𝔖 Bobbio Scriptorium
✦   LIBER   ✦

Feingold syndrome: Clinical review and genetic mapping

✍ Scribed by Celli, Jacopo ;van Bokhoven, Hans ;Brunner, Han G.


Publisher
John Wiley and Sons
Year
2003
Tongue
English
Weight
174 KB
Volume
122A
Category
Article
ISSN
0148-7299

No coin nor oath required. For personal study only.


πŸ“œ SIMILAR VOLUMES


Feingold syndrome: Report of a new famil
✍ Courtens, W.; Levi, S.; Verbelen, F.; Verloes, A.; Vamos, E. πŸ“‚ Article πŸ“… 1997 πŸ› John Wiley and Sons 🌐 English βš– 41 KB πŸ‘ 3 views

Feingold syndrome (or oculodigitoesophagoduodenal syndrome; Microcephaly, Mesobrachyphalangy, Tracheo-esophageal fistula syndrome) is a dominantly inherited combination of hand and foot abnormalities, microcephaly, esophageal/duodenal atresia, short palpebral fissures and learning disabilities, firs

Fechtner syndrome: Clinical and genetic
✍ Gershoni-Baruch, R. ;Baruch, Y. ;Viener, A. ;Lichtig, C. ;Opitz, John M. ;Reynol πŸ“‚ Article πŸ“… 1988 πŸ› John Wiley and Sons 🌐 English βš– 791 KB
Clinical and genetic heterogeneity of Se
✍ Faivre, L. ;Le Merrer, M. ;Lyonnet, S. ;Plauchu, H. ;Dagoneau, N. ;Campos-Xavier πŸ“‚ Article πŸ“… 2002 πŸ› John Wiley and Sons 🌐 English βš– 143 KB πŸ‘ 3 views
Genetic and clinical heterogeneity of St
✍ Vintiner, Gillian M. ;Temple, I. Karen ;Middleton-Price, Helen R. ;Baraitser, Mi πŸ“‚ Article πŸ“… 1991 πŸ› John Wiley and Sons 🌐 English βš– 494 KB πŸ‘ 3 views

We have studied 6 multigeneration Stickler syndrome families. Manifestations of the syndrome in the families included myopia, deafness, arthritis, characteristic facial changes with "flat" midface and cleft palate, although not all these were present in all families. COL2Al has been implicated as a