160 related articles for article (PubMed ID: 1742043)
1. Whistling face syndrome. A case report and literature review.
Millner MM; Mutz ID; Rosenkranz W
Acta Paediatr Hung; 1991; 31(3):279-89. PubMed ID: 1742043
[TBL] [Abstract][Full Text] [Related]
2. Autosomal recessive form of whistling face syndrome in sibs.
Dallapiccola B; Giannotti A; Lembo A; Saguì L
Am J Med Genet; 1989 Aug; 33(4):542-4. PubMed ID: 2596515
[TBL] [Abstract][Full Text] [Related]
3. [The Freeman-Sheldon Syndrome].
Aldinger G; Eulert J
Z Orthop Ihre Grenzgeb; 1983; 121(5):630-3. PubMed ID: 6649811
[TBL] [Abstract][Full Text] [Related]
4. Further evidence for genetic heterogeneity of whistling face or Freeman-Sheldon syndrome in a Chinese family.
Wang TR; Lin SJ
Am J Med Genet; 1987 Oct; 28(2):471-5. PubMed ID: 3425620
[TBL] [Abstract][Full Text] [Related]
5. Freeman-Sheldon syndrome: a case report.
Aren G; Yurdabakan Z; Ozcan I
Quintessence Int; 2003 Apr; 34(4):307-10. PubMed ID: 12731619
[TBL] [Abstract][Full Text] [Related]
6. A new surgical procedure for correction of lip deformity in cranio-carpo-tarsal dysplasia (whistling face syndrome).
Vaitiekaitis AS; Hornstein L; Neale HW
J Oral Surg; 1979 Sep; 37(9):669-72. PubMed ID: 288890
[TBL] [Abstract][Full Text] [Related]
7. New evidence for genetic heterogeneity of the Freeman-Sheldon syndrome.
Sánchez JM; Kaminker CP
Am J Med Genet; 1986 Nov; 25(3):507-11. PubMed ID: 3789012
[TBL] [Abstract][Full Text] [Related]
8. [A rare hand malformation, the Freeman-Sheldon syndrome].
Freilinger G; Rett A; Killian W
Handchirurgie; 1980; 12(3-4):225-7. PubMed ID: 7333533
[TBL] [Abstract][Full Text] [Related]
9. Autosomal recessive type of whistling face syndrome in twins.
Kousseff BG; McConnachie P; Hadro TA
Pediatrics; 1982 Mar; 69(3):328-31. PubMed ID: 7199706
[TBL] [Abstract][Full Text] [Related]
10. [The cranio-carpo-tarsal dysplasia syndrome (the Freeman-Sheldon whistling-face syndrome). Practical significance of diagnosis].
Kratzer W; Borm U
Monatsschr Kinderheilkd (1902); 1978 May; 126(5):277-9. PubMed ID: 418327
[No Abstract] [Full Text] [Related]
11. Freeman-Sheldon syndrome: report of one case.
Wu SC; Chang ML
Acta Paediatr Taiwan; 2005; 46(5):314-7. PubMed ID: 16640009
[TBL] [Abstract][Full Text] [Related]
12. [Cranio-carpo-tarsal dysplasia syndrome (Freeman-Sheldon syndrome, whistling face syndrome)].
Träger D
Z Orthop Ihre Grenzgeb; 1987; 125(1):106-7. PubMed ID: 3577337
[TBL] [Abstract][Full Text] [Related]
13. Report on two cases of Freeman-Sheldon syndrome ("whistling face).
Savini R; Gualdrini G
Ital J Orthop Traumatol; 1980 Apr; 6(1):105-15. PubMed ID: 7203992
[TBL] [Abstract][Full Text] [Related]
14. Freeman-Sheldon (whistling face) syndrome with hyperpyrexia in the newborn: case report.
Altunhan H; Annagür A; Ertuğrul S; Pekcan S; Ors R
Genet Couns; 2010; 21(3):347-51. PubMed ID: 20964128
[TBL] [Abstract][Full Text] [Related]
15. Freeman Sheldon syndrome with marked kyphoscoliosis at birth: a case report.
Naher BS; Hossain A; Islam ST; Ali MA
Mymensingh Med J; 2013 Jan; 22(1):206-9. PubMed ID: 23416834
[TBL] [Abstract][Full Text] [Related]
16. Freeman-Sheldon syndrome. A case report and review of the literature.
Ferrari D; Bettuzzi C; Donzelli O
Chir Organi Mov; 2008 Sep; 92(2):127-31. PubMed ID: 18677448
[TBL] [Abstract][Full Text] [Related]
17. [Anesthetic management of a patient with Freeman-Sheldon ("whistling face") syndrome].
Tateishi M; Imaizumi H; Namiki A; Katsuno M; Kawana S; Ujike Y
Masui; 1986 Jul; 35(7):1114-8. PubMed ID: 3773258
[No Abstract] [Full Text] [Related]
18. The whistling face syndrome or cranio-carpo-tarsal dysplasia.
Ishii Y; Takeda K; Yoshitake K; Ono T
Kyoto Daigaku Kokukagaku Kiyo; 1978; 18():47-52. PubMed ID: 291500
[No Abstract] [Full Text] [Related]
19. The syndrome of diaphragmatic hernia, abnormal face and distal limb anomalies (Fryns syndrome): report of two sibs with further delineation of this multiple congenital anomaly (MCA) syndrome.
Moerman P; Fryns JP; Vandenberghe K; Devlieger H; Lauweryns JM
Am J Med Genet; 1988 Dec; 31(4):805-14. PubMed ID: 3239572
[TBL] [Abstract][Full Text] [Related]
20. Limb reduction defects and renal dysplasia: confirmation of a new, apparently lethal, autosomal recessive MCA syndrome.
Schrander-Stumpel C; de Die-Smulders C; Fryns JP; da Costa J; Bouckaert P
Am J Med Genet; 1990 Sep; 37(1):133-5. PubMed ID: 2240030
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
