Abnormalities of human sex chromosomes. II. Turner's syndrome associated with the mosaicism 45,X-46, XX-p.
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Adolescent↗
Biomedical subjects
F H Allen
Publications and source records attributed to F H Allen.
Abnormalities of human sex chromosomes. 3. Duplication in the long arm of the Y chromosome (45,X-46,XYg+) in Y-gonadal dysgenesis.
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17-Hydroxycorticosteroids↗
Partial deletion of the short arm of chromosome no. 4(4p-): clinical studies in five unrelated patients.
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Abnormalities, Multiple↗
Inhibition of anti-I sera by human milk.
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Anemia, Hemolytic↗
Direct evidence of mutation at the locus for galactose-1-phosphate uridyl transferase.
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Female↗
Absence of close linkage between the locus for Xg and the locus for anhidrotic ectodermal dysplasia.
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Blood Group Antigens↗
Further observations on the Matuhasi-Ogata phenomenon.
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Absorption↗
Autoradiographic studies of human chromosomes. II. Data concerning the position of the MN locus.
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Autoradiography↗
Presumptive C-15 translocation and familial large Y identified by autoradiography.
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Abnormalities, Multiple↗
Placental chorangiomata and mental deficiency in a child with 2/15 translocation: 46,XX,t(2q-;15q+).
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Adult↗
Some population and family data on the inheritance of red cell phosphoglucomutase.
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Erythrocytes↗
The 13q-deletion syndrome.
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Abnormalities, Multiple↗
MN blood-group locus: data concerning the possible chromosomal location.
Combined data derived from clinical, cytogenetic, and blood-grouping studies of one family suggest that the MN locus is on the long arm of either the No. 2 or the No. 4 chromosome.
Autoradiography↗
Clinical experience with three examples of anti-Yta1.
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Absorption↗
A second example of anti-Lan.
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Antibodies↗
Anti-Vel 2, a new antibody showing heterogeneity of Vel system antibodies.
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Alleles↗