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1
A case of full triploidy (69,XXX) of paternal origin with unusually long survival time
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A case of full triploidy (69,XXX) of paternal origin with unusually long survival time

Clinical genetics, 1993-02, Vol.43 (2), p.79-82 [Peer Reviewed Journal]

1993 Blackwell Munksgaard ;1993 INIST-CNRS ;ISSN: 0009-9163 ;EISSN: 1399-0004 ;DOI: 10.1111/j.1399-0004.1993.tb04432.x ;PMID: 8448906 ;CODEN: CLGNAY

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2
Earlier finishing of Xp21.2 subband replication of the inactive X chromosome in Rett syndrome girl but not in her 47,XXX mother
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Earlier finishing of Xp21.2 subband replication of the inactive X chromosome in Rett syndrome girl but not in her 47,XXX mother

Clinical genetics, 1997-08, Vol.52 (2), p.120-125 [Peer Reviewed Journal]

1997 INIST-CNRS ;ISSN: 0009-9163 ;EISSN: 1399-0004 ;DOI: 10.1111/j.1399-0004.1997.tb02529.x ;PMID: 9298748 ;CODEN: CLGNAY

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3
Lymphocyte proliferation in a 31-week premature neonate with 69, XXX chromosomal constitution
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Lymphocyte proliferation in a 31-week premature neonate with 69, XXX chromosomal constitution

Clinical genetics, 1983-07, Vol.24 (1), p.26-28 [Peer Reviewed Journal]

ISSN: 0009-9163 ;EISSN: 1399-0004 ;DOI: 10.1111/j.1399-0004.1983.tb00064.x ;PMID: 6616943

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4
Fetal gonadal histology in XXXXY, XYY and XXX syndromes
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Fetal gonadal histology in XXXXY, XYY and XXX syndromes

Clinical genetics, 1980-07, Vol.18 (1), p.1-5 [Peer Reviewed Journal]

ISSN: 0009-9163 ;EISSN: 1399-0004 ;DOI: 10.1111/j.1399-0004.1980.tb01356.x ;PMID: 7418248

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5
Triploidy syndrome: A report on two live-born (69, XXY) and one still-born (69, XXX) infants
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Triploidy syndrome: A report on two live-born (69, XXY) and one still-born (69, XXX) infants

Clinical genetics, 1976-01, Vol.9 (1), p.43-50 [Peer Reviewed Journal]

ISSN: 0009-9163 ;EISSN: 1399-0004 ;DOI: 10.1111/j.1399-0004.1976.tb01548.x ;PMID: 174849

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6
Triploidy 69, XXX in a stillborn girl
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Triploidy 69, XXX in a stillborn girl

Clinical genetics, 1973-01, Vol.4 (3), p.210-212 [Peer Reviewed Journal]

ISSN: 0009-9163 ;EISSN: 1399-0004 ;DOI: 10.1111/j.1399-0004.1973.tb01144.x ;PMID: 4765204

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7
Motor nerve conduction in 47, XXY and 48, XXYY males, and 47, XXX and 45, X females
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Motor nerve conduction in 47, XXY and 48, XXYY males, and 47, XXX and 45, X females

Clinical genetics, 1974-01, Vol.6 (3), p.205-215 [Peer Reviewed Journal]

ISSN: 0009-9163 ;EISSN: 1399-0004 ;DOI: 10.1111/j.1399-0004.1974.tb00653.x ;PMID: 4426136

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8
Quantification of all fetal nucleated cells in maternal blood in different cases of aneuploidies
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Quantification of all fetal nucleated cells in maternal blood in different cases of aneuploidies

Clinical genetics, 2006-02, Vol.69 (2), p.145-154 [Peer Reviewed Journal]

2006 INIST-CNRS ;ISSN: 0009-9163 ;EISSN: 1399-0004 ;DOI: 10.1111/j.1399-0004.2005.00564.x ;PMID: 16433695 ;CODEN: CLGNAY

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9
Karyotype/phenotype correlation in females with short stature
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Karyotype/phenotype correlation in females with short stature

Clinical genetics, 1992-03, Vol.41 (3), p.147-151 [Peer Reviewed Journal]

1992 INIST-CNRS ;ISSN: 0009-9163 ;EISSN: 1399-0004 ;DOI: 10.1111/j.1399-0004.1992.tb03652.x ;PMID: 1563089 ;CODEN: CLGNAY

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10
Fragile site Xq27.3 in a family without mental retardation
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Fragile site Xq27.3 in a family without mental retardation

Clinical genetics, 1992-01, Vol.41 (1), p.33-35 [Peer Reviewed Journal]

