These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.
2. M--craniocarpotarsal dystrophy (whistling face syndrome) in two families. Jorgenson RJ Birth Defects Orig Artic Ser; 1974; 10(5):237-42. PubMed ID: 4220006 [No Abstract] [Full Text] [Related]
3. N--variable expressivity in craniocarpotarsal dysplasia. Wilson CD; Pearce WG Birth Defects Orig Artic Ser; 1974; 10(5):243-8. PubMed ID: 4220007 [No Abstract] [Full Text] [Related]
4. [Noonan's syndrome. Genetic and cardiological study of 2 cases]. Saint-Rome G; Davignon A; Kratz C Union Med Can; 1970 Sep; 99(9):1602-12. PubMed ID: 5005748 [No Abstract] [Full Text] [Related]
6. Syndrome of a craniofacial dysostosis, limb malformation, and omphalocele. Gardner RJ; Morrison PS; Faigan LA; Kennedy JC; Fitzgerald PH Am J Med Genet; 1990 Jun; 36(2):133-6. PubMed ID: 2368799 [TBL] [Abstract][Full Text] [Related]
7. Craniocarpotarsal dysplasia syndrome (whistling face syndrome). Case reports and survey of clinical findings. Burzynski NJ; Podruch PE; Howell J; Snawder K Oral Surg Oral Med Oral Pathol; 1975 Jun; 39(6):893-900. PubMed ID: 806047 [TBL] [Abstract][Full Text] [Related]
8. [Incidence of various congenital abnormalities in patients with Klippel-Feil syndrome]. Kruk J; Kowalewski J Pediatr Pol; 1980 Jan; 55(1):99-106. PubMed ID: 7367074 [No Abstract] [Full Text] [Related]
9. Acrofacial dysostosis with severe facial clefting and limb reduction. Kawira EL; Weaver DD; Bender HA Am J Med Genet; 1984 Mar; 17(3):641-7. PubMed ID: 6711616 [TBL] [Abstract][Full Text] [Related]
10. [The Silver-Russell syndrome]. Bene M; Moga L Rev Pediatr Obstet Ginecol Pediatr; 1980; 29(3):255-63. PubMed ID: 6781034 [No Abstract] [Full Text] [Related]
13. [An unusual syndrome: colobomatous disorder of the eyeball, anal atresia, multiple congenital anomalies and presence of an extra chromosome]. Thomas C; Cordier J; Gilgenkrantz S; Reny A; Raspiller A Ann Ocul (Paris); 1969 Oct; 202(10):1021-31. PubMed ID: 4983376 [No Abstract] [Full Text] [Related]
14. [Congenital glaucoma with dominant heredity associated with ocular and somatic malformations (Rieger's syndrome)]. Deimarcelle Y Ann Ocul (Paris); 1968 Feb; 201(2):132-57. PubMed ID: 4970667 [No Abstract] [Full Text] [Related]
15. Six generations of a family with multiple limb deficiencies. Helal A; Perry T; Ogden JA; Greene TL J Pediatr Orthop; 1993; 13(2):210-3. PubMed ID: 8459013 [TBL] [Abstract][Full Text] [Related]
16. [Frequent familial occurrence of a multiplex malformation of the eye]. Nagy M; Fazekas A Klin Monbl Augenheilkd; 1971 Mar; 158(3):430-7. PubMed ID: 4995582 [No Abstract] [Full Text] [Related]
17. Ocular abnormalities associated with first and second arch syndromes. Feingold M; Gellis SS Surv Ophthalmol; 1969 Jul; 14(1):30-42. PubMed ID: 4980229 [No Abstract] [Full Text] [Related]
18. Whistling-face syndrome. Pahor AL Ear Nose Throat J; 1980 May; 59(5):232-4. PubMed ID: 6771117 [No Abstract] [Full Text] [Related]
19. Freeman Sheldon syndrome in a newborn (whistling face)--a case report. Rao SS; Chary R; Karan S Indian Pediatr; 1979 Mar; 16(3):291-2. PubMed ID: 110675 [No Abstract] [Full Text] [Related]
20. [Congenital functional disorders of the hypothalamus caused by a development disorder of the prosencephalon]. Ceelie N; Steendijk R Tijdschr Kindergeneeskd; 1981 Apr; 49(2):66-73. PubMed ID: 7268757 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]