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24. 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]
25. [Transient neonatal hypocalcemia. Onset Manifestation of the 22q11.2 deletion syndrome]. Pusceddu M; Bertone A; Campra D; Pontoriero D; Guala A Minerva Pediatr; 2002 Aug; 54(4):343-5. PubMed ID: 12131871 [No Abstract] [Full Text] [Related]
30. [Methods of research on the chromosome level in diagnosing genetic disorders]. Ruffini E Minerva Pediatr; 1989 Sep; 41(9):491-2. PubMed ID: 2586382 [No Abstract] [Full Text] [Related]
31. Ascertainment of genetic disease in relatives of affected persons. McKusick VA Isr J Med Sci; 1973; 9(9):1358-60. PubMed ID: 4775118 [No Abstract] [Full Text] [Related]
32. [Use of DNA polymorphism in the diagnosis of human genetic diseases]. Cebrat S Postepy Hig Med Dosw; 1988; 42(5):461-82. PubMed ID: 2908211 [No Abstract] [Full Text] [Related]
33. "Genetic for medical practitioners". Ambani LM Q Med Rev; 1981 Oct; 32(4):1-43. PubMed ID: 7051087 [No Abstract] [Full Text] [Related]
34. Dual-probe fluorescence in situ hybridization assay for detecting deletions associated with VCFS/DiGeorge syndrome I and DiGeorge syndrome II loci. Berend SA; Spikes AS; Kashork CD; Wu JM; Daw SC; Scambler PJ; Shaffer LG Am J Med Genet; 2000 Apr; 91(4):313-7. PubMed ID: 10766989 [TBL] [Abstract][Full Text] [Related]
35. First-trimester screening for chromosomal abnormalities: advantages of an instant results approach. Norton ME Clin Lab Med; 2010 Sep; 30(3):565-71. PubMed ID: 20638572 [TBL] [Abstract][Full Text] [Related]