DEVELOPMENTAL HEMOGLOBIN ANOMALIES IN A CHROMOSOMAL TRIPLICATION: D1 TRISOMY SYNDROME.
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MicroRNA-15a and -16-1 act via MYB to elevate fetal hemoglobin expression in human trisomy 13Human embryonic, fetal, and adult hemoglobins have different subunit interface strengths. Correlation with lifespan in the red cell.A human embryonic hemoglobin inhibits Hb S polymerization in vitro and restores a normal phenotype to mouse models of sickle cell disease.Autosomal trisomy syndromes: a detailed study of 27 cases of Edwards' syndrome and 27 cases of Patau's syndrome.Chromosome 15 abnormality in a mentally retarded adult.Immunological profile in a chromosome 18 deletion syndrome with IgA deficiencyTrisomy 13 syndrome in Chinese infants. Clinical findings and incidenceDouble autosomal trisomy and mosaicism for three cell lines in man: coexisting trisomy 13-15, trisomy 17-18, and a minority cell line trisomic for a chromosome of both groupsA partial D-trisomy-normal mosaic femaleCongenital chromosomal syndromes. A model for pathogenesis.Localization of genes on chromosome 13: analysis of two kindreds.Trisomy 13 with a 13-X translocation.QUANTITATIVE STUDIES ON A2, SICKLE CELL, AND FETAL HEMOGLOBINS IN NEGROES WITH MONGOLISM, WITH OBSERVATIONS ON TRANSLOCATION MONGOLISM IN NEGROESThe switch from fetal to adult hemoglobinMolecular basis of β thalassemia and potential therapeutic targets.The North American Opossum (Didelphis marsupialis) is an excellent model for the study of hemoglobin ontogeny.Control mechanisms of the conversion from synthesis of embryonic to adult hemoglobin.Haemoglobin and red cell enzyme changes in juvenile myeloid leukaemia.Genetic Basis and Genetic Modifiers of β-Thalassemia and Sickle Cell Disease.A familial 3-18 reciprocal translocation resulting in chromosome duplication-deficiency (3?plus-18q minus).Changes in the Chromosome and Haemoglobin Patterns in a Patient with Erythro-leukaemia.
P2860
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P2860
DEVELOPMENTAL HEMOGLOBIN ANOMALIES IN A CHROMOSOMAL TRIPLICATION: D1 TRISOMY SYNDROME.
description
1964 nî lūn-bûn
@nan
1964 թուականի Յունուարին հրատարակուած գիտական յօդուած
@hyw
1964 թվականի հունվարին հրատարակված գիտական հոդված
@hy
1964年の論文
@ja
1964年論文
@yue
1964年論文
@zh-hant
1964年論文
@zh-hk
1964年論文
@zh-mo
1964年論文
@zh-tw
1964年论文
@wuu
name
DEVELOPMENTAL HEMOGLOBIN ANOMALIES IN A CHROMOSOMAL TRIPLICATION: D1 TRISOMY SYNDROME.
@ast
DEVELOPMENTAL HEMOGLOBIN ANOMALIES IN A CHROMOSOMAL TRIPLICATION: D1 TRISOMY SYNDROME.
@en
DEVELOPMENTAL HEMOGLOBIN ANOMALIES IN A CHROMOSOMAL TRIPLICATION: D1 TRISOMY SYNDROME.
@nl
type
label
DEVELOPMENTAL HEMOGLOBIN ANOMALIES IN A CHROMOSOMAL TRIPLICATION: D1 TRISOMY SYNDROME.
@ast
DEVELOPMENTAL HEMOGLOBIN ANOMALIES IN A CHROMOSOMAL TRIPLICATION: D1 TRISOMY SYNDROME.
@en
DEVELOPMENTAL HEMOGLOBIN ANOMALIES IN A CHROMOSOMAL TRIPLICATION: D1 TRISOMY SYNDROME.
@nl
prefLabel
DEVELOPMENTAL HEMOGLOBIN ANOMALIES IN A CHROMOSOMAL TRIPLICATION: D1 TRISOMY SYNDROME.
@ast
DEVELOPMENTAL HEMOGLOBIN ANOMALIES IN A CHROMOSOMAL TRIPLICATION: D1 TRISOMY SYNDROME.
@en
DEVELOPMENTAL HEMOGLOBIN ANOMALIES IN A CHROMOSOMAL TRIPLICATION: D1 TRISOMY SYNDROME.
@nl
P2093
P2860
P356
P1476
DEVELOPMENTAL HEMOGLOBIN ANOMALIES IN A CHROMOSOMAL TRIPLICATION: D1 TRISOMY SYNDROME.
@en
P2093
P2860
P356
10.1073/PNAS.51.1.89
P407
P577
1964-01-01T00:00:00Z