A PATIENT WITH 48 CHROMOSOMES (XYYY).
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Child↗
Biomedical subjects
P L TOWNES
Publications and source records attributed to P L TOWNES.
TRYPSINOGEN DEFICIENCY DISEASE.
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Amylases↗
AN XXYY VARIANT OF THE KLINEFELTER SYNDROME IN A PREPUBERTAL BODY.
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Child↗
A NEW CONGENITAL HEMOLYTIC ANEMIA WITH DEFORMED ERYTHROCYTES ("STOMATOCYTES") AND REMARKABLE SUSCEPTIBILITY OF ERYTHROCYTES TO COLD HEMOLYSIS IN VITRO. I. CLINICAL AND HEMATOLOGIC STUDIES.
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Adolescent↗
THE NONRANDOMNESS OF CHROMOSOMAL ABNORMALITIES. ASSOCIATION OF TRISOMY 18 AND DOWN'S SYNDROME.
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Adolescent↗
TRISOMY 17-18--AN EVALUATION OF PRECONCEPTIONAL PARENTAL IRRADIATION AS A POSSIBLE ETIOLOGIC FACTOR.
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Anal Canal↗
A PROBABLE G/G TRANSLOCATION TRISOMY.
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Growth↗
Observations on the pathology of the trisomy 17-18 syndrome.
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Chromosomes, Human, Pair 17↗
Trisomy 13-15 in a male infant.
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Chromosome Disorders↗
Familial occurrence of malrotation of the intestine.
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Humans↗
Trisomy 18 (16-18) associated with congenital glaucoma and optic atrophy.
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Chromosomes↗
Investigation of the defect in a variant of hereditary methemoglobinemia.
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Humans↗
Hereditary methemoglobinemia: a new variant exhibiting dominant inheritance of methemoglobin A.
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Hemoglobin A↗