These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.
101 related articles for article (PubMed ID: 7606317)
21. Terminal deletion of the short arm of chromosome 3. Lizcano-Gil LA; Figuera LE Genet Couns; 1994; 5(1):35-8. PubMed ID: 8031533 [TBL] [Abstract][Full Text] [Related]
22. Annotation: behavioural phenotypes: a window onto the biology of behaviour. Flint J J Child Psychol Psychiatry; 1996 May; 37(4):355-67. PubMed ID: 8735436 [TBL] [Abstract][Full Text] [Related]
23. Natural history of the recombinant (8) syndrome. Sujansky E; Smith AC; Prescott KE; Freehauf CL; Clericuzio C; Robinson A Am J Med Genet; 1993 Sep; 47(4):512-25. PubMed ID: 8256815 [TBL] [Abstract][Full Text] [Related]
27. Wiedemann-Beckwith syndrome and chromosomal duplication 4q/deficiency 18p. Fryns JP; Kleczkowska A; Devriendt K; Devliegher H; Van den Berghe H Genet Couns; 1993; 4(1):37-41. PubMed ID: 8471219 [TBL] [Abstract][Full Text] [Related]
28. [Smith-Magenis syndrome: a case report]. Quijano Roy S; Delicado Navarro A; López Pajares I; Pascual-Castroviejo I An Esp Pediatr; 1998 Oct; 49(4):405-8. PubMed ID: 9859558 [No Abstract] [Full Text] [Related]
29. [Williams syndrome without cardiovascular abnormalities]. Cincinnati P; Genuardi M; Rutiloni C Minerva Pediatr; 1998 Nov; 50(11):467-71. PubMed ID: 10207296 [TBL] [Abstract][Full Text] [Related]
30. Partial duplication of 4q12q13 leads to a mild phenotype. Shashi V; Berry MN; Santos C; Pettenati MJ Am J Med Genet; 1999 Sep; 86(1):51-3. PubMed ID: 10440828 [TBL] [Abstract][Full Text] [Related]
31. Pallister-Killian syndrome: a mild case diagnosed by fluorescence in situ hybridization. Review of the literature and expansion of the phenotype. Bielanska MM; Khalifa MM; Duncan AM Am J Med Genet; 1996 Oct; 65(2):104-8. PubMed ID: 8911599 [TBL] [Abstract][Full Text] [Related]
32. Autosomal recessive mode of inheritance of a Coffin-Siris like syndrome. Bonioli E; Palmieri A; Bertola A; Bellini C Genet Couns; 1995; 6(4):309-12. PubMed ID: 8775417 [TBL] [Abstract][Full Text] [Related]
33. [Fragile X syndrome and mental retardation]. Estévez-González A; Roig C; Piles S; Pineda M; García-Sánchez C Rev Neurol; 1997 Jul; 25(143):1068-71. PubMed ID: 9280636 [TBL] [Abstract][Full Text] [Related]
34. Interstitial deletion of distal chromosome 4p in a patient without classical Wolf-Hirschhorn syndrome. Estabrooks LL; Rao KW; Korf B Am J Med Genet; 1993 Jan; 45(1):97-100. PubMed ID: 8418669 [TBL] [Abstract][Full Text] [Related]
35. A MELAS phenotype and a paternal inherited inversion of chromosome 10 in a female patient. Lorda-Sanchez I; Garcia-Ruiz PJ; Rodriguez de Alba M; Montoya J; Playan A; Sarasa JL; Trujillo MJ; Sanz R; Ramos C; Ayuso C Genet Couns; 2000; 11(3):261-5. PubMed ID: 11043434 [TBL] [Abstract][Full Text] [Related]
36. Is the autosomal dominant Optiz GBBB syndrome part of the DiGeorge/velocardiofacial syndrome with deletions of chromosome area 22q11.2? Wulfsberg EA Am J Med Genet; 1996 Aug; 64(3):523-4. PubMed ID: 8862634 [No Abstract] [Full Text] [Related]
37. Autosomal dominant "Opitz" GBBB syndrome due to a 22q11.2 deletion. McDonald-McGinn DM; Emanuel BS; Zackai EH Am J Med Genet; 1996 Aug; 64(3):525-6. PubMed ID: 8862635 [No Abstract] [Full Text] [Related]
38. Human haploinsufficiency--one for sorrow, two for joy. Fisher E; Scambler P Nat Genet; 1994 May; 7(1):5-7. PubMed ID: 8075640 [No Abstract] [Full Text] [Related]
39. Phenotype and counseling in lacrimo-auriculo-dento-digital (LADD) syndrome. Horn D; Witkowski R Genet Couns; 1993; 4(4):305-9. PubMed ID: 8110420 [TBL] [Abstract][Full Text] [Related]
40. Mosaicism for del(17)(p11.2p11.2) underlying the Smith-Magenis syndrome. Juyal RC; Kuwano A; Kondo I; Zara F; Baldini A; Patel PI Am J Med Genet; 1996 Dec; 66(2):193-6. PubMed ID: 8958329 [TBL] [Abstract][Full Text] [Related] [Previous] [Next] [New Search]