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1
THE PERSISTENCY IN EXPERIMENTAL POPULATIONS OF SECOND CHROMOSOME RECESSIVE LETHALS OBTAINED AFTER IRRADIATION OF SPERMATOGONIA AND SPERMATOZOA IN DROSOPHILA MELANOGASTER
THE PERSISTENCY IN EXPERIMENTAL POPULATIONS OF SECOND CHROMOSOME RECESSIVE LETHALS OBTAINED AFTER IRRADIATION OF SPERMATOGONIA AND SPERMATOZOA IN DROSOPHILA MELANOGASTER
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THE PERSISTENCY IN EXPERIMENTAL POPULATIONS OF SECOND CHROMOSOME RECESSIVE LETHALS OBTAINED AFTER IRRADIATION OF SPERMATOGONIA AND SPERMATOZOA IN DROSOPHILA MELANOGASTER

YTTERBORN, KARL H.

Hereditas, 1968-01, Vol.60 (1-2), p.33-71 [Periódico revisado por pares]

Oxford, UK: Blackwell Publishing Ltd

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2
Chromosomal Abnormalities in Patients With Autism Spectrum Disorders From Taiwan
Chromosomal Abnormalities in Patients With Autism Spectrum Disorders From Taiwan
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Chromosomal Abnormalities in Patients With Autism Spectrum Disorders From Taiwan

Liao, Hsiao-Mei ; Gau, Susan Shur-Fen ; Tsai, Wen-Che ; Fang, Jye-Siung ; Su, Ying-Cheng ; Chou, Miao-Chun ; Liu, Shih-Kai ; Chou, Wen-Jiun ; Wu, Yu-Yu ; Chen, Chia-Hsiang

American journal of medical genetics. Part B, Neuropsychiatric genetics, 2013-10, Vol.162B (7), p.734-741 [Periódico revisado por pares]

United States: Blackwell Publishing Ltd

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3
Prenatal Diagnosis of Sex Chromosome Abnormalities
Prenatal Diagnosis of Sex Chromosome Abnormalities
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Prenatal Diagnosis of Sex Chromosome Abnormalities

Milunsky, Jeff M ; Milunsky, Aubrey Milunsky, Aubrey ; Milunsky, Jeff M

Genetic Disorders and the Fetus, 2015, p.267-312

United States: John Wiley & Sons, Incorporated

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4
Neurodevelopmental variability in three young girls with a rare chromosomal disorder, 48, XXXX
Neurodevelopmental variability in three young girls with a rare chromosomal disorder, 48, XXXX
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Neurodevelopmental variability in three young girls with a rare chromosomal disorder, 48, XXXX

Samango-Sprouse, Carole ; Keen, Colleen ; Mitchell, Francie ; Sadeghin, Teresa ; Gropman, Andrea

American journal of medical genetics. Part A, 2015-10, Vol.167A (10), p.2251-2259 [Periódico revisado por pares]

United States: Blackwell Publishing Ltd

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5
Expanding the phenotype of Triple X syndrome: A comparison of prenatal versus postnatal diagnosis
Expanding the phenotype of Triple X syndrome: A comparison of prenatal versus postnatal diagnosis
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Expanding the phenotype of Triple X syndrome: A comparison of prenatal versus postnatal diagnosis

Wigby, Kristen ; D'Epagnier, Cheryl ; Howell, Susan ; Reicks, Amy ; Wilson, Rebecca ; Cordeiro, Lisa ; Tartaglia, Nicole

American journal of medical genetics. Part A, 2016-11, Vol.170A (11), p.2870-2881 [Periódico revisado por pares]

United States: Blackwell Publishing Ltd

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6
Mental health and behavioural problems in children with XXYY: a comparison with intellectual disabilities
Mental health and behavioural problems in children with XXYY: a comparison with intellectual disabilities
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Mental health and behavioural problems in children with XXYY: a comparison with intellectual disabilities

Srinivasan, R. ; Wolstencroft, J. ; Erwood, M. ; Raymond, F. L. ; Bree, M. ; Hall, J. ; Skuse, D.

