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[A new technic of analysis of the human karyotype].
C R Acad Sci Hebd Seances Acad Sci D. 1971 May 17;272(20):2638-40
PMID: 4104656
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The relationship between patterns of DNA replication and of quinacrine fluorescence in the human chromosome complement.
Chromosoma. 1971;35(3):326-41
PMID: 4109087
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Polymorphism of the human Y chromosomes: fluorescence microscopic studies on the sites of morphologic variation.
Clin Genet. 1972;3(2):116-22
PMID: 4115479
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Identification of partial 12 trisomy by quinacrine fluorescence.
J Pediatr. 1973 Feb;82(2):269-72
PMID: 4119313
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Polymorphism of human C-band heterochromatin. I. Frequency of variants.
Am J Hum Genet. 1973 Mar;25(2):181-92
PMID: 4120239
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DNA content and DNA-based centromeric index of the 24 human chromosomes.
Science. 1973 Mar 16;179(4078):1126-9
PMID: 4120257
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The mechanism of C- and G-banding of chromosomes.
Exp Cell Res. 1973 Mar 15;77(1):469-83
PMID: 4120442
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Chromosome structure as revealed by a combined chemical and immunochemical procedure.
Proc Natl Acad Sci U S A. 1973 Mar;70(3):804-7
PMID: 4123691
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[Polymorphism of human constitutive heterochromatin in metaphase chromosome A1].
Humangenetik. 1973 May 25;18(3):213-7
PMID: 4124200
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[Giemsa-R-banding analysis of the trisomy 9p and report of a new case].
Humangenetik. 1973 Apr 16;18(2):129-38
PMID: 4124236
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An unbalanced 4q-21q translocation identified by the R but not by the G and Q chromosome banding techniques.
Ann Genet. 1973 Mar;16(1):11-6
PMID: 4124663
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Letter: A new consistent chromosomal abnormality in chronic myelogenous leukaemia identified by quinacrine fluorescence and Giemsa staining.
Nature. 1973 Jun 1;243(5405):290-3
PMID: 4126434
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[New system of chromosome banding: the T bands (author's transl)].
Chromosoma. 1973 Apr 27;41(4):395-402
PMID: 4127019
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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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[Partial trisomy 11q identified by study, with heat controlled denaturation, of the paternal balanced translocation].
Ann Genet. 1972 Sep;15(3):167-72
PMID: 4539764
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Ring chromosome D (13) associated with multiple congenital malformations.
Ann Genet. 1973 Sep;16(3):157-66
PMID: 4543204
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Abnormalities of human sex chromosomes. I. A ring Y without mosaiciam.
Ann Genet. 1973 Dec;16(4):225-31
PMID: 4544085
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[Familial balanced translocation t(2; 13) (q32; q33) and partial trisomy 2q].
Ann Genet. 1973 Dec;16(4):255-8
PMID: 4544088
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[Ring chromosome 8 (46,XY, 8 r) in a boy with debility (author's transl)].
Klin Padiatr. 1973 May;185(3):187-91
PMID: 4795572
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[Evaluation of chromosome errors at the moment of conception].
Biomedicine. 1973 Sep;18(5):372-4
PMID: 4796238
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A new syndrome resulting from partial trisomy for the distal third of the long arm of chromosome 10.
J Pediatr. 1974 Apr;84(4):567-70
PMID: 4834252
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Identification and characterization of heterochromatic regions in the human metaphase and interphase nucleus.
Humangenetik. 1974 Mar 28;21(4):331-40
PMID: 4837300
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Brother and sister with trisomy 10p: a new syndrome.
Humangenetik. 1974;23(3):163-72
PMID: 4844639
-
Para-nucleolar position of the human Y chromosome in interphase nuclei.
Nature. 1971 Aug 20;232(5312):556-7
PMID: 4937496
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Quinacrine mustard fluorescence of human chromosomes: characterization of unusual translocations.
Am J Hum Genet. 1972 Mar;24(2):189-213
PMID: 5016511
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C 11-D 13-translocation in four generations.
