148 related articles for article (PubMed ID: 6674411)
21. Congenital contractures, ectodermal dysplasia, cleft lip/palate, and developmental impairment: a distinct syndrome.
Ladda RL; Zonana J; Ramer JC; Mascari MJ; Rogan PK
Am J Med Genet; 1993 Sep; 47(4):550-5. PubMed ID: 7504881
[TBL] [Abstract][Full Text] [Related]
22. [Anatomy of the nasal cartilages of the unilateral lip and palate cleft nose].
Li A; Sun Y; Zhang K
Zhonghua Kou Qiang Yi Xue Za Zhi; 1997 May; 32(3):167-8. PubMed ID: 10680530
[TBL] [Abstract][Full Text] [Related]
23. [Consequences of early diagnosis of congenital abnormalities].
Passarge E; Mecke S
Munch Med Wochenschr; 1971 May; 113(22):853-5. PubMed ID: 5108536
[No Abstract] [Full Text] [Related]
24. Craniofrontonasal dysplasia in two male sibs.
Natarajan U; Baraitser M; Nicolaides K; Gosden C
Clin Dysmorphol; 1993 Oct; 2(4):360-4. PubMed ID: 8305967
[TBL] [Abstract][Full Text] [Related]
25. New autosomal dominant syndrome resembling craniofrontonasal dysplasia.
Teebi AS
Am J Med Genet; 1987 Nov; 28(3):581-91. PubMed ID: 3425628
[TBL] [Abstract][Full Text] [Related]
26. [Familial split hand and foot, cleft lip and palate, ectodermal dysplasia syndrome].
Szappanos L; Czeizel E; Szepesi K
Orv Hetil; 1984 Mar; 125(11):633-8. PubMed ID: 6700970
[No Abstract] [Full Text] [Related]
27. Agenesis of the corpus callosum, combined immunodeficiency, bilateral cataract, and hypopigmentation in two brothers.
Dionisi Vici C; Sabetta G; Gambarara M; Vigevano F; Bertini E; Boldrini R; Parisi SG; Quinti I; Aiuti F; Fiorilli M
Am J Med Genet; 1988 Jan; 29(1):1-8. PubMed ID: 3344762
[TBL] [Abstract][Full Text] [Related]
28. 4p- syndrome and 9p tetrasomy mosaicism with cleft lip and palate.
Kobayashi J; Kimijima Y; Yamada S; Amagasa T; Saito-Ohara F
J Craniomaxillofac Surg; 2000 Jun; 28(3):165-70. PubMed ID: 10964553
[TBL] [Abstract][Full Text] [Related]
29. Case of polyhydramnios complicated by Opitz G/BBB syndrome.
Tajima H; Itoh H; Mochizuki A; Nakamura Y; Kobayashi Y; Hirai K; Suzuki K; Sugihara K; Ohishi A; Ohzeki T; Kanayama N
J Obstet Gynaecol Res; 2010 Aug; 36(4):876-81. PubMed ID: 20666962
[TBL] [Abstract][Full Text] [Related]
30. Frontonasal dysplasia with corpus callosum lipoma.
Grover SB; Charan KA; Saxena NC
Indian Pediatr; 1999 Apr; 36(4):398-401. PubMed ID: 10717702
[No Abstract] [Full Text] [Related]
31. Phenotypic variability of Pai syndrome: report of two patients and review of the literature.
Vaccarella F; Pini Prato A; Fasciolo A; Pisano M; Carlini C; Seymandi PL
Int J Oral Maxillofac Surg; 2008 Nov; 37(11):1059-64. PubMed ID: 18657395
[TBL] [Abstract][Full Text] [Related]
32. Limb pterygium syndromes: a review and report of eleven patients.
Hall JG; Reed SD; Rosenbaum KN; Gershanik J; Chen H; Wilson KM
Am J Med Genet; 1982 Aug; 12(4):377-409. PubMed ID: 7124793
[TBL] [Abstract][Full Text] [Related]
33. Open tip rhinoplasty along with the repair of cleft lip in cleft lip and palate cases.
Thomas C; Mishra P
Br J Plast Surg; 2000 Jan; 53(1):1-6. PubMed ID: 10657441
[TBL] [Abstract][Full Text] [Related]
34. Dominant inheritance of bifid nose.
Anyane-Yeboa K; Raifman MA; Berant M; Frogel MP; Travers H
Am J Med Genet; 1984 Mar; 17(3):561-3. PubMed ID: 6711607
[TBL] [Abstract][Full Text] [Related]
35. [Morning glory disc anomaly und frontonasal dysplasia].
Papageorgiou E; Schiefer U; Warmuth-Metz M; Weckerle P
Ophthalmologe; 2007 Aug; 104(8):709-12. PubMed ID: 17440733
[TBL] [Abstract][Full Text] [Related]
36. Peters'-Plus syndrome with agenesis of the corpus callosum: report of a case and confirmation of autosomal recessive inheritance.
Camera G; Centa A; Pozzolo S; Camera A
Clin Dysmorphol; 1993 Oct; 2(4):317-21. PubMed ID: 8305962
[TBL] [Abstract][Full Text] [Related]
37. Anorectal anomalies, diaphragmatic defect, cleft palate, lower lip pits, hypopigmentation and hypogammaglobulinemia A in Kabuki syndrome: a rare combination.
Abdel-Salam GM; Afifi HH; Eid MM; el-Badry TH; Kholoussi NM
Genet Couns; 2008; 19(3):309-17. PubMed ID: 18990987
[TBL] [Abstract][Full Text] [Related]
38. Syndromal frontonasal dysostosis in a child with a complex translocation involving chromosomes 3, 7, and 11.
Stevens CA; Qumsiyeh MB
Am J Med Genet; 1995 Feb; 55(4):494-7. PubMed ID: 7762593
[TBL] [Abstract][Full Text] [Related]
39. Sporadic congenital malformations of newborn inbred mice.
Kalter H
Teratology; 1968 May; 1(2):193-9. PubMed ID: 5759135
[No Abstract] [Full Text] [Related]
40. Holoprosencephaly anomaly with nasal and premaxillar agenesis (possibly autosomal recessive type).
Durmuş Aydoğdu S; Yakut A; Oner U; Akşit MA; Tel N
Turk J Pediatr; 1994; 36(2):157-62. PubMed ID: 8016918
[TBL] [Abstract][Full Text] [Related]
[Previous] [Next] [New Search]