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4. A variant form of Laurin-Sandrow syndrome in an adult patient. Buzea C; Panazan T; Boiangiu I J Hand Surg Eur Vol; 2020 Mar; 45(3):306-308. PubMed ID: 31813304 [No Abstract] [Full Text] [Related]
5. [Prevalence of congenital split hand/split foot malformation in Chinese population]. Dai L; Li YH; Deng Y; Zhu J; Wang YP; Liang J; Zhang YW; Liu ZY Sichuan Da Xue Xue Bao Yi Xue Ban; 2010 Mar; 41(2):320-3. PubMed ID: 20506663 [TBL] [Abstract][Full Text] [Related]
6. Mirror hands and feet with a distinct nasal defect, an autosomal dominant condition. Martin RA; Jones MC; Jones KL Am J Med Genet; 1993 Apr; 46(2):129-31. PubMed ID: 8387244 [No Abstract] [Full Text] [Related]
7. Early Surgical Correction of the Nasal Deformity in Laurin-Sandrow Syndrome. Roman P; Lypka M J Craniofac Surg; 2017 Mar; 28(2):e126-e127. PubMed ID: 28234639 [TBL] [Abstract][Full Text] [Related]
8. Acheiropody. A report of two cases. Kruger LM; Kumar A J Bone Joint Surg Am; 1994 Oct; 76(10):1557-60. PubMed ID: 7929505 [No Abstract] [Full Text] [Related]
9. Laurin-Sandrow Syndrome: A Case Report and Review of Literature. Sathishkumar K; Anand S J Hand Surg Asian Pac Vol; 2022 Aug; 27(4):742-746. PubMed ID: 35965362 [TBL] [Abstract][Full Text] [Related]
10. "Laurin-Sandrow Syndrome - a review of the literature and classification system". Buzea C; Boulanger N Clin Dysmorphol; 2022 Jul; 31(3):109-112. PubMed ID: 35256564 [TBL] [Abstract][Full Text] [Related]
11. Laurin-Sandrow syndrome (mirror hands and feet and nasal defects): description of a new case. Martínez-Frías ML; Alcaraz M; Espejo P; Gómez MA; García de León R; González Moro L J Med Genet; 1994 May; 31(5):410-2. PubMed ID: 8064822 [TBL] [Abstract][Full Text] [Related]
12. Amniotic band sequence and limb defects: data from a population-based study. Froster UG; Baird PA Am J Med Genet; 1993 Jun; 46(5):497-500. PubMed ID: 8322808 [TBL] [Abstract][Full Text] [Related]
13. Intrafamilial variability of ZRS-associated syndrome: characterization of a mosaic ZRS mutation by pyrosequencing. Vanlerberghe C; Faivre L; Petit F; Fruchart O; Jourdain AS; Clavier F; Gay S; Manouvrier-Hanu S; Escande F Clin Genet; 2015 Nov; 88(5):479-83. PubMed ID: 25382487 [TBL] [Abstract][Full Text] [Related]
14. Male-to-male transmission in Laurin-Sandrow syndrome and exclusion of RARB and RARG. Kjaer KW; Hansen L; Eiberg H; Christensen KS; Opitz JM; Tommerup N Am J Med Genet A; 2005 Aug; 137(2):148-52. PubMed ID: 16059937 [TBL] [Abstract][Full Text] [Related]
15. Sandrow syndrome of mirror hands and feet and facial abnormalities. Kogekar N; Teebi AS; Vockley J Am J Med Genet; 1993 Apr; 46(2):126-8. PubMed ID: 8387243 [TBL] [Abstract][Full Text] [Related]
16. Laurin-Sandrow syndrome: review and redefinition. Mariño-Enríquez A; Lapunzina P; Omeñaca F; Morales C; Rodríguez JI Am J Med Genet A; 2008 Oct; 146A(19):2557-65. PubMed ID: 18792985 [TBL] [Abstract][Full Text] [Related]
17. B cell immunodeficiency, distal limb abnormalities, and urogenital malformations in a three generation family: a novel autosomal dominant syndrome? Edery P; Le Deist F; Briard ML; Debré M; Munnich A; Griscelli C; Fischer A; Lyonnet S J Med Genet; 2001 Jul; 38(7):488-93. PubMed ID: 11476068 [No Abstract] [Full Text] [Related]
18. The hand-foot-genital syndrome: on the variable expression in affected males. Fryns JP; Vogels A; Decock P; van den Berghe H Clin Genet; 1993 May; 43(5):232-4. PubMed ID: 8375102 [TBL] [Abstract][Full Text] [Related]
19. Autosomal dominant tibial hemimelia-polysyndactyly-triphalangeal thumbs syndrome: report of a Brazilian family. Richieri-Costa A; de Miranda E; Kamiya TY; Freire-Maia DV Am J Med Genet; 1990 May; 36(1):1-6. PubMed ID: 2333896 [TBL] [Abstract][Full Text] [Related]
20. [Split hand/foot abnormalities: classification, pathogenesis, epidemiology]. Elek C; Vitéz M; Czeizel E Orv Hetil; 1991 Jul; 132(30):1639-42. PubMed ID: 1866158 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]