Literature DB >> 8104766

Report and abstracts of the Fourth International Workshop on Human Chromosome 3 Mapping.

S L Naylor1, C H Buys, B Carritt.   

Abstract

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Year:  1994        PMID： 8104766

Source DB:  PubMed          Journal:  Cytogenet Cell Genet        ISSN： 0301-0171


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  11 in total

1.  Precise localisation of 3p25 breakpoints in four patients with the 3p-syndrome.

Authors:  T Drumheller; B C McGillivray; D Behrner; P MacLeod; D E McFadden; J Roberson; C Venditti; K Chorney; M Chorney; D I Smith
Journal:  J Med Genet       Date:  1996-10       Impact factor: 6.318

2.  Gestational drive and the green-bearded placenta.

Authors:  D Haig
Journal:  Proc Natl Acad Sci U S A       Date:  1996-06-25       Impact factor: 11.205

3.  Losses at 3p common deletion sites in subtypes of kidney tumours: histopathological correlations.

Authors:  P Hadaczek; J Podolski; A Toloczko; G Kurzawski; A Sikorski; P Rabbitts; K Huebner; J Lubinski
Journal:  Virchows Arch       Date:  1996-09       Impact factor: 4.064

4.  Mapping the Bst mutation on mouse chromosome 16: a model for human optic atrophy.

Authors:  D S Rice; R W Williams; P Ward-Bailey; K R Johnson; B S Harris; M T Davisson; D Goldowitz
Journal:  Mamm Genome       Date:  1995-08       Impact factor: 2.957

5.  Tuberous sclerosis-associated renal cell carcinoma. Clinical, pathological, and genetic features.

Authors:  J Bjornsson; M P Short; D J Kwiatkowski; E P Henske
Journal:  Am J Pathol       Date:  1996-10       Impact factor: 4.307

6.  Allelic loss is frequent in tuberous sclerosis kidney lesions but rare in brain lesions.

Authors:  E P Henske; B W Scheithauer; M P Short; R Wollmann; J Nahmias; N Hornigold; M van Slegtenhorst; C T Welsh; D J Kwiatkowski
Journal:  Am J Hum Genet       Date:  1996-08       Impact factor: 11.025

7.  Chromosome 3p loss of heterozygosity and mutation analysis of the FHIT and beta-cat genes in squamous cell carcinoma of the head and neck.

Authors:  M V González; M F Pello; P Ablanedo; C Suárez; V Alvarez; E Coto
Journal:  J Clin Pathol       Date:  1998-07       Impact factor: 3.411

8.  Insertion of an Alu sequence in the Ca(2+)-sensing receptor gene in familial hypocalciuric hypercalcemia and neonatal severe hyperparathyroidism.

Authors:  N Janicic; Z Pausova; D E Cole; G N Hendy
Journal:  Am J Hum Genet       Date:  1995-04       Impact factor: 11.025

9.  Sublocalization of a locus at 3p21.3-23 predisposing to hereditary nonpolyposis colon cancer.

Authors:  P Tannergård; E Zabarovsky; E Stanbridge; M Nordenskjöld; A Lindblom
Journal:  Hum Genet       Date:  1994-08       Impact factor: 4.132

10.  Close linkage to chromosome 3p and conservation of ancestral founding haplotype in hereditary nonpolyposis colorectal cancer families.

Authors:  M Nyström-Lahti; P Sistonen; J P Mecklin; L Pylkkänen; L A Aaltonen; H Järvinen; J Weissenbach; A de la Chapelle; P Peltomäki
Journal:  Proc Natl Acad Sci U S A       Date:  1994-06-21       Impact factor: 11.205
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