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Pericentric inversion of chromosome 21. A possible further cytogenetic mechanism in mongolism.
Lancet. 1962 Jan 6;1(7219):21-3
PMID: 13901315
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CYTOGENETICS OF DOWN'S SYNDROME (MONGOLISM). I. DATA ON A CONSECUTIVE SERIES OF PATIENTS REFERRED FOR GENETIC COUNSELLING AND DIAGNOSIS.
Cytogenetics. 1965;4:171-85
PMID: 14332559
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The sites and relative frequencies of secondary constrictions in human somatic chromosomes.
Cytogenetics. 1962;1:325-43
PMID: 13944753
-
The satellited chromosomes of man with reference to the marfan syndrome.
Am J Hum Genet. 1963 Mar;15:11-8
PMID: 13952502
-
Chromosomal abnormalities and their relation to disease.
Can Med Assoc J. 1963 Mar 2;88:456-61
PMID: 14018845
-
A child with an extra small metacentric chromosome.
Ann Hum Genet. 1965 Nov;29(2):199-205
PMID: 5863841
-
Chromosome preparations of leukocytes cultured from human peripheral blood.
Exp Cell Res. 1960 Sep;20:613-6
PMID: 13772379
-
Enhancement of secondary constrictions and the heterochromatic X in human cells.
Cytogenetics. 1962;1:225-44
PMID: 13990973
-
ENLARGED CHROMOSOMAL SATELLITES ASSOCIATED WITH MENTAL RETARDATION AND DIGITAL ARCHES IN THREE GENERATIONS.
Ann Hum Genet. 1964 Sep;28:21-6
PMID: 14204849
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ENLARGED SHORT ARM OR SATELLITE REGION-A HERITABLE TRAIT PROBABLY UNASSOCIATED WITH DEVELOPMENTAL DISORDER.
Cytogenetics. 1963;2:129-39
PMID: 14099757
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THE ASSOCIATION OF SATELLITED CHROMOSOMES WITH SPECIFIC CHROMOSOMAL REGIONS IN CULTURED HUMAN SOMATIC CELLS.
Ann Hum Genet. 1963 Nov;27:143-56
PMID: 14081485
-
Enlarged satellites as a familial chromosome marker.
Am J Hum Genet. 1962 Jun;14:107-24
PMID: 13881132
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ENLARGED SHORT ARM OF A SMALL ACROCENTRIC CHROMOSOME IN GRANDFATHER, MOTHER AND CHILD, THE LATTER WITH DOWN'S SYNDROME.
Cytogenetics. 1964;3:441-51
PMID: 14267136
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THE HUMAN CHROMOSOMAL SATELLITES IN NORMAL PERSONS AND IN TWO PATIENTS WITH MARFAN'S SYNDROME.
Proc Natl Acad Sci U S A. 1960 Apr;46(4):532-9
PMID: 16590637
-
Normal variations in the human karyotype.
Trans N Y Acad Sci. 1962 Feb;24:372-82
PMID: 14474084
-
Abnormal length of chromosomes 21 and 22 in four patients with Marfan's syndrome.
Cytogenetics. 1962;1:5-19
PMID: 14453314
-
A familial chromosome abnormality associated with repeated abortions.
Cytogenetics. 1962;1:199-209
PMID: 13991943
-
A human skin culture technique used for cytological examinations.
Br J Exp Pathol. 1960 Feb;41:31-7
PMID: 14399879
-
Enlarged satellites and multiple malformations in the same pedigree.
Ann Hum Genet. 1961 Oct;25:159-62
PMID: 13889992
-
Familial occurrence of trisomy 22.
Am J Hum Genet. 1968 Mar;20(2):107-18
PMID: 5643178
-
Atypical acrocentric chromosomes in Negro and Caucasian Mongols.
Am J Hum Genet. 1967 Mar;19(2):162-73
PMID: 4225661
-
Chromosome studies on randomly chosen men and women.
Lancet. 1965 Sep 18;2(7412):561-2
PMID: 4158190
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[FAMILIAL OCCURRENCE OF AN ABNORMAL D-CHROMOSOME].
Cytogenetics. 1964;3:112-23
PMID: 14190610
-
The demonstration of secondary constrictions in human chromosomes by means of a new technique.
Am J Hum Genet. 1963 Mar;15:24-33
PMID: 13986623
-
CHROMOSOME STUDIES IN MONGOLOIDS AND THEIR FAMILIES.
Cytogenetics. 1963;2:61-75
PMID: 14099760
-
Partial-trisomy syndromes. I. Sturge-Weber's disease.
Am J Hum Genet. 1961 Sep;13:287-98
PMID: 13733242
-
A familial chromosome translocation associated with speech and mental retardation.
Am J Hum Genet. 1961 Mar;13:32-46
PMID: 13772378
-
Inheritance of marker chromosomes from a cytogenetic survey of congenital heart disease.
Ann Hum Genet. 1966 Jul;30(1):77-84
PMID: 4225589
-
Nucleolus-organisers in the causation of chromosomal anomalies in man.
Lancet. 1961 Jul 15;2(7194):123-6
PMID: 13730523
-
AN ABERRANT AUTOSOME (13-15) IN A HUMAN FEMALE AND HER FATHER, BOTH APPARENTLY NORMAL.
Cytogenetics. 1963;2:34-41
PMID: 14042837
-
CYTOGENETIC STUDIES IN LEUCOCYTES ON THE GENERAL POPULATION: SUBJECTS OF AGES 65 YEARS AND MORE.
Ann Hum Genet. 1964 Jun;27:353-65
PMID: 14175200