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Literature DB >> 14476391

Genetics of spherocytosis.

N E MORTON, A A MACKINNEY, N KOSOWER, R F SCHILLING, M P GRAY.

Abstract

Keywords: ANEMIA, HEMOLYTIC/genetics; ERYTHROCYTES

Mesh：

Year: 1962 PMID： 14476391 PMCID： PMC1932277

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

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18 in total

1. Data on linkage of ovalocytosis and blood groups.

Authors: T FUJII; W C MOLONEY; N E MORTON
Journal: Am J Hum Genet Date: 1955-03 Impact factor: 11.025

2. Genetic tests under incomplete ascertainment.

Authors: N E MORTON
Journal: Am J Hum Genet Date: 1959-03 Impact factor: 11.025

3. Hereditary spherocytosis in the deer mouse. Its similarity to the human disease.

Authors: R ANDERSON; R R HUESTIS; A G MOTULSKY
Journal: Blood Date: 1960-04 Impact factor: 22.113

4. The mutational load due to detrimental genes in man.

Authors: N E MORTON
Journal: Am J Hum Genet Date: 1960-09 Impact factor: 11.025

5. A study of retinoblastoma in Ohio.

Authors: M T MACKLIN
Journal: Am J Hum Genet Date: 1960-03 Impact factor: 11.025

6. The detection and estimation of linkage between the genes for elliptocytosis and the Rh blood type.

Authors: N E MORTON
Journal: Am J Hum Genet Date: 1956-06 Impact factor: 11.025

7. Sequential tests for the detection of linkage.

Authors: N E MORTON
Journal: Am J Hum Genet Date: 1955-09 Impact factor: 11.025

8. Observations on inheritance and heterogeneity of chronic spherocytosis.

Authors: L E YOUNG
Journal: Trans Assoc Am Physicians Date: 1955

9. Atypical congenital haemolytic anaemia.

Authors: J V DACIE; P L MOLLISON; N RICHARDSON; J G SELWYN; L SHAPIRO
Journal: Q J Med Date: 1953-01

10. A genetic study in hereditary spherocytosis.

Authors: M ABRAMS; J D BATTLE
Journal: Am J Hum Genet Date: 1952-12 Impact factor: 11.025

11 in total

1. Localization of spherocytosis to chromosome 8 or 12 and report of a family with spherocytosis and a reciprocal translocation.

Authors: W J Kimberling; T Fulbeck; L Dixon; H A Lubs
Journal: Am J Hum Genet Date: 1975-09 Impact factor: 11.025

2. ESTIMATION OF PREVALENCE UNDER INCOMPLETE SELECTION.

Authors: I BARRAI; M P MI; N E MORTON; N YASUDA
Journal: Am J Hum Genet Date: 1965-05 Impact factor: 11.025

3. Spectrin/band 3 ratio as diagnostic tool in hereditary spherocytosis.

Authors: S Cutillo; L Pinto; B Nobili; E Miraglia del Giudice; A Iolascon
Journal: Eur J Pediatr Date: 1992-01 Impact factor: 3.183

Review 4. Human chromosome 8.

Authors: S Wood
Journal: J Med Genet Date: 1988-11 Impact factor: 6.318

5. Monogenic disorders.

Authors: C O Carter
Journal: J Med Genet Date: 1977-10 Impact factor: 6.318

6. Proteomic identification of erythrocyte membrane protein deficiency in hereditary spherocytosis.

Authors: Selen Peker; Nejat Akar; Duygu Ozel Demiralp
Journal: Mol Biol Rep Date: 2011-06-26 Impact factor: 2.316

7. A laparoscopic approach to partial splenectomy for children with hereditary spherocytosis.

Authors: S Dutta; V E Price; V Blanchette; J C Langer
Journal: Surg Endosc Date: 2006-10-05 Impact factor: 4.584

Review 8. Dogma disputed. Does reproductive compensation exist? An analysis of Rh data.

Authors: T E Reed
Journal: Am J Hum Genet Date: 1971-03 Impact factor: 11.025

9. Prevalence of increased osmotic fragility of erythrocytes in German blood donors: screening using a modified glycerol lysis test.

Authors: S W Eber; A Pekrun; A Neufeldt; W Schröter
Journal: Ann Hematol Date: 1992-02 Impact factor: 3.673

10. Hereditary spherocytosis in a malay patient with chronic haemolysis.

Authors: Muhammad Kamil Sheikh; Narazah Mohd Yusoff; Gurjeet Kaur; Farhat Aziz Khan
Journal: Malays J Med Sci Date: 2007-07