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The G deletion syndromes.
J Pediatr. 1970 Oct;77(4):658-63
PMID: 5454712
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[Familial mosaicism with G ring].
Humangenetik. 1969;7(4):275-86
PMID: 5365569
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Pairing at the chromosomal level.
J Cell Physiol. 1967 Oct;70(2):Suppl:119-46
PMID: 5625725
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The Production of Homozygous Deficient Tissues with Mutant Characteristics by Means of the Aberrant Mitotic Behavior of Ring-Shaped Chromosomes.
Genetics. 1938 Jul;23(4):315-76
PMID: 17246891
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On the Stabilization of a Ring Chromosome in Maize.
Genetics. 1958 Jan;43(1):86-91
PMID: 17247744
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A Closed X Chromosome in Drosophila Melanogaster.
Genetics. 1933 May;18(3):250-83
PMID: 17246691
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Evidence for Sister-Strand Crossing over in Maize.
Genetics. 1953 May;38(3):251-60
PMID: 17247437
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FAMILIAL VARIANT AUTOSOMES: NEW HUMAN CYTOGENETIC MARKERS.
Bull Johns Hopkins Hosp. 1965 Jun;116:396-402
PMID: 14300779
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[Behavior of the ring chromosomes in mitosis and miosis in Antirrhinum majus L].
Chromosoma. 1959;10(2):144-62
PMID: 13652350
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A 45,XX,21--child: attempt at a cytological and clinical interpretation of the karyotype.
J Med Genet. 1972 Mar;9(1):110-5
PMID: 5025474
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Points of exchange in a human no. 5 ring chromosome.
Cytogenet Cell Genet. 1973;12(1):35-9
PMID: 4122450
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A child with a 21-ring chromosome, 45XX,21minus-46,XX,21r investigated with the banding technique.
Humangenetik. 1973;18(4):315-9
PMID: 4125992
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Karyotype 45,XX,-21/46,XX,21q-in an infant with symptoms of G-deletion syndrome I.
J Med Genet. 1974 Dec;11(4):389-93
PMID: 4140913
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A case of a girl with a 21 ring chromosome.
Hum Hered. 1974;24(1):100-4
PMID: 4136482
-
Studies on human meiotic chromosomes from testicular tissue.
Lancet. 1966 Mar 26;1(7439):679-82
PMID: 4159599
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Ring-G chromosome, a new G-deletion syndrome?
Am J Dis Child. 1968 Apr;115(4):489-93
PMID: 4296014
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Identification by fluorescent microscopy of the abnormal chromosomes associated with the G-deletion syndromes.
Am J Hum Genet. 1973 Jan;25(1):77-81
PMID: 4265215
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An information and discriminant analysis of fingerprint patterns pertaining to identification of mongolism and mental retardation.
Am J Hum Genet. 1968 Jan;20(1):24-43
PMID: 4230139
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[22-ring chromosome: identification by controlled heat denaturation].
Ann Genet. 1973 Sep;16(3):193-7
PMID: 4543208
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Identification by fluorescence of two G rings: (46,XY,21r) G deletion syndrome I and (46, XX, 22r) G deletion syndrome II.
Ann Genet. 1972 Dec;15(4):265
PMID: 4539485
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21 monosomy in a retarded female infant.
J Med Genet. 1974 Dec;11(4):386-9
PMID: 4443988
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Dermatoglyphics in the G deletion syndromes.
J Ment Defic Res. 1973 Jun;17(2):149-56
PMID: 4794903
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A "G" deletion syndrome anti-mongolism.
Acta Paediatr Scand. 1973 Mar;62(2):216-20
PMID: 4691464
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Monozygotic twins with ring chromosome 22.
J Med Genet. 1973 Mar;10(1):85-9
PMID: 4697858
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Identification of 21r and 22r chromosomes by quinacrine fluorescence.
Clin Genet. 1972;3(4):264-70
PMID: 5054320
-
G-deletion syndrome II.
Humangenetik. 1972;14(2):164-6
PMID: 5026850
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Partial monosomy of a G group chromosome (45,XY,G-46,XY,Gr): report of a new case.
Ann Genet. 1971 Mar;14(1):7-12
PMID: 5314299
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Double monosomy mosaicism (45,X-45, XX,21-) in a retarded child with multiple congenital malformations.
Cytogenetics. 1971;10(6):404-12
PMID: 5146417
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Comparative behavior of ring chromosomes.
Am J Hum Genet. 1970 May;22(3):304-18
PMID: 5445002