242 related articles for article (PubMed ID: 8042668)
21. Adams-Oliver syndrome and isolated aplasia cutis congenita in two siblings.
Rajabian MH; Aghaei S
Dermatol Online J; 2006 Oct; 12(6):17. PubMed ID: 17083897
[TBL] [Abstract][Full Text] [Related]
22. A case of Adams-Oliver syndrome associated with acrania, microcephaly, hemiplegia, epilepsy, and mental retardation.
Caksen H; Kurtoğlu S
Acta Neurol Belg; 2000 Dec; 100(4):252-5. PubMed ID: 11233683
[TBL] [Abstract][Full Text] [Related]
23. Finlay-Marks syndrome: another sporadic case and additional manifestations.
Taniai H; Chen H; Ursin S
Pediatr Int; 2004 Jun; 46(3):353-5. PubMed ID: 15151556
[No Abstract] [Full Text] [Related]
24. Familial aplasia cutis congenita and coarctation of the aorta.
Dallapiccola B; Giannotti A; Marino B; Digilio C; Obregon G
Am J Med Genet; 1992 Jul; 43(4):762-3. PubMed ID: 1621771
[TBL] [Abstract][Full Text] [Related]
25. Hallux syndactyly--ulnar polydactyly--abnormal ear lobes: a new syndrome.
Goldberg MJ; Pashayan HM
Birth Defects Orig Artic Ser; 1976; 12(5):255-66. PubMed ID: 182299
[TBL] [Abstract][Full Text] [Related]
26. [Scalp-ear-nipple syndrome].
Sonoda T
Ryoikibetsu Shokogun Shirizu; 2001; (34 Pt 2):606-7. PubMed ID: 11528920
[No Abstract] [Full Text] [Related]
27. Molecular basis of the scalp-ear-nipple syndrome unraveled by the characterization of disease-causing KCTD1 mutants.
Smaldone G; Balasco N; Pirone L; Caruso D; Di Gaetano S; Pedone EM; Vitagliano L
Sci Rep; 2019 Jul; 9(1):10519. PubMed ID: 31324836
[TBL] [Abstract][Full Text] [Related]
28. Cutaneous scar at anterior hair line in mother and child with associated frontal bone defect in child.
Stratis JP; Ramer JC; Manders EK; Lehman RA; Ladda RL
Am J Med Genet; 1992 Sep; 44(2):197-9. PubMed ID: 1456291
[TBL] [Abstract][Full Text] [Related]
29. Extensive form of aplasia cutis congenita: a new syndrome?
Park MS; Hahn SH; Hong CH; Kim JS; Kim HS
J Med Genet; 1998 Jul; 35(7):609-11. PubMed ID: 9678709
[TBL] [Abstract][Full Text] [Related]
30. Congenital scalp skull defects with distal limb anomalies (Adams-Oliver syndrome--McKusick 10030): further suggestion of autosomal recessive inheritance.
Koiffmann CP; Wajntal A; Huyke BJ; Castro RM
Am J Med Genet; 1988 Feb; 29(2):263-8. PubMed ID: 3354597
[TBL] [Abstract][Full Text] [Related]
31. ADULT syndrome allelic to limb mammary syndrome (LMS)?
Propping P; Friedl W; Wienker TF; Uhlhaas S; Zerres K
Am J Med Genet; 2000 Jan; 90(2):179-82. PubMed ID: 10607963
[TBL] [Abstract][Full Text] [Related]
32. A previously undescribed ectodermal dysplasia of the tricho-odonto-onychial subgroup in a family.
Tsakalakos N; Jordaan FH; Taljaard JJ; Hough SF
Arch Dermatol; 1986 Sep; 122(9):1047-53. PubMed ID: 3740884
[TBL] [Abstract][Full Text] [Related]
33. "New" ectodermal dysplasia with mental retardation and syndactyly.
Ilyina HG; Amoashy DS; Grygory HA
Am J Med Genet; 1995 Sep; 58(4):345-7. PubMed ID: 8533843
[TBL] [Abstract][Full Text] [Related]
34. Sparse hair, short stature, hypoplastic thumbs, single upper central incisor and abnormal skin pigmentation: a possible "new" form of ectodermal dysplasia.
Winter RM; MacDermot KD; Hill FJ
Am J Med Genet; 1988 Jan; 29(1):209-16. PubMed ID: 3344769
[TBL] [Abstract][Full Text] [Related]
35. Aplasia cutis congenita: three cases with three different underlying etiologies.
Mihçi E; Erişir S; Taçoy S; Lüleci G; Alpsoy E; Oygür N
Turk J Pediatr; 2009; 51(5):510-4. PubMed ID: 20112612
[TBL] [Abstract][Full Text] [Related]
36. Aplasia cutis congenita.
Deeken JH; Caplan RM
Arch Dermatol; 1970 Oct; 102(4):386-9. PubMed ID: 5536130
[No Abstract] [Full Text] [Related]
37. Pili torti and onychodysplasia. Report of a previously undescribed hidrotic ectodermal dysplasia.
Calzavara-Pinton P; Carlino A; Benetti A; De Panfilis G
Dermatologica; 1991; 182(3):184-7. PubMed ID: 1879585
[TBL] [Abstract][Full Text] [Related]
38. Type III syndactyly and oculodentodigital dysplasia: a clinical spectrum.
Schrander-Stumpel CT; De Groot-Wijnands JB; De Die-Smulders C; Fryns JP
Genet Couns; 1993; 4(4):271-6. PubMed ID: 8110413
[TBL] [Abstract][Full Text] [Related]
39. Aplasia cutis congenita, polythelia, microcephaly, and developmental delay: a unique expression of polytopic field defect involving possible 'paradominant' inheritance?
Urbani CE
Am J Med Genet A; 2004 Mar; 125A(3):327-8. PubMed ID: 14994248
[No Abstract] [Full Text] [Related]
40. A distinct type of hidrotic ectodermal dysplasia.
Halal F; Setton N; Wang NS
Am J Med Genet; 1991 Mar; 38(4):552-6. PubMed ID: 2063897
[TBL] [Abstract][Full Text] [Related]
[Previous] [Next] [New Search]