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22. Microlissencephaly in microcephalic osteodysplastic primordial dwarfism: a case report and review of the literature. Klinge L; Schaper J; Wieczorek D; Voit T Neuropediatrics; 2002 Dec; 33(6):309-13. PubMed ID: 12571786 [TBL] [Abstract][Full Text] [Related]
23. A syndrome of microcephaly, mental retardation, unusual facies, cleft palate, and weight deficiency. Weaver DD; Williams CP Birth Defects Orig Artic Ser; 1977; 13(3B):69-84. PubMed ID: 890101 [TBL] [Abstract][Full Text] [Related]
24. Anesthesia for cleft lip surgery in a child with Seckel syndrome--a case report. Rajamani A; Kamat V; Murthy J; Hussain SA Paediatr Anaesth; 2005 Apr; 15(4):338-41. PubMed ID: 15787928 [TBL] [Abstract][Full Text] [Related]
25. [Seckel dwarfism based on a personal case]. Howanietz H; Frisch H; Jedlicka-Köhler I; Steger H Klin Padiatr; 1989; 201(2):139-41. PubMed ID: 2716236 [TBL] [Abstract][Full Text] [Related]
26. Striking hematological abnormalities in patients with microcephalic osteodysplastic primordial dwarfism type II (MOPD II): a potential role of pericentrin in hematopoiesis. Unal S; Alanay Y; Cetin M; Boduroglu K; Utine E; Cormier-Daire V; Huber C; Ozsurekci Y; Kilic E; Simsek Kiper OP; Gumruk F Pediatr Blood Cancer; 2014 Feb; 61(2):302-5. PubMed ID: 24106199 [TBL] [Abstract][Full Text] [Related]
27. X-linked mental retardation, microcephaly, and growth delay associated with hereditary bullous dystrophy macular type: report of a second family. Lungarotti MS; Martello C; Barboni G; Mezzetti D; Mariotti G; Calabro A Am J Med Genet; 1994 Jul; 51(4):598-601. PubMed ID: 7943046 [TBL] [Abstract][Full Text] [Related]
28. Two Japanese cases with microcephalic primordial dwarfism: classical Seckel syndrome and osteodysplastic primordial dwarfism type II. Sugio Y; Tsukahara M; Kajii T Jpn J Hum Genet; 1993 Jun; 38(2):209-17. PubMed ID: 8358044 [TBL] [Abstract][Full Text] [Related]
29. Filippi syndrome: report of three additional cases. Williams MS; Williams JL; Wargowski DS; Pauli RM; Pletcher BA Am J Med Genet; 1999 Nov; 87(2):128-33. PubMed ID: 10533026 [TBL] [Abstract][Full Text] [Related]
31. [Type II primordial microcephalic dwarfism. Report of a patient with completed growth]. Théau D; Maroteaux P Ann Pediatr (Paris); 1993 May; 40(5):323-8. PubMed ID: 8346886 [TBL] [Abstract][Full Text] [Related]
32. Clinical and genetic heterogeneity of Seckel syndrome. Faivre L; Le Merrer M; Lyonnet S; Plauchu H; Dagoneau N; Campos-Xavier AB; Attia-Sobol J; Verloes A; Munnich A; Cormier-Daire V Am J Med Genet; 2002 Nov; 112(4):379-83. PubMed ID: 12376940 [TBL] [Abstract][Full Text] [Related]
33. Brief clinical report: the Dubowitz syndrome in a teenager. Fryns JP; Fabry G; Willemyns F; Van Den Berghe H Am J Med Genet; 1979; 4(4):345-7. PubMed ID: 575467 [TBL] [Abstract][Full Text] [Related]
34. Interstitial deletion 2q33.3-q34 in a boy with a phenotype resembling the Seckel syndrome. Courtens W; Speleman F; Messiaen L; Bormans J; Van Roy N; Vamos E Am J Med Genet; 1997 Sep; 71(4):479-85. PubMed ID: 9286460 [TBL] [Abstract][Full Text] [Related]
35. A case of cleft lip and palate associated with Seckel syndrome. Murthy J; Seshadri KG; Ramanan PV; Rajamani A; Hussain A Cleft Palate Craniofac J; 2004 Mar; 41(2):202-5. PubMed ID: 14989682 [TBL] [Abstract][Full Text] [Related]
36. Osteodysplastic variant of primordial dwarfism. Shebib S; Hugosson C; Sakati N; Nyhan WL Am J Med Genet; 1991 Aug; 40(2):146-50. PubMed ID: 1897566 [TBL] [Abstract][Full Text] [Related]
37. The Dubowitz syndrome: the psychological status of ten cases at follow-up. Parrish JM; Wilroy RS Am J Med Genet; 1980; 6(1):3-8. PubMed ID: 7190357 [TBL] [Abstract][Full Text] [Related]
39. Clinical, molecular and histopathological features of short stature syndrome with novel CUL7 mutation in Yakuts: new population isolate in Asia. Maksimova N; Hara K; Miyashia A; Nikolaeva I; Shiga A; Nogovicina A; Sukhomyasova A; Argunov V; Shvedova A; Ikeuchi T; Nishizawa M; Kuwano R; Onodera O J Med Genet; 2007 Dec; 44(12):772-8. PubMed ID: 17675530 [TBL] [Abstract][Full Text] [Related]
40. The Neu-Laxova syndrome: comments on syndrome identification. Fitch N; Resch L; Rochon L Am J Med Genet; 1982 Dec; 13(4):445-52. PubMed ID: 6891564 [No Abstract] [Full Text] [Related] [Previous] [Next] [New Search]