Literature DB >> 6026932

Haptoglobin: a locus on the D1 chromosome?

W B Bias, B R Migeon.   

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Year:  1967        PMID: 6026932      PMCID: PMC1706219     

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


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  8 in total

1.  DEOXYRIBONUCLEIC-ACID REPLICATION PATTERN OF TRISOMY D1.

Authors:  J J YUNIS; E B HOOK; M MAYER
Journal:  Lancet       Date:  1964-10-31       Impact factor: 79.321

2.  FAMILIAL VARIANT AUTOSOMES: NEW HUMAN CYTOGENETIC MARKERS.

Authors:  B R MIGEON
Journal:  Bull Johns Hopkins Hosp       Date:  1965-06

3.  Immune-electrophoretic demonstration of qualitative differences in human sera and their relation to the haptoglobins.

Authors:  J HIRSCHFELD
Journal:  Acta Pathol Microbiol Scand       Date:  1959

4.  Zone electrophoresis in starch gels: group variations in the serum proteins of normal human adults.

Authors:  O SMITHIES
Journal:  Biochem J       Date:  1955-12       Impact factor: 3.857

5.  Studies on Hereditary Gamma Globulin Factors: Evidence that Gm (b) in Whites and Negroes is not the Same and that Gm-like is Determined by an Allele at the Gm Locus.

Authors:  A G Steinberg; J A Wilson
Journal:  Am J Hum Genet       Date:  1963-03       Impact factor: 11.025

6.  Demonstration of the inherited serum group specific protein by acrylamide electrophoresis.

Authors:  F D Kitchin
Journal:  Proc Soc Exp Biol Med       Date:  1965 Aug-Sep

7.  Localization of haptoglobin and ABO.

Authors:  T W Hustinx; J B Bijlsma; L E Nijenhuis
Journal:  Nature       Date:  1965-07-17       Impact factor: 49.962

8.  SERUM PROTEIN ELECTROPHORESIS IN ACRYLAMIDE GEL: PATTERNS FROM NORMAL HUMAN SUBJECTS.

Authors:  A C PEACOCK; S L BUNTING; K G QUEEN
Journal:  Science       Date:  1965-03-19       Impact factor: 47.728

  8 in total
  13 in total

1.  Familial short arm deletion of chromosome no. 15.

Authors:  J J Hoo; U Hillig; H Cramer; S Hansen; F Hermann
Journal:  Humangenetik       Date:  1974

2.  Cytogenetic and linkage studies of a familial 15pplus variant.

Authors:  F E Yoder; W B Bias; D S Borgaonkar; G F Bahr; I I Yoder; O C Yoder; H M Golomb
Journal:  Am J Hum Genet       Date:  1974-09       Impact factor: 11.025

3.  Frequency of deletion of short arm satellites in acrocentric chromosomes.

Authors:  J Nielsen; U Friedrich; A B Hreidarsson
Journal:  J Med Genet       Date:  1974-06       Impact factor: 6.318

Review 4.  Population cytogenetics, assignment of gene loci in autosomes, karyotype-phenotype correlations. A progress report on human cytogenetics.

Authors:  E Passarge
Journal:  Humangenetik       Date:  1970

5.  Short arm deletion of chromosome 14.

Authors:  I Emerit; B Noel; M Thiriet; M Loubon; B Quack
Journal:  Humangenetik       Date:  1972

6.  Ring 13 chromosome with normal haptoglobin inheritance.

Authors:  J G Hollowell; L G Littlefield; A Dharmkrong-AT; G M Folger; C W Heath; G E Bloom
Journal:  J Med Genet       Date:  1971-06       Impact factor: 6.318

7.  Occurrence of a presumptive C-B translocation carrier [46,XY,t (? Cp-; Bp+)] in a family of D-G translocation carriers [45,D-,G-,t (DqGq)+].

Authors:  G H Thomas; W B Bias
Journal:  J Med Genet       Date:  1969-12       Impact factor: 6.318

8.  Retinoblastoma and deletion D (14) syndrome.

Authors:  M G Wilson; J Melnyk; J W Towner
Journal:  J Med Genet       Date:  1969-09       Impact factor: 6.318

9.  Localization of genes on chromosome 13: analysis of two kindreds.

Authors:  G E Bloom; P S Gerald
Journal:  Am J Hum Genet       Date:  1968-11       Impact factor: 11.025

10.  Two clonal cell populations (mosaicism) in a 46,XY male with mucolipidosis II (I-cell disease)--an autosomal recessive disorder.

Authors:  G H Thomas; C S Miller; K E Toomey; L W Reynolds; M L Reitman; A Varki; A Vannier; K N Rosebaum; W B Bias; B H Schofield
Journal:  Am J Hum Genet       Date:  1982-07       Impact factor: 11.025

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