Results 1 - 20 of 102 for All Library Resources
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| 1 |
Material Type: Article
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Ullrich-turner syndrome in monozygotic twinsAmerican journal of medical genetics, 1983-08, Vol.15 (4), p.537-542 [Peer Reviewed Journal]Copyright © 1983 Wiley‐Liss, Inc., A Wiley Company ;ISSN: 0148-7299 ;EISSN: 1096-8628 ;DOI: 10.1002/ajmg.1320150403 ;PMID: 6684396Full text available |
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Sex chromosome mosaicism in gonads of a fetus with cystic hygroma and deletion of the short arm of Y chromosome including loss of SRYAmerican journal of medical genetics, 2001-08, Vol.102 (2), p.157-160 [Peer Reviewed Journal]Copyright © 2001 Wiley‐Liss, Inc. ;2002 INIST-CNRS ;Copyright 2001 Wiley-Liss, Inc. ;ISSN: 0148-7299 ;EISSN: 1096-8628 ;DOI: 10.1002/ajmg.1414 ;PMID: 11477609 ;CODEN: AJMGDAFull text available |
| 3 |
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Psychosocial competence of unselected young adults with sex chromosome abnormalitiesAmerican journal of medical genetics, 1999-04, Vol.88 (2), p.200-206 [Peer Reviewed Journal]Copyright © 1999 Wiley‐Liss, Inc. ;1999 INIST-CNRS ;ISSN: 0148-7299 ;EISSN: 1096-8628 ;DOI: 10.1002/(SICI)1096-8628(19990416)88:2<200::AID-AJMG18>3.0.CO;2-3 ;PMID: 10206242 ;CODEN: AJMGDAFull text available |
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Neuropsychological and functional cognitive skills of 35 unselected adults with sex chromosome abnormalitiesAmerican journal of medical genetics, 2001-09, Vol.102 (4), p.309-313 [Peer Reviewed Journal]Copyright © 2001 Wiley‐Liss, Inc. ;2002 INIST-CNRS ;Copyright 2001 Wiley-Liss, Inc. ;ISSN: 0148-7299 ;EISSN: 1096-8628 ;DOI: 10.1002/ajmg.1490 ;PMID: 11503155 ;CODEN: AJMGDAFull text available |
| 5 |
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Neuropsychological impairment in 42 adolescents with sex chromosome abnormalitiesAmerican journal of medical genetics, 1993-10, Vol.48 (3), p.169-173 [Peer Reviewed Journal]Copyright © 1993 Wiley‐Liss, Inc., A Wiley Company ;1994 INIST-CNRS ;ISSN: 0148-7299 ;EISSN: 1096-8628 ;DOI: 10.1002/ajmg.1320480312 ;PMID: 8291574 ;CODEN: AJMGDAFull text available |
| 6 |
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Dual-probe fluorescence in situ hybridization assay for detecting deletions associated with VCFS/DiGeorge syndrome I and DiGeorge syndrome II lociAmerican journal of medical genetics, 2000-04, Vol.91 (4), p.313-317 [Peer Reviewed Journal]Copyright © 2000 Wiley‐Liss, Inc. ;2000 INIST-CNRS ;Copyright 2000 Wiley-Liss, Inc. ;ISSN: 0148-7299 ;EISSN: 1096-8628 ;DOI: 10.1002/(SICI)1096-8628(20000410)91:4<313::AID-AJMG13>3.0.CO;2-U ;PMID: 10766989 ;CODEN: AJMGDAFull text available |
| 7 |
Material Type: Article
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47,XXX t(7;11)(p 11.2;q11.2) and 48,XXXX t(7;11)(p11.2;q11.2) in the same patientAmerican journal of medical genetics, 1992-02, Vol.42 (3), p.395-395 [Peer Reviewed Journal]Copyright © 1992 Wiley‐Liss, Inc., A Wiley Company ;ISSN: 0148-7299 ;EISSN: 1096-8628 ;DOI: 10.1002/ajmg.1320420332 ;PMID: 1536188Full text available |
| 8 |
