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1
Mutations Causing Familial Biparental Hydatidiform Mole Implicate C6orf221 as a Possible Regulator of Genomic Imprinting in the Human Oocyte
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Mutations Causing Familial Biparental Hydatidiform Mole Implicate C6orf221 as a Possible Regulator of Genomic Imprinting in the Human Oocyte

American journal of human genetics, 2011-09, Vol.89 (3), p.451-458 [Peer Reviewed Journal]

2011 The American Society of Human Genetics ;2015 INIST-CNRS ;Copyright © 2011 The American Society of Human Genetics. Published by Elsevier Inc. All rights reserved. ;Copyright Cell Press Sep 9, 2011 ;2011 The American Society of Human Genetics. Published by Elsevier Ltd. All right reserved. 2011 The American Society of Human Genetics ;ISSN: 0002-9297 ;EISSN: 1537-6605 ;DOI: 10.1016/j.ajhg.2011.08.002 ;PMID: 21885028 ;CODEN: AJHGAG

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2
Variation in the HLA-G Promoter Region Influences Miscarriage Rates
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Variation in the HLA-G Promoter Region Influences Miscarriage Rates

American journal of human genetics, 2003-06, Vol.72 (6), p.1425-1435 [Peer Reviewed Journal]

2003 The American Society of Human Genetics ;2003 INIST-CNRS ;2003 by The American Society of Human Genetics. All rights reserved. 2003 ;ISSN: 0002-9297 ;EISSN: 1537-6605 ;DOI: 10.1086/375501 ;PMID: 12721954 ;CODEN: AJHGAG

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3
Neonatal and Fetal Methylenetetrahydrofolate Reductase Genetic Polymorphisms: An Examination of C677T and A1298C Mutations
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Neonatal and Fetal Methylenetetrahydrofolate Reductase Genetic Polymorphisms: An Examination of C677T and A1298C Mutations

American journal of human genetics, 2000-10, Vol.67 (4), p.986-990 [Peer Reviewed Journal]

2000 The American Society of Human Genetics ;2000 INIST-CNRS ;2000 by The American Society of Human Genetics. All rights reserved. 2000 ;ISSN: 0002-9297 ;EISSN: 1537-6605 ;DOI: 10.1086/303082 ;PMID: 10958762 ;CODEN: AJHGAG

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4
Susceptibility Loci for Preeclampsia on Chromosomes 2p25 and 9p13 in Finnish Families
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Susceptibility Loci for Preeclampsia on Chromosomes 2p25 and 9p13 in Finnish Families

American journal of human genetics, 2003-01, Vol.72 (1), p.168-177 [Peer Reviewed Journal]

2003 The American Society of Human Genetics ;2003 INIST-CNRS ;2003 by The American Society of Human Genetics. All rights reserved. 2003 ;ISSN: 0002-9297 ;EISSN: 1537-6605 ;DOI: 10.1086/345311 ;PMID: 12474145 ;CODEN: AJHGAG

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5
Evidence for a Familial Pregnancy-Induced Hypertension Locus in the eNOS-Gene Region
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Evidence for a Familial Pregnancy-Induced Hypertension Locus in the eNOS-Gene Region

American journal of human genetics, 1997-08, Vol.61 (2), p.354-362 [Peer Reviewed Journal]

1997 The American Society of Human Genetics ;1997 INIST-CNRS ;Distributed under a Creative Commons Attribution 4.0 International License ;ISSN: 0002-9297 ;EISSN: 1537-6605 ;DOI: 10.1086/514843 ;PMID: 9311740 ;CODEN: AJHGAG

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6
Rapid Clearance of Fetal DNA from Maternal Plasma
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Rapid Clearance of Fetal DNA from Maternal Plasma

American journal of human genetics, 1999, Vol.64 (1), p.218-224 [Peer Reviewed Journal]

1999 The American Society of Human Genetics ;1999 INIST-CNRS ;ISSN: 0002-9297 ;EISSN: 1537-6605 ;DOI: 10.1086/302205 ;PMID: 9915961 ;CODEN: AJHGAG

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7
A Genome Scan in Families from Australia and New Zealand Confirms the Presence of a Maternal Susceptibility Locus for Pre-Eclampsia, on Chromosome 2
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A Genome Scan in Families from Australia and New Zealand Confirms the Presence of a Maternal Susceptibility Locus for Pre-Eclampsia, on Chromosome 2

