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1
Triploidy 69, XXX in a stillborn girl
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Article
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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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2
Quantification of all fetal nucleated cells in maternal blood in different cases of aneuploidies
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Article
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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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3
Original Article: Quantification of all fetal nucleated cells in maternal blood in different cases of aneuploidies
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Article
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Original Article: Quantification of all fetal nucleated cells in maternal blood in different cases of aneuploidies

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

Blackwell Munksgaard, 2005 ;ISSN: 0009-9163 ;EISSN: 1399-0004 ;DOI: 10.1111/j.1399-0004.2005.00564.x

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4
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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5
Cytogenetics of recurrent abortions
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Article
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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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6
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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7
Familial 5/14 translocation with triple X and 47,XY + 14q
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Article
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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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8
Parental and meiotic origin of triploidy in the embryonic and fetal periods
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Article
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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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9
Clinical implementation of NIPT - technical and biological challenges
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Clinical implementation of NIPT - technical and biological challenges

Clinical genetics, 2016-05, Vol.89 (5), p.523-530 [Peer Reviewed Journal]

2015 John Wiley & Sons A/S. Published by John Wiley & Sons Ltd ;2015 John Wiley & Sons A/S. Published by John Wiley & Sons Ltd. ;2016 John Wiley & Sons A/S. Published by John Wiley & Sons Ltd ;ISSN: 0009-9163 ;EISSN: 1399-0004 ;DOI: 10.1111/cge.12598 ;PMID: 25867715

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10
Autism spectrum disorders: a qualitative study of attitudes toward prenatal genetic testing and termination decisions of affected pregnancies
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Autism spectrum disorders: a qualitative study of attitudes toward prenatal genetic testing and termination decisions of affected pregnancies

Clinical genetics, 2015-08, Vol.88 (2), p.122-128 [Peer Reviewed Journal]

2014 John Wiley & Sons A/S. Published by John Wiley & Sons Ltd ;2014 John Wiley & Sons A/S. Published by John Wiley & Sons Ltd. ;2015 John Wiley & Sons A/S. Published by John Wiley & Sons Ltd ;ISSN: 0009-9163 ;EISSN: 1399-0004 ;DOI: 10.1111/cge.12504 ;PMID: 25251361

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11
First-trimester spontaneous pregnancy loss - molecular analysis using multiplex ligation-dependent probe amplification
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Article
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First-trimester spontaneous pregnancy loss - molecular analysis using multiplex ligation-dependent probe amplification

Clinical genetics, 2016-05, Vol.89 (5), p.620-624 [Peer Reviewed Journal]

2016 John Wiley & Sons A/S. Published by John Wiley & Sons Ltd ;2016 John Wiley & Sons A/S. Published by John Wiley & Sons Ltd. ;ISSN: 0009-9163 ;EISSN: 1399-0004 ;DOI: 10.1111/cge.12727 ;PMID: 26748861

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12
Genetic analysis of first-trimester miscarriages with a combination of cytogenetic karyotyping, microsatellite genotyping and arrayCGH
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Genetic analysis of first-trimester miscarriages with a combination of cytogenetic karyotyping, microsatellite genotyping and arrayCGH

Clinical genetics, 2009-02, Vol.75 (2), p.133-140 [Peer Reviewed Journal]

2009 The Authors Journal compilation © 2009 Blackwell Munksgaard ;2009 INIST-CNRS ;Journal compilation © 2009 Blackwell Munksgaard ;ISSN: 0009-9163 ;EISSN: 1399-0004 ;DOI: 10.1111/j.1399-0004.2008.01131.x ;PMID: 19215247 ;CODEN: CLGNAY

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13
Fertility and pregnancy outcome in Danish women with Turner syndrome
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Article
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Fertility and pregnancy outcome in Danish women with Turner syndrome

Clinical genetics, 2002-01, Vol.61 (1), p.35-39 [Peer Reviewed Journal]

2002 INIST-CNRS ;ISSN: 0009-9163 ;EISSN: 1399-0004 ;DOI: 10.1034/j.1399-0004.2002.610107.x ;PMID: 11903353 ;CODEN: CLGNAY

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14
Triple aneuploidy in spontaneous abortions
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Article
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Triple aneuploidy in spontaneous abortions

Clinical genetics, 1999-07, Vol.56 (1), p.103-104 [Peer Reviewed Journal]

ISSN: 0009-9163 ;EISSN: 1399-0004 ;DOI: 10.1034/j.1399-0004.1999.560118.x ;PMID: 10466428

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15
Chromosome studies and fertility treatment in women with ovarian failure
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Article
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Chromosome studies and fertility treatment in women with ovarian failure

Clinical genetics, 1989-08, Vol.36 (2), p.81-91 [Peer Reviewed Journal]

1990 INIST-CNRS ;ISSN: 0009-9163 ;EISSN: 1399-0004 ;DOI: 10.1111/j.1399-0004.1989.tb03169.x ;PMID: 2766572 ;CODEN: CLGNAY

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16
X-chromosome polysomy in the female: personal experience and review of the literature
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Article
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X-chromosome polysomy in the female: personal experience and review of the literature

Clinical genetics, 1983-05, Vol.23 (5), p.341-349 [Peer Reviewed Journal]

ISSN: 0009-9163 ;EISSN: 1399-0004 ;DOI: 10.1111/j.1399-0004.1983.tb00443.x ;PMID: 6342877

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17
Normal testicular histology in a mid-trimester 49,XXXXY fetus
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Article
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Normal testicular histology in a mid-trimester 49,XXXXY fetus

Clinical genetics, 1995-06, Vol.47 (6), p.331-331 [Peer Reviewed Journal]

ISSN: 0009-9163 ;EISSN: 1399-0004 ;DOI: 10.1111/j.1399-0004.1995.tb03977.x ;PMID: 7554371

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18
Identification of the parental origin of polysomy in two 49,XXXXY cases
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Article
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Identification of the parental origin of polysomy in two 49,XXXXY cases

Clinical genetics, 1997-06, Vol.51 (6), p.426-429 [Peer Reviewed Journal]

1997 INIST-CNRS ;ISSN: 0009-9163 ;EISSN: 1399-0004 ;DOI: 10.1111/j.1399-0004.1997.tb02504.x ;PMID: 9237509 ;CODEN: CLGNAY

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19
Recombination aneusomy of chromosome 5 associated with multiple severe congenital malformations
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Article
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Recombination aneusomy of chromosome 5 associated with multiple severe congenital malformations

Clinical genetics, 1986-10, Vol.30 (4), p.285-292 [Peer Reviewed Journal]

1987 INIST-CNRS ;ISSN: 0009-9163 ;EISSN: 1399-0004 ;DOI: 10.1111/j.1399-0004.1986.tb00608.x ;PMID: 3791677 ;CODEN: CLGNAY

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20
The fetal pathology of the XXXXY-syndrome
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Article
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The fetal pathology of the XXXXY-syndrome

Clinical genetics, 1986-09, Vol.30 (3), p.213-218 [Peer Reviewed Journal]

1987 INIST-CNRS ;ISSN: 0009-9163 ;EISSN: 1399-0004 ;DOI: 10.1111/j.1399-0004.1986.tb00597.x ;PMID: 3780037 ;CODEN: CLGNAY

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Results 1 - 20 of 24  for All Library Resources

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