List of bibliographic references
Number of relevant bibliographic references: 11.
| Ident. | Authors (with country if any) | Title |
|---|
| 000E15 (1991) |
O. Gabrielli [Italie] ; C. Catassi ; A. Carlucci ; G. V. Coppa ; P. Giorgi | Intestinal lymphangiectasia, lymphedema, mental retardation, and typical face : confirmation of the Hennekam syndrome |
| 000E26 (1991) |
M. Urioste [Espagne] ; A. Arroyo ; M.-L. Martinez-Frias | Campomelia, polycystic dysplasia, and cervical lymphocele in two sibs |
| 000E32 (1991) |
A. B. Jamjoom [Arabie saoudite] ; B. G. Mathew ; H. B. Coakham | A variant of the syndrome of spinal arachnoid cysts with multiple congential defects |
| 000F04 (1989) |
J. M. Opitz ; J. F. Reynolds ; J. M. Fitzgerald | Mandibulofacial dysostosis or bilateral hemifacial microsomia with hearing loss, telecanthus, tetramelic postaxial hexadactyly, congenital hypotonia and lymphedema with joint hypermobility, and pigmentary dysplasia: a new syndrome? |
| 000F17 (1989) |
R. C. M. Hennekam ; R. A. Geerdink ; B. C. J. Hamel ; F. A. M. Hennekam ; P. Kraus ; J. A. Rammeloo ; A. A. W. Tillemans | Autosomal recessive intestinal lymphangiectasia and lymphedema, with facial anomalies and mental retardation |
| 000F79 (1987) |
S. O. Lewin ; H. E. Hughes | German syndrome in sibs |
| 001030 (1986) |
C. A. Crowe ; L. H. Dickerman | Brief clinical report: a genetic association between microcephaly and lymphedema |
| 001078 (1985) |
A. K. C. Leung | Dominantly inherited syndrome of microcephaly and congenital lymphedema |
| 001079 (1985) |
S. Goldstein ; Q. H. Qazi ; J. Fitzgerald ; J. Goldstein ; A. P. Friedman ; P. Sawyer | Distichiasis, congenital heart defects and mixed peripheral vascular anomalies |
| 001114 (1984) |
S. W. White | Lymphedema in Noonan's syndrome |
| 001142 (1983) |
P. J. Dahlberg ; W. Z. Borer ; K. L. Newcomer ; W. R. Yutuc | Autosomal or X-linked recessive syndrome of congenital lymphedema, hypoparathyroidism, nephropathy, prolapsing mitral valve, and brachytelephalangy |
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