(Q45265262)

11 December 2017

Anomaly in the gamma chain heterogeneity of the newborn (English)

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11 December 2017

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Huisman TH

1

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11 December 2017

Schroeder WA

2

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11 December 2017

Felice A

3

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11 December 2017

Powars D

4

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11 December 2017

Ringelhann B

5

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11 December 2017

language of work or name

English

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publication date

1 January 1977

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11 December 2017

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11 December 2017

265

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11 December 2017

63-65

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11 December 2017

5589

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https://scigraph.springernature.com/pub.10.1038/265063a0

11 December 2017

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cites work

Evidence for multiple structural genes for the gamma chain of human fetal hemoglobin

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7 January 2021

Evidence for four nonallelic structural genes for the γ chain of human fetal hemoglobin

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7 January 2021

Evidence for multiple structural genes for the gamma-chain of human fetal hemoglobin in hereditary persistence of fetal hemoglobin

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7 January 2021

Estimation of Small Percentages of Fœtal Hæmoglobin

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7 January 2021

A direct estimate of the number of human gamma-globin genes

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7 January 2021

The present status of the heterogeneity of fetal hemoglobin in beta-thalassemia: an attempt to unify some observations in thalassemia and related conditions

1 reference

7 January 2021

Chemical heterogeneity of fetal hemoglobin in subjects with sickle cell anemia, homozygous hb-c disease, sc-disease, and various combinations of hemoglobin variants

1 reference

7 January 2021

Significance of a new type of human fetal hemoglobin carrying a replacement isoleucine replaced by threonine at position 75 )E 19) of the gamma chain

1 reference

7 January 2021

Identifiers

DOI

10.1038/265063A0

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Dimensions Publication ID

11 December 2017

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