Journal of intellectual disability research, 2019-05, Vol.63 (5), p.477-488 [Periódico revisado por pares]

England: Wiley Subscription Services, Inc

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7
Y chromosome gene copy number and lack of autism phenotype in a male with an isodicentric Y chromosome and absent NLGN4Y expression
Y chromosome gene copy number and lack of autism phenotype in a male with an isodicentric Y chromosome and absent NLGN4Y expression
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Y chromosome gene copy number and lack of autism phenotype in a male with an isodicentric Y chromosome and absent NLGN4Y expression

Ross, Judith L. ; Bloy, Luke ; Roberts, Timothy P. L. ; Miller, Judith ; Xing, Chao ; Silverman, Lawrence A. ; Zinn, Andrew R.

American journal of medical genetics. Part B, Neuropsychiatric genetics, 2019-10, Vol.180 (7), p.471-482 [Periódico revisado por pares]

Hoboken, USA: John Wiley & Sons, Inc

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8
Family experiences and attitudes about receiving the diagnosis of sex chromosome aneuploidy in a child
Family experiences and attitudes about receiving the diagnosis of sex chromosome aneuploidy in a child
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Family experiences and attitudes about receiving the diagnosis of sex chromosome aneuploidy in a child

Riggan, Kirsten A. ; Close, Sharron ; Allyse, Megan A.

American journal of medical genetics. Part C, Seminars in medical genetics, 2020-06, Vol.184 (2), p.404-413

Hoboken, USA: John Wiley & Sons, Inc

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9
Gene Copy Number Quantification of SHOX , VAMP7 , and SRY for the Detection of Sex Chromosome Aneuploidies in Neonates
Gene Copy Number Quantification of SHOX , VAMP7 , and SRY for the Detection of Sex Chromosome Aneuploidies in Neonates
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Gene Copy Number Quantification of SHOX , VAMP7 , and SRY for the Detection of Sex Chromosome Aneuploidies in Neonates

Ibarra-Ramírez, Marisol ; Lugo-Trampe, José de Jesús ; Campos-Acevedo, Luis Daniel ; Zamudio-Osuna, Michelle ; Torres-Muñoz, Iris ; Gómez-Puente, Viviana ; García-Castañeda, Gloria ; Arredondo-Vázquez, Patricia ; Rodríguez-Sánchez, Irám Pablo ; Schaeffer, S Elisa ; Velasco-Sepúlveda, Braulio Hernán ; Villarreal-Pérez, Jesús Zacarías ; Martínez-de-Villarreal, Laura Elia

Genetic testing and molecular biomarkers, 2020-06, Vol.24 (6), p.352-358 [Periódico revisado por pares]

United States: Mary Ann Liebert, Inc

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10
Early neurodevelopmental and medical profile in children with sex chromosome trisomies: Background for the prospective eXtraordinarY babies study to identify early risk factors and targets for intervention
Early neurodevelopmental and medical profile in children with sex chromosome trisomies: Background for the prospective eXtraordinarY babies study to identify early risk factors and targets for intervention
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Early neurodevelopmental and medical profile in children with sex chromosome trisomies: Background for the prospective eXtraordinarY babies study to identify early risk factors and targets for intervention

Tartaglia, Nicole ; Howell, Susan ; Davis, Shanlee ; Kowal, Karen ; Tanda, Tanea ; Brown, Mariah ; Boada, Cristina ; Alston, Amanda ; Crawford, Leah ; Thompson, Talia ; Rijn, Sophie ; Wilson, Rebecca ; Janusz, Jennifer ; Ross, Judith

American journal of medical genetics. Part C, Seminars in medical genetics, 2020-06, Vol.184 (2), p.428-443

Hoboken, USA: John Wiley & Sons, Inc

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