260 related articles for article (PubMed ID: 4220007)
1. 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]
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. 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]
4. Median facial cleft syndrome in half-sisters. Dilemmas in genetic counseling.
Warkany J; Bofinger MK; Benton C
Teratology; 1973 Dec; 8(3):273-85. PubMed ID: 4767905
[No Abstract] [Full Text] [Related]
5. [The Freeman-Sheldon syndrome].
Grasshoff H; St Braun H; Sakreida M
Beitr Orthop Traumatol; 1978 May; 25(5):241-7. PubMed ID: 98163
[No Abstract] [Full Text] [Related]
6. [Cranio-carpo-tarsal dysplasia or the whistling face syndrome (author's transl)].
de la Peña J; de Torres ; Bonastre García F; Serrano JL; Crespo Valero C
An Esp Pediatr; 1974; 7(5):452-7. PubMed ID: 4218458
[No Abstract] [Full Text] [Related]
7. Acromelic frontonasal dysostosis.
Slaney SF; Goodman FR; Eilers-Walsman BL; Hall BD; Williams DK; Young ID; Hayward RD; Jones BM; Christianson AL; Winter RM
Am J Med Genet; 1999 Mar; 83(2):109-16. PubMed ID: 10190481
[TBL] [Abstract][Full Text] [Related]
8. Acro-fronto-facio-nasal dysostosis: report of a new Brazilian family.
Richieri-Costa A; Guion-Almeida ML; Pagnan NA
Am J Med Genet; 1992 Dec; 44(6):800-2. PubMed ID: 1481850
[TBL] [Abstract][Full Text] [Related]
9. O--short stature with abnormalities of the cranium and limbs.
Jorgenson RJ
Birth Defects Orig Artic Ser; 1974; 10(5):249-51. PubMed ID: 4469995
[No Abstract] [Full Text] [Related]
10. The cloverleaf skull syndrome. Histological, histochemical and ultrastructural findings.
Bonucci E; Nardi F
Virchows Arch A Pathol Pathol Anat; 1972; 357(3):199-212. PubMed ID: 4628838
[No Abstract] [Full Text] [Related]
11. Craniocarpotarsal dystrophy--two case reports.
Georgiev E; Tzantcheva M
Acta Chir Plast; 1985; 27(3):152-9. PubMed ID: 3933233
[No Abstract] [Full Text] [Related]
12. Cryptophthalmos, dyscephaly, syndactyly and renal aplasia. Report of a case.
Varnek L
Acta Ophthalmol (Copenh); 1978 Apr; 56(2):302-13. PubMed ID: 208347
[TBL] [Abstract][Full Text] [Related]
13. Symphalangism and brachydactyly syndrome: report of the WL symphalangism-brachydactyly syndrome: review of literature and classification.
Herrmann J
Birth Defects Orig Artic Ser; 1974; 10(5):23-53. PubMed ID: 4469994
[No Abstract] [Full Text] [Related]
14. [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]
15. [Associated malformations of the head and extremities].
Tridon P
J Genet Hum; 1974 Dec; 22(4):365-80. PubMed ID: 4282383
[No Abstract] [Full Text] [Related]
16. Genetics of the Meckel syndrome (dysencephalia splanchnocystica).
Hsia YE; Bratu M; Herbordt A
Pediatrics; 1971 Aug; 48(2):237-47. PubMed ID: 4997860
[No Abstract] [Full Text] [Related]
17. Craniofacial dysplasia with features of the midface syndrome.
Jorgenson RJ
Birth Defects Orig Artic Ser; 1971 Jun; 7(7):307. PubMed ID: 5173756
[No Abstract] [Full Text] [Related]
18. The VSR syndrome. Studies of malformation syndromes of man XXXII.
Herrmann J; Opitz JM
Birth Defects Orig Artic Ser; 1974; 10(9):227-39. PubMed ID: 4425539
[No Abstract] [Full Text] [Related]
19. Otopalatodigital syndrome type II.
Holder SE; Winter RM
J Med Genet; 1993 Apr; 30(4):310-3. PubMed ID: 8487277
[No Abstract] [Full Text] [Related]
20. Trisomy 18 with karyotype 47,XX,-18,+i psu dic(18p).
Romain DR; Dagger P; Columbano-Green LM; Smythe RH; Parfitt RG
J Med Genet; 1992 Jul; 29(7):513. PubMed ID: 1640437
[No Abstract] [Full Text] [Related]
[Next] [New Search]