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Segregation patterns and phenotypes of unbalanced offspring in a large family with (10;18) chromosome translocationAmerican journal of medical genetics, 1985-12, Vol.22 (4), p.727-742 [Peer Reviewed Journal]Copyright © 1985 Wiley‐Liss, Inc., A Wiley Company ;1986 INIST-CNRS ;ISSN: 0148-7299 ;EISSN: 1096-8628 ;DOI: 10.1002/ajmg.1320220409 ;PMID: 4073123 ;CODEN: AJMGDAFull text available |
| 9 |
Material Type: Article
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Hypoplastic left heart in a patient with 45,X/46,XX/47,XXX mosaicismAmerican journal of medical genetics, 1978, Vol.2 (4), p.341-343 [Peer Reviewed Journal]Copyright © 1978 Wiley‐Liss, Inc., A Wiley Company ;ISSN: 0148-7299 ;EISSN: 1096-8628 ;DOI: 10.1002/ajmg.1320020404 ;PMID: 263448Full text available |
| 10 |
Material Type: Article
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Duchenne muscular dystrophy in a girl with a 45, X/46, XX/47, XXX chromosome constitutionAmerican journal of medical genetics, 1986-10, Vol.25 (2), p.239-243 [Peer Reviewed Journal]Copyright © 1986 Wiley‐Liss, Inc., A Wiley Company ;1987 INIST-CNRS ;ISSN: 0148-7299 ;EISSN: 1096-8628 ;DOI: 10.1002/ajmg.1320250207 ;PMID: 3777022 ;CODEN: AJMGDAFull text available |
| 11 |
Material Type: Article
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Azoospermia and duplication 3qter as distinct consequences of a familial t(X;3) (q26;q13.2)American journal of medical genetics, 1985-04, Vol.20 (4), p.677-684 [Peer Reviewed Journal]Copyright © 1985 Wiley‐Liss, Inc., A Wiley Company ;1986 INIST-CNRS ;ISSN: 0148-7299 ;EISSN: 1096-8628 ;DOI: 10.1002/ajmg.1320200413 ;PMID: 3993688 ;CODEN: AJMGDAFull text available |
| 12 |
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A 48,XXXX female with absence of ovariesAmerican journal of medical genetics, 1980, Vol.6 (4), p.275-278 [Peer Reviewed Journal]Copyright © 1980 Wiley‐Liss, Inc., A Wiley Company ;ISSN: 0148-7299 ;EISSN: 1096-8628 ;DOI: 10.1002/ajmg.1320060404 ;PMID: 7211945Full text available |
| 13 |
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Holoprosencephaly: Examples of clinical variability and etiologic heterogeneityAmerican journal of medical genetics, 1990-10, Vol.37 (2), p.244-249 [Peer Reviewed Journal]Copyright © 1990 Wiley‐Liss, Inc., A Wiley Company ;1991 INIST-CNRS ;ISSN: 0148-7299 ;EISSN: 1096-8628 ;DOI: 10.1002/ajmg.1320370216 ;PMID: 2147361 ;CODEN: AJMGDAFull text available |
| 14 |
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Prevalence of the fragile X syndrome in African-AmericansAmerican journal of medical genetics, 2002-07, Vol.110 (3), p.226-233 [Peer Reviewed Journal]Copyright © 2002 Wiley‐Liss, Inc. ;2002 INIST-CNRS ;Copyright 2002 Wiley-Liss, Inc. ;ISSN: 0148-7299 ;EISSN: 1096-8628 ;DOI: 10.1002/ajmg.10427 ;PMID: 12116230 ;CODEN: AJMGDAFull text available |
| 15 |
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Prenatal diagnosis in 3,000 women for chromosome, X-linked, and metabolic disordersAmerican journal of medical genetics, 1982-01, Vol.11 (1), p.61-75 [Peer Reviewed Journal]Copyright © 1982 Wiley‐Liss, Inc., A Wiley Company ;ISSN: 0148-7299 ;EISSN: 1096-8628 ;DOI: 10.1002/ajmg.1320110109 ;PMID: 7065004Full text available |
| 16 |
Material Type: Article
