Further evidence for an imprinted gene for neonatal diabetes localised to chromosome 6q22-q23

Human Molecular Genetics

Volumn 5, Issue 8, 1996, Pages 1117-1121

  Temple, I Karen ^a   Gardner, Rebecca J ^b   Robinson, David O ^b   Kibirige, Mohammed S ^c   Ferguson, Arthur W ^d   Baum, J David ^e   Barber, John C K ^b   James, Rowena S ^b   Shield, Julian P H ^e  

^a PRINCESS ANNE HOSPITAL   (United Kingdom)

^b WESSEX REGIONAL GENETICS LABORATORY   (United Kingdom)

^c JAMES COOK UNIVERSITY HOSPITAL   (United Kingdom)

^d BEDFORD HOSPITAL   (United Kingdom)

^e UNIVERSITY OF BRISTOL   (United Kingdom)

Author keywords

[No Author keywords available]

Indexed keywords

ARTICLE; CHROMOSOME 6Q; DIABETES MELLITUS; GENE DUPLICATION; GENE EXPRESSION; GENETIC LINKAGE; GENETIC PREDISPOSITION; GENOME IMPRINTING; HUMAN; NEWBORN; NON INSULIN DEPENDENT DIABETES MELLITUS; ONSET AGE; PRIORITY JOURNAL;

EID: 0029794055     PISSN: 09646906     EISSN: None     Source Type: Journal    
DOI: 10.1093/hmg/5.8.1117     Document Type: Article

References (22)

1. von Muhlendahl, K.E. and Herkenhoff, H. (1995) Long-term course of neonatal diabetes. N. Engl. J. Med., 333, 704-708.
2. Milner, R.D.G., Ferguson, A.W. and Naidu, S.H. (1971) Aetiology of transient neonatal diabetes. Arch. Dis. Child., 46, 724-726.
3. Shield, J.P.M. and Baum, J.D. (1995) Transient neonatal diabetes and later onset diabetes: a case of inherited insulin resistance. Arch. Dis. Child., 72, 56-57.
4. Temple, I.K., James, R.S., Crolla, J.A., Sitch, F.L., Jacobs, P.A., Howell, W.M., Betts, P., Baum, J.D. and Shield, J.P.H. (1995) An imprinted gene(s) for diabetes? Nature Genet., 9, 110-112.
5. Pivnik, E.K., Qumsiyeh, M.B., Tharapel, A.T., Summitt, J.B. and Wilroy, R.S. (1990) Partial duplication of the long arm of chromosome 6: a clinically recognisable syndrome. J. Med. Genet., 27, 523-526.
6. Ziel, B., Zneimer, S.M. and Bachman, R. (1995) Partial trisomy of chromosome 6q, an interstitial duplication of the long arm. Am. J. Hum. Genet., 53, 4 (suppl) A131 Abstract 741.
7. Gyapay, G., Morisette, J., Vignal, A., Dib, C., Fizames, C., Millasseau, P., Marc, S., Bernadi, G., Lathrop, M. and Weissenbach, J. (1994) The 1993-94 Genethon human genetic linkage map. Nature Genet., 7, 246-339.
8. Morton, N.E., Collins, A., Lawrence, S. and Shields, D.C. (1992) Algorithms for a location database. Ann. Hum. Genet., 56, 223-232.
9. Ferguson, A.W. and Milner, R.D.G. (1970) Transient neonatal diabetes mellitus in sibs. Arch. Dis. Child., 45, 80-83.
10. Wilson, S. (1991) Transient neonatal diabetes. Nursing Times, 87, 44-45.
11. McGill, J.J. and Roberten, D.M. (1986) A new type of transient diabetes mellitus of infancy? Arch. Dis. Child., 61, 334-336.
12. Abramowicz, M.J., Andrien, M., Dupont, E., Dorchy, H., Parma, J., Duprez, L., Ledley, F.D., Courtens, W. and Vamos, E. (1994) Isodisomy of chromosome 6 in a newborn with methylmalonic acidaemia and agenesis of pancreatic beta cells causing diabetes mellitus. J. Clin. Invest., 94, 418-421.
13. Franchino, C.J., Beneck, D., Greco, M.A. and Wolman, S.R. (1987) Partial trisomy 6q: case report with necropsy findings. J. Med. Genet., 24, 300-312.
14. Chase, T.R., Jalal, S.M., Martsolf, J.T. and Wasdahl, W.A. (1983) Duplication 6q24-6qter in an infant from a balanced paternal translocation. Am. J. Med. Genet., 14, 347-351.
15. Pandya, A., Braverman, N., Pyeritz, R.E., Ying, K.-L., Kline, A.D. and Falk, R.E. (1995) Interstitial deletion of the long arm of chromosome 6 associated with unusual limb anomalies: report of two new patients and review of the literature. Am. J. Med. Genet., 59, 38-43.
16. Coffey, J.D. and Killelea, D.E. (1982) Transient neonatal diabetes in half sisters. A sequel. Am. J. Dis. Child., 136, 626-627.
17. Maddux, B.A., Sbraccia, P., Kumakura, S., Sasson, S., Youngren, J., Fisher, A., Spencer, S., Grupe, A., Henzel, W., Srewart, T.A., Reaven, G.M. and Goldfine, I.D. (1995) Membrane glycoprotein PC-1 and insulin resistance in non-insulin-dependent diabetes mellitus. Nature, 373, 448-451.
18. Buckley, M.F., Loveland, K.A., McKinstry, W.J., Garson, O.M. and Goding, J.W. (1990) Plasma cell membrane glycoprotein PC-1: cDNA cloning of the human molecule, amino acid sequence and chromosomal location. J. Biol. Chem., 265, 17506-17511.
19. Miller, S.A., Dykes, D.D. and Polesky, H.F. (1988) A simple salting out procedure for extracting DNA from human nucleated cells. Nucleic Acids Res., 16, 1215.
20. Hudson, T.J., Engelstein, M., Lee, M.K., Ho, B.C., Rubenfeld, M.J., Adams, C.P., Housman, D.E. and Dracopoli, N.C. (1992) Isolation and chromosome assignment of 100 highly informative human simple sequence repeat polymorphisms. Genomics, 13, 622-629.
21. Webber, L.M. and Garson, O.M. (1983) Fluorodeoxyuridine synchronization of bone marrow cultures. Cancer Genet. Cytogenet., 8, 123-132.
22. Pinkel, D., Landegent, J., Collins, C., Fuscoe, J., Segraves, R., Lucas, J. and Gray, J. (1988) Fluorescence in situ hybridisation with human chromosome-specific libraries: detection of trisomy 21 and translocations of chromosome 4. Proc. Natl Acad Sci. USA, 85, 9138-9142.