1992 INIST-CNRS ;ISSN: 0009-9163 ;EISSN: 1399-0004 ;DOI: 10.1111/j.1399-0004.1992.tb03625.x ;PMID: 1633644 ;CODEN: CLGNAY

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11
Two fertile Turner women in a family
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Two fertile Turner women in a family

Clinical genetics, 1984-12, Vol.26 (6), p.591-596 [Peer Reviewed Journal]

1985 INIST-CNRS ;ISSN: 0009-9163 ;EISSN: 1399-0004 ;DOI: 10.1111/j.1399-0004.1984.tb01109.x ;PMID: 6499271 ;CODEN: CLGNAY

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12
Cytogenetics of recurrent abortions
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Cytogenetics of recurrent abortions

Clinical genetics, 1983-04, Vol.23 (4), p.294-297 [Peer Reviewed Journal]

ISSN: 0009-9163 ;EISSN: 1399-0004 ;DOI: 10.1111/j.1399-0004.1983.tb01879.x ;PMID: 6851220

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13
A cytogenetic survey of 14,069 newborn infants. I. Incidence of chromosome abnormalities
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A cytogenetic survey of 14,069 newborn infants. I. Incidence of chromosome abnormalities

Clinical genetics, 1975-10, Vol.8 (4), p.223-243 [Peer Reviewed Journal]

ISSN: 0009-9163 ;EISSN: 1399-0004 ;DOI: 10.1111/j.1399-0004.1975.tb01498.x ;PMID: 1183067

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14
A cytogenetic survey of 449 patients in a Japanese institution for the mentally retarded
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A cytogenetic survey of 449 patients in a Japanese institution for the mentally retarded

Clinical genetics, 1980-01, Vol.17 (3), p.177-182 [Peer Reviewed Journal]

ISSN: 0009-9163 ;EISSN: 1399-0004 ;DOI: 10.1111/j.1399-0004.1980.tb00130.x ;PMID: 6444857

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15
Aneuploidy in recurrent spontaneous aborters: the tendency to parental nondisjunction
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Aneuploidy in recurrent spontaneous aborters: the tendency to parental nondisjunction

Clinical genetics, 1984-07, Vol.26 (1), p.43-45 [Peer Reviewed Journal]

1985 INIST-CNRS ;ISSN: 0009-9163 ;EISSN: 1399-0004 ;DOI: 10.1111/j.1399-0004.1984.tb00786.x ;PMID: 6467654 ;CODEN: CLGNAY

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16
Anthropometry in sex chromosome abnormality
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Anthropometry in sex chromosome abnormality

Clinical genetics, 1974-01, Vol.5 (2), p.96-106 [Peer Reviewed Journal]

ISSN: 0009-9163 ;EISSN: 1399-0004 ;DOI: 10.1111/j.1399-0004.1974.tb01668.x ;PMID: 4829429

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17
Familial 5/14 translocation with triple X and 47,XY + 14q
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Familial 5/14 translocation with triple X and 47,XY + 14q

Clinical genetics, 1981-07, Vol.20 (1), p.40-43 [Peer Reviewed Journal]

ISSN: 0009-9163 ;EISSN: 1399-0004 ;DOI: 10.1111/j.1399-0004.1981.tb01804.x ;PMID: 7296947

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18
Oral and dental development in X chromosome aneuploidy
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Oral and dental development in X chromosome aneuploidy

Clinical genetics, 1985-02, Vol.27 (2), p.122-126 [Peer Reviewed Journal]

1985 INIST-CNRS ;ISSN: 0009-9163 ;EISSN: 1399-0004 ;DOI: 10.1111/j.1399-0004.1985.tb00198.x ;PMID: 3978846 ;CODEN: CLGNAY

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19
The electrocardiogram and sex chromosome aneuploidy
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The electrocardiogram and sex chromosome aneuploidy

Clinical genetics, 1974-01, Vol.6 (1), p.1-14 [Peer Reviewed Journal]

ISSN: 0009-9163 ;EISSN: 1399-0004 ;DOI: 10.1111/j.1399-0004.1974.tb00623.x ;PMID: 4426125

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20
Parental and meiotic origin of triploidy in the embryonic and fetal periods
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Parental and meiotic origin of triploidy in the embryonic and fetal periods

Clinical genetics, 2000-09, Vol.58 (3), p.192-200 [Peer Reviewed Journal]

2000 INIST-CNRS ;ISSN: 0009-9163 ;EISSN: 1399-0004 ;DOI: 10.1034/j.1399-0004.2000.580306.x ;PMID: 11076041 ;CODEN: CLGNAY

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