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Failure to establish linkage on the X chromosome in 301 families with schizophrenia or schizoaffective disorderAmerican journal of medical genetics, 2000-06, Vol.96 (3), p.335-341 [Peer Reviewed Journal]Copyright © 2000 Wiley‐Liss, Inc. ;ISSN: 0148-7299 ;EISSN: 1096-8628 ;DOI: 10.1002/1096-8628(20000612)96:3<335::AID-AJMG20>3.0.CO;2-E ;PMID: 10898911Full text available |
| 17 |
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Investigation of a candidate gene for schizophrenia on Xq13 previously associated with mental retardation and hypothyroidismAmerican journal of medical genetics, 2000-06, Vol.96 (3), p.398-403 [Peer Reviewed Journal]Copyright © 2000 Wiley‐Liss, Inc. ;ISSN: 0148-7299 ;EISSN: 1096-8628 ;DOI: 10.1002/1096-8628(20000612)96:3<398::AID-AJMG30>3.0.CO;2-Z ;PMID: 10898921Full text available |
| 18 |
Material Type: Article
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Pregnancy outcome and prenatal diagnosis of sex chromosome abnormalities in Hawaii, 1986-1999American journal of medical genetics. Part A, 2003-06, Vol.119A (3), p.305-310 [Peer Reviewed Journal]Copyright © 2003 Wiley‐Liss, Inc. ;Copyright 2003 Wiley-Liss, Inc. ;ISSN: 1552-4825 ;EISSN: 1552-4833 ;DOI: 10.1002/ajmg.a.20150 ;PMID: 12784298Full text available |
| 19 |
Material Type: Article
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Epidemiology of triploidy in a population-based birth defects registry, Hawaii, 1986-1999American journal of medical genetics. Part A, 2003-06, Vol.119A (3), p.319-323 [Peer Reviewed Journal]Copyright © 2003 Wiley‐Liss, Inc. ;Copyright 2003 Wiley-Liss, Inc. ;ISSN: 1552-4825 ;EISSN: 1552-4833 ;DOI: 10.1002/ajmg.a.20152 ;PMID: 12784300Full text available |
| 20 |
Material Type: Article
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ProtocadherinX/Y, a candidate gene-pair for schizophrenia and schizoaffective disorder: A DHPLC investigation of genomic sequenceAmerican journal of medical genetics. Part B, Neuropsychiatric genetics, 2004-08, Vol.129B (1), p.1-9 [Peer Reviewed Journal]Copyright © 2004 Wiley‐Liss, Inc. ;Copyright 2004 Wiley-Liss, Inc. ;ISSN: 1552-4841 ;EISSN: 1552-485X ;DOI: 10.1002/ajmg.b.30036 ;PMID: 15274028Full text available |
Results 1 - 20 of 102 for All Library Resources
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Creation Date
- Before 1983 (10)
- 1983 To 1987 (15)
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- 1993 To 1998 (19)
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Subject
- Female (100)
- Biological And Medical Sciences (73)
- Medical Sciences (72)
- Male (48)
- Medical Genetics (47)
- Karyotyping (41)
- Chromosome Aberrations (33)
- Adult (32)
- Pregnancy (30)
- X Chromosome (29)
- Phenotype (26)
- Infant, Newborn (22)
- Mosaicism (20)
- Abnormalities, Multiple - Genetics (19)
- Trisomy (18)
- Genetics (18)
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Journal Title
- Am J Med Genet (2)
- Am. J. Med. Genet (1)
- American Journal Of Medical Genetics B (1)
- American Journal Of Medical Genetics Part A (4)
- American Journal Of Medical Genetics Part B: Neuropsychiatric Genetics (1)
- American Journal Of Medical Genetics. Part A (18)
- American Journal Of Medical Genetics. Part B, Neuropsychiatric Genetics (9)
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