Works matching IS 03406717 AND DT 2003 AND VI 112 AND IP 3
Results: 18
Human genetic disease caused by de novo mitochondrial-nuclear DNA transfer.
- Published in:
- Human Genetics, 2003, v. 112, n. 3, p. 303, doi. 10.1007/s00439-002-0892-2
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- Publication type:
- Article
Acknowledgement to referees 2002.
- Published in:
- Human Genetics, 2003, v. 112, n. 3, p. 324, doi. 10.1007/s00439-003-0929-1
- Publication type:
- Article
Fragile X syndrome: diagnosis, treatment and research: Randi Jenssen Hagerman, Paul J Hagerman (eds) John Hopkins University Press, ISBN 0-8018-6843-2 (hardcover) £ 65.50; ISBN 0-8018-6844-0 (paperback) £ 31.00.
- Published in:
- 2003
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- Publication type:
- Book Review
Patterns of associations of clinical features in neurofibromatosis 1 (NF1).
- Published in:
- Human Genetics, 2003, v. 112, n. 3, p. 289, doi. 10.1007/s00439-002-0871-7
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- Article
Helen M. Kingston: ABC of Clinical Genetics (3rd edn): BJM Books, ISBN 0727916270, softcover, £17.95.
- Published in:
- 2003
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- Publication type:
- Book Review
The novel imprinted carboxypeptidase A4 gene (CPA4) in the 7q32 imprinting domain.
- Published in:
- Human Genetics, 2003, v. 112, n. 3, p. 220, doi. 10.1007/s00439-002-0891-3
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- Publication type:
- Article
Thank you Robert Nussbaum, Welcome Thomas Hudson!
- Published in:
- Human Genetics, 2003, v. 112, n. 3, p. 219, doi. 10.1007/s00439-003-0918-4
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- Publication type:
- Article
Founder effect of the C9 R95X mutation in Orientals.
- Published in:
- Human Genetics, 2003, v. 112, n. 3, p. 244, doi. 10.1007/s00439-002-0870-8
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- Publication type:
- Article
Relation of risk of systemic lupus erythematosus to west African admixture in a Caribbean population.
- Published in:
- Human Genetics, 2003, v. 112, n. 3, p. 310, doi. 10.1007/s00439-002-0883-3
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- Publication type:
- Article
Duplication of the MID1 first exon in a patient with Opitz G/BBB syndrome.
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- Human Genetics, 2003, v. 112, n. 3, p. 249, doi. 10.1007/s00439-002-0901-5
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- Publication type:
- Article
Frederick Burkhardt, Duncan M. Porter, Sheila Ann Dean, Jonathan R. Topham, Sarah Wilmot (eds): The Correspondence of Charles Darwin 1864 (Vol. 12): Cambridge University Press, ISBN 0521590345, £55.00, hardcover.
- Published in:
- 2003
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- Publication type:
- Book Review
Relevance of sequence and structure elements for deletion events in the dystrophin gene major hot-spot.
- Published in:
- Human Genetics, 2003, v. 112, n. 3, p. 272, doi. 10.1007/s00439-002-0881-5
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- Publication type:
- Article
Testing hypotheses of language replacement in the Caucasus: evidence from the Y-chromosome.
- Published in:
- Human Genetics, 2003, v. 112, n. 3, p. 255, doi. 10.1007/s00439-002-0874-4
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- Publication type:
- Article
A novel autosomal dominant non-syndromic deafness locus (DFNA48) maps to 12q13-q14 in a large Italian family.
- Published in:
- Human Genetics, 2003, v. 112, n. 3, p. 319, doi. 10.1007/s00439-002-0880-6
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- Publication type:
- Article
Assessment of the CTNNA3 gene encoding human αT-catenin regarding its involvement in dilated cardiomyopathy.
- Published in:
- Human Genetics, 2003, v. 112, n. 3, p. 227, doi. 10.1007/s00439-002-0857-5
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- Publication type:
- Article
Influence of interleukin-12 receptor β1 polymorphisms on tuberculosis.
- Published in:
- Human Genetics, 2003, v. 112, n. 3, p. 237, doi. 10.1007/s00439-002-0873-5
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- Publication type:
- Article
A study of cryptic terminal chromosome rearrangements in recurrent miscarriage couples detects unsuspected acrocentric pericentromeric abnormalities.
- Published in:
- Human Genetics, 2003, v. 112, n. 3, p. 298, doi. 10.1007/s00439-002-0887-z
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- Publication type:
- Article
FMR1 haplotype analyses among Indians: a weak founder effect and other findings.
- Published in:
- Human Genetics, 2003, v. 112, n. 3, p. 262, doi. 10.1007/s00439-002-0872-6
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- Publication type:
- Article