Literature DB >> 2676386

Report of the DNA committee and catalogs of cloned and mapped genes and DNA polymorphisms.

K K Kidd, A M Bowcock, J Schmidtke, R K Track, F Ricciuti, G Hutchings, A Bale, P Pearson, H F Willard, J Gelernter.   

Abstract

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Year:  1989        PMID： 2676386     DOI： 10.1159/000132810

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


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  77 in total

1.  An MspI polymorphism at the DXS11 locus.

Authors:  R Newton; S Forbes; G E Moore
Journal:  Nucleic Acids Res       Date:  1992-03-11       Impact factor: 16.971

2.  Molecular studies of parental origin and mosaicism in 45,X conceptuses.

Authors:  T Hassold; D Pettay; A Robinson; I Uchida
Journal:  Hum Genet       Date:  1992-08       Impact factor: 4.132

3.  Assignment of the gene for central core disease to chromosome 19.

Authors:  E A Haan; C J Freemantle; J A McCure; K L Friend; J C Mulley
Journal:  Hum Genet       Date:  1990-12       Impact factor: 4.132

4.  A comprehensive list of cloned human DNA sequences--1990 update.

Authors:  J Schmidtke; D N Cooper
Journal:  Nucleic Acids Res       Date:  1991-04-25       Impact factor: 16.971

5.  Molecular studies of non-disjunction in trisomy 16.

Authors:  T J Hassold; D Pettay; S B Freeman; M Grantham; N Takaesu
Journal:  J Med Genet       Date:  1991-03       Impact factor: 6.318

6.  Analysis of the origin of Turner's syndrome using polymorphic DNA probes.

Authors:  S A Loughlin; A Redha; J McIver; E Boyd; A Carothers; J M Connor
Journal:  J Med Genet       Date:  1991-03       Impact factor: 6.318

7.  Linkage studies in familial Alzheimer disease: evidence for chromosome 19 linkage.

Authors:  M A Pericak-Vance; J L Bebout; P C Gaskell; L H Yamaoka; W Y Hung; M J Alberts; A P Walker; R J Bartlett; C A Haynes; K A Welsh
Journal:  Am J Hum Genet       Date:  1991-06       Impact factor: 11.025

8.  Dystonia-parkinsonism syndrome (XDP) locus: flanking markers in Xq12-q21.1.

Authors:  K G Kupke; M B Graeber; U Müller
Journal:  Am J Hum Genet       Date:  1992-04       Impact factor: 11.025

9.  Genetic screening to identify the gene carrier in Italian and German kindreds affected by multiple endocrine neoplasia type 1 (MEN 1) syndrome.

Authors:  A Morelli; A Falchetti; R Castello; L Furlani; P Tomassetti; F Tonelli; A Frilling; M Serio; M L Brandi
Journal:  J Endocrinol Invest       Date:  1995-05       Impact factor: 4.256

10.  Lack of allelic loss at the multiple endocrine neoplasia type 1 (MEN-1) gene locus in a pancreatic ductal (non-endocrine) adenocarcinoma of a patient with the MEN-1 syndrome.

Authors:  C Bordi; A Falchetti; C Azzoni; T D'Adda; A Morelli; A Peracchia; M L Brandi
Journal:  Virchows Arch       Date:  1995       Impact factor: 4.064
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