Literature DB >> 7942863

Exclusion of linkage between autosomal dominant split hand/split foot and markers from chromosome 7q: further evidence for genetic heterogeneity.

F Gurrieri, M Genuardi, P Chiurazzi, G Gillessen-Kaesbach, G Neri.   

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Year:  1994        PMID: 7942863      PMCID: PMC1918293     

Source DB:  PubMed          Journal:  Am J Hum Genet        ISSN: 0002-9297            Impact factor:   11.025


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  12 in total

1.  Deletion of 7q22 and ectrodactyly.

Authors:  H Rivera; J Sanchez-Corona; V R Burgos-Fuentes; M J Melendez-Ruiz
Journal:  Genet Couns       Date:  1991

2.  Ectro-amelia syndrome associated with an interstitial deletion of 7q.

Authors:  M A Morey; R R Higgins
Journal:  Am J Med Genet       Date:  1990-01

3.  A computer program for linkage analysis of general human pedigrees.

Authors:  J Ott
Journal:  Am J Hum Genet       Date:  1976-09       Impact factor: 11.025

4.  Interstitial long-arm deletion of chromosome 7 and ectrodactyly.

Authors:  E H Tajara; M Varella-Garcia; A C Gusson
Journal:  Am J Med Genet       Date:  1989-02

5.  Split hand/split foot anomaly in a family segregating a balanced translocation with breakpoint on 7q22.1.

Authors:  M Genuardi; M G Pomponi; V Sammito; A Bellussi; M Zollino; G Neri
Journal:  Am J Med Genet       Date:  1993-11-01

6.  Evidence for locus heterogeneity in human autosomal dominant split hand/split foot malformation.

Authors:  S E Palmer; S W Scherer; M Kukolich; E M Wijsman; L C Tsui; K Stephens; J P Evans
Journal:  Am J Hum Genet       Date:  1994-07       Impact factor: 11.025

7.  Report and abstracts of the First International Workshop on Human Chromosome 7 Mapping 1993.

Authors:  K H Grzeschik; L C Tsui; E D Green
Journal:  Cytogenet Cell Genet       Date:  1994

8.  Easy calculations of lod scores and genetic risks on small computers.

Authors:  G M Lathrop; J M Lalouel
Journal:  Am J Hum Genet       Date:  1984-03       Impact factor: 11.025

9.  EC syndrome in a girl with paracentric inversion (7)(q22.1;q36.3).

Authors:  S Akita; H Kuratomi; K Abe; N Harada; N Mukae; N Niikawa
Journal:  Clin Dysmorphol       Date:  1993-01       Impact factor: 0.816

10.  Two chromosome 7 dinucleotide repeat polymorphisms at gene loci epidermal growth factor receptor (EGFR) and pro alpha 2 (I) collagen (COL1A2).

Authors:  D D Chi; A V Hing; C Helms; T Steinbrueck; S K Mishra; H Donis-Keller
Journal:  Hum Mol Genet       Date:  1992-05       Impact factor: 6.150

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  2 in total

1.  Bilateral split hand/foot malformation and inv(7)(p22q21.3).

Authors:  J M Cobben; J B Verheij; W H Eisma; P H Robinson; R P Zwierstra; B Leegte; S Castedo
Journal:  J Med Genet       Date:  1995-05       Impact factor: 6.318

2.  Split hand/split foot malformation, deafness, and mental retardation with a complex cytogenetic rearrangement involving 7q21.3.

Authors:  J Ignatius; S Knuutila; S W Scherer; B Trask; J Kere
Journal:  J Med Genet       Date:  1996-06       Impact factor: 6.318

  2 in total

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