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Pubmed for Handhelds
PUBMED FOR HANDHELDS
Journal Abstract Search
128 related items for PubMed ID: 12072805
1. Cenani-Lenz syndrome: report of a new case and review of the literature. Nezarati MM, McLeod DR. Clin Dysmorphol; 2002 Jul; 11(3):215-8. PubMed ID: 12072805 [Abstract] [Full Text] [Related]
2. Cooks syndrome: a case report and brief review. Brennan CB, Buehler T, Lesher JL. Pediatr Dermatol; 2013 Jul; 30(4):e52-3. PubMed ID: 22329539 [Abstract] [Full Text] [Related]
3. Keipert syndrome: two further cases and review of the literature. Nik-Zainal S, Holder SE, Cruwys M, Hall CM, Shaw-Smith C. Clin Dysmorphol; 2008 Jul; 17(3):169-175. PubMed ID: 18541962 [No Abstract] [Full Text] [Related]
4. A variant of Cenani-Lenz type syndactyly. Seven M, Yüksel A, Ozkiliç A, Elçioğlu N. Genet Couns; 2000 Jul; 11(1):41-7. PubMed ID: 10756427 [Abstract] [Full Text] [Related]
5. Hands and feet in the Apert syndrome. Cohen MM, Kreiborg S. Am J Med Genet; 1995 May 22; 57(1):82-96. PubMed ID: 7645606 [Abstract] [Full Text] [Related]
6. Unusual combination of limb malformations in the same patient: brachydactyly with syndactyly and postaxial polydactyly of the hands and postaxial oligodactyly of the feet. Ferda Percin E, Yilmaz S. Clin Dysmorphol; 2003 Oct 22; 12(4):283-4. PubMed ID: 14564221 [Abstract] [Full Text] [Related]
7. [Type II dentin dysplasia combined with a skeletal anomaly]. Beliakov IuA, Bogdashevskaia VB, Blokhina MI, Ovechkina AA. Stomatologiia (Mosk); 1988 Oct 22; 67(3):67-9. PubMed ID: 3166257 [No Abstract] [Full Text] [Related]
8. Two isolated cases with symmetrically absent hands and feet. Horn D, Kolb GP. Clin Dysmorphol; 1994 Jul 22; 3(3):228-33. PubMed ID: 7981858 [Abstract] [Full Text] [Related]
9. Catel-Manzke syndrome without cleft palate: a case report. Puri RD, Phadke SR. Clin Dysmorphol; 2003 Oct 22; 12(4):279-81. PubMed ID: 14564220 [Abstract] [Full Text] [Related]
10. RSH (Smith-Lemli-Opitz) syndrome: "severe" phenotype with ectrodactyly. de Jong G, Kirby PA, Muller LM. Am J Med Genet; 1998 Jan 23; 75(3):283-7. PubMed ID: 9475598 [Abstract] [Full Text] [Related]
11. Fibular aplasia, tibial campomelia, and oligosyndactyly: a further patient with a 2-year follow-up. Sezer O, Gebesoglu I, Yuan B, Karaca E, Gokce E, Gunes S. Clin Dysmorphol; 2014 Oct 23; 23(4):121-6. PubMed ID: 25144151 [No Abstract] [Full Text] [Related]
12. Probable identity of Goltz syndrome and Van Allen-Myhre syndrome: evidence from phenotypic evolution. Hancock S, Pryde P, Fong C, Brazy JE, Stewart K, Favour A, Pauli RM. Am J Med Genet; 2002 Jul 15; 110(4):370-9. PubMed ID: 12116212 [Abstract] [Full Text] [Related]
14. Raine syndrome: report of a case with hand and foot anomalies. Mahafza T, El-Shanti H, Omari H. Clin Dysmorphol; 2001 Jul 15; 10(3):227-9. PubMed ID: 11446420 [No Abstract] [Full Text] [Related]
16. Severe manifestations of hand-foot-genital syndrome associated with a novel HOXA13 mutation. Imagawa E, Kayserili H, Nishimura G, Nakashima M, Tsurusaki Y, Saitsu H, Ikegawa S, Matsumoto N, Miyake N. Am J Med Genet A; 2014 Sep 15; 164A(9):2398-402. PubMed ID: 24934387 [Abstract] [Full Text] [Related]
17. A novel type of autosomal recessive syndactyly: clinical and molecular studies in a family of Pakistani origin. Malik S, Arshad M, Amin-Ud-Din M, Oeffner F, Dempfle A, Haque S, Koch MC, Ahmad W, Grzeschik KH. Am J Med Genet A; 2004 Apr 01; 126A(1):61-7. PubMed ID: 15039974 [Abstract] [Full Text] [Related]
19. A lobster claw abnormality in the common marmoset (Callithrix jacchus). Cooper JE, Purton P, Poswillo DE. Lab Anim; 1990 Apr 01; 24(2):151-5. PubMed ID: 2366513 [Abstract] [Full Text] [Related]
20. Catel-Manzke digitopalatal syndrome or Temtamy preaxial brachydactyly hyperphalangism syndrome? Temtamy SA. Clin Dysmorphol; 2005 Oct 01; 14(4):211. PubMed ID: 16155426 [No Abstract] [Full Text] [Related] Page: [Next] [New Search]