Warning: Undefined array key "mm" in /www/wwwroot/www.ai-bt.com/si.php on line 10 Deprecated: trim(): Passing null to parameter #1 ($string) of type string is deprecated in /www/wwwroot/www.ai-bt.com/si.php on line 10 Highly polymorphic locus D15S24 (CMW-1) maps to 15pter-q13. [HGM9 provisional no. D15S24].

× No keyword cloud information.

18 in total

1. Reciprocal translocation between the proximal regions of the long arms of chromosomes 13 and 15 resulting in unbalanced offspring: characterization by fluorescence in situ hybridization and DNA analysis.

Authors: K Mangelschots; B Van Roy; F Speleman; N Van Roy; J Gheuens; J Beuten; I Buntinx; M N Van Thienen; H Willekens; J Dumon
Journal: Hum Genet Date: 1992-06 Impact factor: 4.132

2. The anonymous probe pDX15 (D15S91) detects an RFLP with MspI.

Authors: X L Wen; K Carland-Saucier; M Hepburn; M Rabin
Journal: Nucleic Acids Res Date: 1990-12-11 Impact factor: 16.971

3. The frequency of uniparental disomy in Prader-Willi syndrome. Implications for molecular diagnosis.

Authors: M J Mascari; W Gottlieb; P K Rogan; M G Butler; D A Waller; J A Armour; A J Jeffreys; R L Ladda; R D Nicholls
Journal: N Engl J Med Date: 1992-06-11 Impact factor: 91.245

4. Molecular, cytogenetic, and clinical investigations of Prader-Willi syndrome patients.

Authors: W P Robinson; A Bottani; Y G Xie; J Balakrishman; F Binkert; M Mächler; A Prader; A Schinzel
Journal: Am J Hum Genet Date: 1991-12 Impact factor: 11.025

5. Somatic recombination rather than uniparental disomy suggested as another mechanism by which genetic imprinting may play a role in the etiology of Prader-Willi syndrome.

Authors: C A Gregory; J Schwartz; A J Kirkilionis; N Rudd; J L Hamerton
Journal: Hum Genet Date: 1991-11 Impact factor: 4.132

6. Molecular and cytogenetic studies of the Prader-Willi syndrome.

Authors: R J Trent; F Volpato; A Smith; R Lindeman; M K Wong; G Warne; E Haan
Journal: J Med Genet Date: 1991-10 Impact factor: 6.318

7. The tyrosinase-positive oculocutaneous albinism gene shows locus homogeneity on chromosome 15q11-q13 and evidence of multiple mutations in southern African negroids.

Authors: M A Kedda; G Stevens; P Manga; C Viljoen; T Jenkins; M Ramsay
Journal: Am J Hum Genet Date: 1994-06 Impact factor: 11.025

8. A molecular and cytogenetic study in Finnish Prader-Willi patients.

Authors: H Kokkonen; M Kähkönen; J Leisti
Journal: Hum Genet Date: 1995-05 Impact factor: 4.132

9. Trisomy 15 with loss of the paternal 15 as a cause of Prader-Willi syndrome due to maternal disomy.

Authors: S B Cassidy; L W Lai; R P Erickson; L Magnuson; E Thomas; R Gendron; J Herrmann
Journal: Am J Hum Genet Date: 1992-10 Impact factor: 11.025

10. Deletion breakpoints associated with the Prader-Willi and Angelman syndromes (15q11-q13) are not sites of high homologous recombination.

Authors: W P Robinson; R Spiegel; A A Schinzel
Journal: Hum Genet Date: 1993-03 Impact factor: 4.132