American journal of human genetics, 2000-12, Vol.67 (6), p.1581-1585 [Peer Reviewed Journal]

2000 The American Society of Human Genetics ;2001 INIST-CNRS ;2000 by The American Society of Human Genetics. All rights reserved. 2000 ;ISSN: 0002-9297 ;EISSN: 1537-6605 ;DOI: 10.1086/316888 ;PMID: 11035632 ;CODEN: AJHGAG

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8
A Recurrent Deletion of DPY19L2 Causes Infertility in Man by Blocking Sperm Head Elongation and Acrosome Formation
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A Recurrent Deletion of DPY19L2 Causes Infertility in Man by Blocking Sperm Head Elongation and Acrosome Formation

American journal of human genetics, 2011-03, Vol.88 (3), p.351-361 [Peer Reviewed Journal]

2011 The American Society of Human Genetics ;2015 INIST-CNRS ;Copyright © 2011 The American Society of Human Genetics. Published by Elsevier Inc. All rights reserved. ;Copyright Cell Press Mar 11, 2011 ;Distributed under a Creative Commons Attribution 4.0 International License ;2011 The American Society of Human Genetics. Published by Elsevier Ltd. All right reserved. 2011 The American Society of Human Genetics ;ISSN: 0002-9297 ;EISSN: 1537-6605 ;DOI: 10.1016/j.ajhg.2011.02.007 ;PMID: 21397064 ;CODEN: AJHGAG

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9
Skewed X Chromosome Inactivation and Trisomic Spontaneous Abortion: No Association
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Skewed X Chromosome Inactivation and Trisomic Spontaneous Abortion: No Association

American journal of human genetics, 2009-08, Vol.85 (2), p.179-193 [Peer Reviewed Journal]

2009 The American Society of Human Genetics ;2009 INIST-CNRS ;Copyright University of Chicago, acting through its Press Aug 14, 2009 ;2009 The American Society of Human Genetics. Published by Elsevier Ltd. All right reserved.. 2009 The American Society of Human Genetics ;ISSN: 0002-9297 ;EISSN: 1537-6605 ;DOI: 10.1016/j.ajhg.2009.07.002 ;PMID: 19646676 ;CODEN: AJHGAG

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10
Intracytoplasmic Sperm Injection May Increase the Risk of Imprinting Defects
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Intracytoplasmic Sperm Injection May Increase the Risk of Imprinting Defects

American journal of human genetics, 2002-07, Vol.71 (1), p.162-164 [Peer Reviewed Journal]

2002 The American Society of Human Genetics ;2002 INIST-CNRS ;2002 by The American Society of Human Genetics. All rights reserved. 2002 ;ISSN: 0002-9297 ;EISSN: 1537-6605 ;DOI: 10.1086/341096 ;PMID: 12016591 ;CODEN: AJHGAG

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11
Comparative Genomic Hybridization in Combination with Flow Cytometry Improves Results of Cytogenetic Analysis of Spontaneous Abortions
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Comparative Genomic Hybridization in Combination with Flow Cytometry Improves Results of Cytogenetic Analysis of Spontaneous Abortions

American journal of human genetics, 2000-05, Vol.66 (5), p.1516-1521 [Peer Reviewed Journal]

2000 The American Society of Human Genetics ;2000 INIST-CNRS ;ISSN: 0002-9297 ;EISSN: 1537-6605 ;DOI: 10.1086/302878 ;PMID: 10741955 ;CODEN: AJHGAG

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12
Disentangling Fetal and Maternal Susceptibility for Pre-Eclampsia: A British Multicenter Candidate-Gene Study
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Disentangling Fetal and Maternal Susceptibility for Pre-Eclampsia: A British Multicenter Candidate-Gene Study

American journal of human genetics, 2005-07, Vol.77 (1), p.127-131 [Peer Reviewed Journal]

2005 The American Society of Human Genetics ;2005 INIST-CNRS ;Copyright University of Chicago, acting through its Press Jul 2005 ;2005 by The American Society of Human Genetics. All rights reserved. 2005 ;ISSN: 0002-9297 ;EISSN: 1537-6605 ;DOI: 10.1086/431245 ;PMID: 15889386 ;CODEN: AJHGAG

