengel-Rutkowski ; Tim Strom | 3.7 Mb tandem microduplication in chromosome 5p13.1-p13.2 associated with developmental delay, macrocephaly, obesity, and lymphedema. Further characterization of the dup(5p13) syndrome. |
Pour manipuler ce document sous Unix (Dilib)
EXPLOR_STEP=$WICRI_ROOT/Wicri/Sante/explor/LymphedemaV1/Data/Main/Exploration
HfdIndexSelect -h $EXPLOR_AREA/Data/Main/Exploration/Title.i -k "developmental"
HfdIndexSelect -h $EXPLOR_AREA/Data/Main/Exploration/Title.i \
-Sk "developmental" \
| HfdSelect -Kh $EXPLOR_AREA/Data/Main/Exploration/biblio.hfd
Pour mettre un lien sur cette page dans le réseau Wicri
{{Explor lien
|wiki= Wicri/Sante
|area= LymphedemaV1
|flux= Main
|étape= Exploration
|type= indexItem
|index= Title.i
|clé= developmental
}}
| This area was generated with Dilib version V0.6.31.
Data generation: Sat Nov 4 17:40:35 2017. Site generation: Tue Feb 13 16:42:16 2024 |  |