Humangenetik. 1972;14(4):300-5
PMID: 5051753
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A case of partial 14 trisomy 47,XY,(14q-)+ and translocation t(9p+;14q-) in mother and brother.
J Med Genet. 1972 Sep;9(3):367-73
PMID: 5079109
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[4 cases of trisomy for the short arm of chromosome 9. Individualization of a new morbid entity].
Ann Genet. 1970 Dec;13(4):217-32
PMID: 5313386
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Possible role of heterochromatin in human aneuploidy. A hypothesis.
Humangenetik. 1965;1(3):307-10
PMID: 5330883
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[Observation of the 13-15 chromosome group in a ring (46,XY,15r)].
Humangenetik. 1971;11(4):295-9
PMID: 5550594
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Structural polymorphism in chromosome 17.
Nature. 1969 Jan 25;221(5178):387-8
PMID: 5764448
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[Deficiency on the short arms of a chromosome No. 4].
Humangenetik. 1965;1(5):397-413
PMID: 5868696
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Multiple congenital anomalies associated with a ring 3 chromosome and translocated 3/X chromosome.
Nature. 1966 Oct 8;212(5058):153-5
PMID: 5972207
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Ring 1 chromosome and dwarfism--a possible syndrome.
J Pediatr. 1967 Nov;71(5):719-22
PMID: 6054759
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A ring chromosome, diagnosed by quinacrine fluorescence as No. 9, in a mentally retarded girl.
Clin Genet. 1973;4(5):434-41
PMID: 4127395
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Partial trisomy of chromosome number 15 identified by trypsin-Giemsa banding.
Am J Ment Defic. 1973 Mar;77(5):571-8
PMID: 4703990
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Partial trisomy of chromosome 11: a case report.
Am J Ment Defic. 1973 Jan;77(4):383-8
PMID: 4706396
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A case of trisomy 9.
J Med Genet. 1973 Jun;10(2):184-7
PMID: 4714588
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A comparison between quinacrine fluorescence banding and 3H-thymidine incorporation patterns in human chromosomes.
Humangenetik. 1973 Mar 23;18(1):63-70
PMID: 4721340
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Variation in the nonfluorescent segment of long Y chromosome.
Humangenetik. 1973;18(4):285-90
PMID: 4732020
-
Banding analysis of abnormal karyotypes in spontaneous abortion.
Am J Hum Genet. 1973 Sep;25(5):539-47
PMID: 4741848
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Chromosome studies in 5,049 consecutive newborn children.
Clin Genet. 1973;4(4):333-43
PMID: 4747810
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Presumptive direct insertion within chromosome 2 in man.
Ann Hum Genet. 1973 Apr;36(4):367-73
PMID: 4748757
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Mapping human autosomes: assignment of the MN locus to a specific segment in the long arm of chromosome no. 2.
Science. 1973 Dec 21;182(4118):1261-2
PMID: 4752219
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[Pericentric inversion, inv(10), in a mother and aneusomy by recombination, inv(10), rec(10), in her son (author's transl)].
Cytogenet Cell Genet. 1973;12(4):245-53
PMID: 4752866
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Human Y-chromatin. 3. The nucleolus.
Exp Cell Res. 1973 Oct;81(2):468-73
PMID: 4758910
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Preferential location of x-ray induced chromosome breakage in the R-bands of human chromosomes.
Hereditas. 1973;74(1):57-67
PMID: 4758985
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Cytogenetics of malignant lymphomas. Studies utilising a Giemsa-banding technique.
Humangenetik. 1973 Dec 10;20(3):231-50
PMID: 4772077
-
New observations on the human and chimpanzee karyotypes. Identification of breakage points of pericentric inversions.
Humangenetik. 1973;20(2):151-7
PMID: 4785161
-
A partial trisomy of chromosome 1 in a family with a t(1q-;4q+) translocation.
Clin Genet. 1973 Jun;4(6):474-9
PMID: 4787838
-
Nonrandom arrangement of human chromatin: topography of disomic markers X, Y, and 1h plus 1.
