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7 in total

1. The Greig polysyndactyly-craniofacial dysmorphism syndrome.

Authors: J P Fryns; W Coeck; H van den Berghe
Journal: Eur J Pediatr Date: 1977-11-04 Impact factor: 3.183

2. Sagittal craniostenosis, congenital heart disease, mental deficiency and various dysmorphies in two sibs--a "new" syndrome?

Authors: R A Pfeiffer; H Singer; S Zschiesche
Journal: Eur J Pediatr Date: 1987-01 Impact factor: 3.183

3. Craniofrontonasal dysplasia.

Authors: L Kapusta; H G Brunner; B C Hamel
Journal: Eur J Pediatr Date: 1992-11 Impact factor: 3.183

4. Greig syndrome associated with an interstitial deletion of 7p: confirmation of the localization of Greig syndrome to 7p13.

Authors: A L Pettigrew; F Greenberg; C T Caskey; D H Ledbetter
Journal: Hum Genet Date: 1991-08 Impact factor: 4.132

5. The Greig polysyndactyly craniofacial dysmorphism syndrome: variable expression in a family.

Authors: J P Fryns; G Van Noyen; H Van den Berghe
Journal: Eur J Pediatr Date: 1981-05 Impact factor: 3.183

6. The spectrum of hand and foot malformations in patients with Greig cephalopolysyndactyly.

Authors: Philippe Debeer; Koen Devriendt; Luc De Smet; Thomy Deravel; Antonio Gonzalez-Meneses; Karl-Heinz Grzeschik; Jean-Pierre Fryns
Journal: J Child Orthop Date: 2007-05-10 Impact factor: 1.548

7. Metopic and sagittal synostosis in Greig cephalopolysyndactyly syndrome: five cases with intragenic mutations or complete deletions of GLI3.

Authors: Jane A Hurst; Dagan Jenkins; Pradeep C Vasudevan; Maria Kirchhoff; Flemming Skovby; Claudine Rieubland; Sabina Gallati; Olaf Rittinger; Peter M Kroisel; David Johnson; Leslie G Biesecker; Andrew O M Wilkie
Journal: Eur J Hum Genet Date: 2011-02-16 Impact factor: 4.246

7 in total