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Literature DB >> 7951309

Phenotypic diversity, allelic series and modifier genes.

G Romeo, V A McKusick.

Abstract

Mesh：

Year: 1994 PMID： 7951309 DOI： 10.1038/ng0894-451

Source DB: PubMed Journal: Nat Genet ISSN： 1061-4036 Impact factor: 38.330

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17 in total

1. Discovery Genetics - The History and Future of Spontaneous Mutation Research.

Authors: Muriel T Davisson; David E Bergstrom; Laura G Reinholdt; Leah Rae Donahue
Journal: Curr Protoc Mouse Biol Date: 2012-06-01

2. Locating a modifier gene of Ovum mutant through crosses between DDK and C57BL/6J inbred strains in mice.

Authors: Jing Tan; Gen Di Song; Jia Sheng Song; Shi Hao Ren; Chun Li Li; Zhen Yu Zheng; Wei Dong Zhao
Journal: J Genet Date: 2016-06 Impact factor: 1.166

Review 3. Multiple endocrine neoplasia syndromes, children, Hirschsprung's disease and RET.

Authors: S W Moore; M G Zaahl
Journal: Pediatr Surg Int Date: 2008-03-26 Impact factor: 1.827

4. Discordant phenotype in siblings with X-linked agammaglobulinemia.

Authors: M J Bykowsky; R N Haire; Y Ohta; H Tang; S S Sung; E S Veksler; J M Greene; S M Fu; G W Litman; K E Sullivan
Journal: Am J Hum Genet Date: 1996-03 Impact factor: 11.025

5. Analysis of the RET, GDNF, EDN3, and EDNRB genes in patients with intestinal neuronal dysplasia and Hirschsprung disease.

Authors: R Gath; A Goessling; K M Keller; S Koletzko; W Coerdt; H Müntefering; S Wirth; R M Hofstra; L Mulligan; C Eng; A von Deimling
Journal: Gut Date: 2001-05 Impact factor: 23.059

6. Multiple endocrine neoplasia type 2A/localized cutaneous lichen amyloidosis associated with malignant pheochromocytoma and ganglioneuroma.

Authors: S Gullu; A Gursoy; M F Erdogan; S Dizbaysak; G Erdogan; N Kamel
Journal: J Endocrinol Invest Date: 2005-09 Impact factor: 4.256

Phenotypic diversity, allelic series and modifier genes.

1. Discovery Genetics - The History and Future of Spontaneous Mutation Research.

2. Locating a modifier gene of Ovum mutant through crosses between DDK and C57BL/6J inbred strains in mice.

Review 3. Multiple endocrine neoplasia syndromes, children, Hirschsprung's disease and RET.

4. Discordant phenotype in siblings with X-linked agammaglobulinemia.

5. Analysis of the RET, GDNF, EDN3, and EDNRB genes in patients with intestinal neuronal dysplasia and Hirschsprung disease.

6. Multiple endocrine neoplasia type 2A/localized cutaneous lichen amyloidosis associated with malignant pheochromocytoma and ganglioneuroma.

Review 7. Strain background effects and genetic modifiers of hearing in mice.

8. Mutations in the gene for X-linked adrenoleukodystrophy in patients with different clinical phenotypes.

9. A high-resolution linkage map of the lethal spotting locus: a mouse model for Hirschsprung disease.

10. A high-resolution genetic map of mouse chromosome 15 encompassing the Dominant megacolon (Dom) locus.