Cytogenet Cell Genet. 1973;12(6):443-52
PMID: 4791997
-
Nonrandom chromosomal abnormalities in hematologic disorders of man.
Proc Natl Acad Sci U S A. 1975 Jan;72(1):152-6
PMID: 1054491
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The use of distribution functions to describe integrated density profiles of human chromosomes.
J Theor Biol. 1973 Aug 22;40(3):573-89
PMID: 4127830
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Satellite DNA.
J Med Genet. 1973 Sep;10(3):273-81
PMID: 4129952
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[Comparison of the structure of chromatids of Homo sapiens and Pan troglodytes (author's transl)].
Chromosoma. 1973;43(4):423-44
PMID: 4130182
-
Correlation of the fluorescent banding pattern and ultrastructure of a human chromosome.
Exp Cell Res. 1974 Mar 15;84(1):121-6
PMID: 4131762
-
Nonrandom distribution of chromosome breaks in Fanconi's anemia.
Cytogenet Cell Genet. 1973;12(6):423-34
PMID: 4134387
-
Karyotype of the chimpanzee, Pan troglodytes, based on measurements and banding pattern: comparison to the human karyotype.
Cytogenet Cell Genet. 1973;12(6):453-61
PMID: 4134388
-
Chromosome banding patterns in an infant with 13q minus syndrome.
Humangenetik. 1974 Mar 28;21(4):309-14
PMID: 4134627
-
An analysis of the break points of structural rearrangements in man.
J Med Genet. 1974 Mar;11(1):50-64
PMID: 4134839
-
Loss of DNA following C-banding procedures.
Cytogenet Cell Genet. 1973;12(6):414-22
PMID: 4134969
-
Translocation, t(4qminus;13qplus), in three generations resulting in partial trisomy of the long arm of chromosome 4 in the fourth generation.
J Med Genet. 1974 Jun;11(2):201-5
PMID: 4135220
-
Trisomy of the short arm of chromosome 17.
Humangenetik. 1974;23(3):213-7
PMID: 4135958
-
Frequency of 9qh+ and risk of chromosome aberrations in the progeny of individuals with 9qh+.
Humangenetik. 1974;21(3):211-6
PMID: 4136265
-
Colored reverse-banding of human chromosomes with acridine orange following alkaline-formalin treatment: densitometric validation and applications.
Humangenetik. 1974 Jul 15;23(2):119-30
PMID: 4136600
-
Sister chromatid exchanges, indices of human chromosome damage and repair: detection by fluorescence and induction by mitomycin C.
Proc Natl Acad Sci U S A. 1974 Aug;71(8):3162-6
PMID: 4137928
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[Effects of pH on the staining of human chromosomes with acridine orange].
Exp Cell Res. 1974 Oct;88(2):418-21
PMID: 4139029
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Different forms of incomplete trisomy 13. Mosaicism and partial trisomy for the proxim.
Humangenetik. 1974;22(4):287-98
PMID: 4139096
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A manyfold increase in sister chromatid exchanges in Bloom's syndrome lymphocytes.
Proc Natl Acad Sci U S A. 1974 Nov;71(11):4508-12
PMID: 4140506
-
Tentative localization of a Hageman (Factor XII) locus on 7q, probably the 7q35 band.
Humangenetik. 1974;24(3):197-200
PMID: 4140832
-
Partial trisomy 8: trisomy of the distal part of the long arm of chromosome number 8 plus (8q2) in a severely retarded and malformed girl.
Humangenetik. 1974;24(3):241-6
PMID: 4140835
-
Trisomy 12p due to familial t(12p-,6q plus) translocation.
Humangenetik. 1974;24(3):247-52
PMID: 4140836
-
A presumptive tetrasomy for the short arm of chromosome 9.
Humangenetik. 1974;25(3):163-70
PMID: 4141333
-
Mosaic-trisomy and pericentric inversion of chromosome 9 in a malformed boy.
