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Literature DB >> 14278486

GENETIC TESTS WITH A SEX-LINKED MARKER: GLUCOSE-6-PHOSPHATE DEHYDROGENASE.

Abstract

Entities: Gene

Keywords: BRAZIL; GENETICS, HUMAN; GENETICS, POPULATION; GLUCOSEPHOSPHATE DEHY- DROGENASE DEFICIENCY; GLUCOSEPHOSPHATE DEHYDROGENASE; SEX; STATISTICS

Mesh：

Substances：

Year: 1964 PMID： 14278486 DOI： 10.1101/sqb.1964.029.01.043

Source DB: PubMed Journal: Cold Spring Harb Symp Quant Biol ISSN： 0091-7451

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35 in total

Review 1. Alport syndrome, basement membranes and collagen.

Authors: C E Kashtan; M M Kleppel; R J Butkowski; A F Michael; A J Fish
Journal: Pediatr Nephrol Date: 1990-09 Impact factor: 3.714

2. Evidence that mutations in the X-linked DDP gene cause incompletely penetrant and variable skewed X inactivation.

Authors: R M Plenge; L Tranebjaerg; P K Jensen; C Schwartz; H F Willard
Journal: Am J Hum Genet Date: 1999-03 Impact factor: 11.025

3. X chromosome-inactivation patterns of 1,005 phenotypically unaffected females.

Authors: James M Amos-Landgraf; Amy Cottle; Robert M Plenge; Mike Friez; Charles E Schwartz; John Longshore; Huntington F Willard
Journal: Am J Hum Genet Date: 2006-07-27 Impact factor: 11.025

4. Variability of red cell phenotypes between and within individuals in an unbiased sample of 77 heterozygotes for G6PD deficiency in Sardinia.

Authors: A Rinaldi; G Filippi; M Siniscalco
Journal: Am J Hum Genet Date: 1976-09 Impact factor: 11.025

10. Studies on hemophilia A in Sardinia bearing on the problems of multiple allelism, carrier detection, and differential mutation rate in the two sexes.

Authors: G Filippi; P M Mannucci; R Coppola; A Farris; A Rinaldi; M Siniscalco
Journal: Am J Hum Genet Date: 1984-01 Impact factor: 11.025

GENETIC TESTS WITH A SEX-LINKED MARKER: GLUCOSE-6-PHOSPHATE DEHYDROGENASE.

Review 1. Alport syndrome, basement membranes and collagen.

2. Evidence that mutations in the X-linked DDP gene cause incompletely penetrant and variable skewed X inactivation.

3. X chromosome-inactivation patterns of 1,005 phenotypically unaffected females.

4. Variability of red cell phenotypes between and within individuals in an unbiased sample of 77 heterozygotes for G6PD deficiency in Sardinia.

5. Heritability of X chromosome--inactivation phenotype in a large family.

6. Quantitative studies of glucose-6-phosphate dehydrogenase.

7. On the incidence of unilateral and bilateral colour blindness in heterozygous females.

8. Do twin Lyons have larger spots?

9. A method for estimating the number of blastoderm cells which give rise to Drosophila imaginal discs.

10. Studies on hemophilia A in Sardinia bearing on the problems of multiple allelism, carrier detection, and differential mutation rate in the two sexes.