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13
Skewed X-Chromosome Inactivation Is Common in Fetuses or Newborns Associated with Confined Placental Mosaicism
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Skewed X-Chromosome Inactivation Is Common in Fetuses or Newborns Associated with Confined Placental Mosaicism

American journal of human genetics, 1997-12, Vol.61 (6), p.1353-1361 [Peer Reviewed Journal]

1997 The American Society of Human Genetics ;1998 INIST-CNRS ;ISSN: 0002-9297 ;EISSN: 1537-6605 ;DOI: 10.1086/301651 ;PMID: 9399909 ;CODEN: AJHGAG

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14
A genomewide linkage study of preeclampsia/eclampsia reveals evidence for a candidate region on 4q
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A genomewide linkage study of preeclampsia/eclampsia reveals evidence for a candidate region on 4q

American journal of human genetics, 1997-05, Vol.60 (5), p.1158-1167 [Peer Reviewed Journal]

1997 INIST-CNRS ;ISSN: 0002-9297 ;EISSN: 1537-6605 ;PMID: 9150163 ;CODEN: AJHGAG

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15
Rapid prenatal diagnosis of chromosomal aneuploidies by fluorescence in situ hybridization : clinical experience with 4,500 specimens
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Rapid prenatal diagnosis of chromosomal aneuploidies by fluorescence in situ hybridization : clinical experience with 4,500 specimens

American journal of human genetics, 1993-05, Vol.52 (5), p.854-865 [Peer Reviewed Journal]

1993 INIST-CNRS ;ISSN: 0002-9297 ;EISSN: 1537-6605 ;PMID: 8488836 ;CODEN: AJHGAG

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16
The natural history of cytogenetically abnormal fetuses detected at midtrimester amniocentesis which are not terminated electively: new data and estimates of the excess and relative risk of late fetal death associated with 47,+21 and some other abnormal karyotypes
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The natural history of cytogenetically abnormal fetuses detected at midtrimester amniocentesis which are not terminated electively: new data and estimates of the excess and relative risk of late fetal death associated with 47,+21 and some other abnormal karyotypes

American journal of human genetics, 1989-12, Vol.45 (6), p.855-861 [Peer Reviewed Journal]

1990 INIST-CNRS ;ISSN: 0002-9297 ;EISSN: 1537-6605 ;PMID: 2589318 ;CODEN: AJHGAG

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17
Cytogenetic analysis of 750 spontaneous abortions with the direct-preparation method of chorionic villi and its implications for studying genetic causes of pregnancy wastage
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Cytogenetic analysis of 750 spontaneous abortions with the direct-preparation method of chorionic villi and its implications for studying genetic causes of pregnancy wastage

American journal of human genetics, 1990-10, Vol.47 (4), p.656-663 [Peer Reviewed Journal]

1991 INIST-CNRS ;ISSN: 0002-9297 ;EISSN: 1537-6605 ;PMID: 2220806 ;CODEN: AJHGAG

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18
Cystic fibrosis heterozygote screening in 5,161 pregnant women
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Cystic fibrosis heterozygote screening in 5,161 pregnant women

American journal of human genetics, 1996-04, Vol.58 (4), p.823-835 [Peer Reviewed Journal]

1996 INIST-CNRS ;ISSN: 0002-9297 ;EISSN: 1537-6605 ;PMID: 8644747 ;CODEN: AJHGAG

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19
Rapid detection of chromosome aneuploidies in uncultured amniocytes by using fluorescence in situ hybridization (FISH)
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Rapid detection of chromosome aneuploidies in uncultured amniocytes by using fluorescence in situ hybridization (FISH)

American journal of human genetics, 1992-07, Vol.51 (1), p.55-65 [Peer Reviewed Journal]

1992 INIST-CNRS ;ISSN: 0002-9297 ;EISSN: 1537-6605 ;PMID: 1609805 ;CODEN: AJHGAG

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20
Decreased fecundability in hutterite couples sharing HLA-DR
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Decreased fecundability in hutterite couples sharing HLA-DR

American journal of human genetics, 1992, Vol.50 (1), p.6-14 [Peer Reviewed Journal]

1992 INIST-CNRS ;ISSN: 0002-9297 ;EISSN: 1537-6605 ;PMID: 1729895 ;CODEN: AJHGAG

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Results 1 - 20 of 60  for All Library Resources

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