Humangenetik. 1974;25(3):171-7
PMID: 4141334
-
Computerized chromosome identification by aid of the quinacrine mustard fluorescence technique.
Hereditas. 1972;67(1):103-10
PMID: 4142003
-
Autosomal polymorphisms.
Birth Defects Orig Artic Ser. 1974;10(10):19-29
PMID: 4142589
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"Cri du Chat" due to a ring-B chromosome.
Lancet. 1965 Nov 20;2(7421):1075-6
PMID: 4159145
-
[Partial trisomy 10 due to hereditary translocation t(1;10)(q44;q22)].
Humangenetik. 1973;18(4):321-7
PMID: 4200006
-
Position of the Duffy locus on chromosome 1 in relation to breakpoints for structural rearrangements.
Am J Hum Genet. 1974 Jan;26(1):93-102
PMID: 4204536
-
Trisomy for short arm of chromosome 20.
Humangenetik. 1974;23(3):219-22
PMID: 4210799
-
Precise identification of various chromosomal abnormalities.
Ann Hum Genet. 1973 Apr;36(4):375-9
PMID: 4270654
-
Probable trisomy 22 identified by fluorescent and trypsin-giemsa banding.
Ann Genet. 1973 Sep;16(3):189-92
PMID: 4271166
-
Down's syndrome. The possibility of a pathogenetic segment on chromosome no. 21.
Humangenetik. 1974 Jan 22;21(1):99-101
PMID: 4276065
-
Partial trisomy 8 (8q24) and the trisomy-8 syndrome.
Humangenetik. 1974;23(4):297-303
PMID: 4420964
-
21 monosomy in a retarded female infant.
J Med Genet. 1974 Dec;11(4):386-9
PMID: 4443988
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Compositional heterogeneity of human heterochromatin.
Proc Natl Acad Sci U S A. 1972 Jun;69(6):1464-6
PMID: 4504360
-
Assignment by deletion of human red cell acid phosphatase gene locus to the short arm of chromosome 2.
Nat New Biol. 1973 Jun 27;243(130):271-4
PMID: 4515493
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Deletion of the long arm of chromosome no. 7: tentative assignment of the Kidd (Jk) locus.
Clin Genet. 1973;4(4):360-8
PMID: 4518278
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[Ring chromosome 18. 18p-/18q- -deletion-syndrome].
Humangenetik. 1972;15(4):289-318
PMID: 4565746
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The structure and function of chromatin.
Adv Hum Genet. 1972;3:237-431
PMID: 4578264
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Genetics and human disease.
Hum Pathol. 1974 Jul;5(4):387-405
PMID: 4600308
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Radiation-induced non-random chromosome breakage.
Exp Cell Res. 1972 Dec;75(2):541-3
PMID: 4644257
-
Individualized human karyotyping through quantitative analysis.
Comput Biol Med. 1972 Oct;2(2):181-93
PMID: 4668647
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High resolution studies on the pattern of induced exchanges in the human karyotype.
Chromosoma. 1973;40(4):333-46
PMID: 4693087
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Non-random occurrence of 7-14 translocations in human lymphocyte cultures.
Nature. 1975 May 15;255(5505):241-5
PMID: 1143322
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[Study of somatic chromosomes from 9 mongoloid children].
C R Hebd Seances Acad Sci. 1959 Mar 16;248(11):1721-2
PMID: 13639368
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TRISOMY OF AUTOSOME 16.
Nature. 1963 Jul 27;199:404
PMID: 14058595
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[3 CASES OF PARTIAL DELETION OF THE SHORT ARM OF A 5 CHROMOSOME].
C R Hebd Seances Acad Sci. 1963 Nov 18;257:3098-102
PMID: 14095841
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INTERPHASE DEOXYRIBONUCLEIC ACID CONDENSATION, LATE DEOXYRIBONUCLEIC ACID REPLICATION, AND GENE INACTIVATION.
Nature. 1965 Jan 16;205:311-2
PMID: 14270734