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نمایش تعداد 1-5 از 5

Statistical Evidence: A Likelihood Paradigm

نوع: Journal Paper

نویسنده : Veronica J. Vieland; Susan E. Hodge

ناشر: American Society of Human Genetics

سال: 1998

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Transaldolase Deficiency: Liver Cirrhosis Associated with a New Inborn Error in the Pentose Phosphate Pathway

نوع: Journal Paper

نویسنده : Nanda M. Verhoeven; Jojanneke H.J. Huck; Birthe Roos; Eduard A. Struys; Gajja S. Salomons; Adriaan C. Douwes; Marjo S. van der Knaap; Cornelis Jakobs

ناشر: American Society of Human Genetics

سال: 2001

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A Missense Single-Nucleotide Polymorphism in a Gene Encoding a Protein Tyrosine Phosphatase (PTPN22) Is Associated with Rheumatoid Arthritis

نوع: Journal Paper

نویسنده : Ann B. Begovich; Victoria E.H. Carlton; Lee A. Honigberg; Steven J. Schrodi; Anand P. Chokkalingam; Heather C. Alexander; Kristin G. Ardlie; Qiqing Huang; Ashley M. Smith; Jill M. Spoerke; Marion T. Conn; Monica Chang; Sheng-Yung P. Chang; Randall K. Saiki; Joseph J. Catanese; Diane U. Leong; Veronica E. Garcia; Linda B. McAllister; Douglas A. Jeffery; Annette T. Lee; Franak Batliwalla; Elaine Remmers; Lindsey A. Criswell; Michael F. Seldin; Daniel L. Kastner; Christopher I. Amos; John J. Sninsk

ناشر: American Society of Human Genetics

سال: 2004

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A Regulatory Path Associated with X-Linked Intellectual Disability and Epilepsy Links KDM5C to the Polyalanine Expansions in ARX

نوع: Journal Paper

نویسنده : Poeta, Loredana; Fusco, Francesca; Drongitis, Denise; Shoubridge, Cheryl; Manganelli, Genesia; Filosa, Stefania; Paciolla, Mariateresa; Courtney, Monica; Collombat, Patrick; Lioi, Maria Brigida; Gecz, Jozef; Ursini, Matilde Valeria; Miano, Maria Giuseppina

ناشر: American Society of Human Genetics

سال: 2013

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Quantitative Analysis of Fetal DNA in Maternal Plasma and Serum: Implications for Noninvasive Prenatal Diagnosis

نوع: Journal Paper

نویسنده : Y. M. Dennis Lo; Mark S.C. Tein; Tze K. Lau; Christopher J. Haines; Tse N. Leung; Priscilla M.K. Poon; James S. Wainscoat; Philip J. Johnson; Allan M.Z. Chang; N. Magnus Hjelm

ناشر: American Society of Human Genetics

سال: 1998

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Statistical Evidence: A Likelihood Paradigm

Transaldolase Deficiency: Liver Cirrhosis Associated with a New Inborn Error in the Pentose Phosphate Pathway

A Missense Single-Nucleotide Polymorphism in a Gene Encoding a Protein Tyrosine Phosphatase (PTPN22) Is Associated with Rheumatoid Arthritis

A Regulatory Path Associated with X-Linked Intellectual Disability and Epilepsy Links KDM5C to the Polyalanine Expansions in ARX

Quantitative Analysis of Fetal DNA in Maternal Plasma and Serum: Implications for Noninvasive Prenatal Diagnosis

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Statistical Evidence: A Likelihood Paradigm

Transaldolase Deficiency: Liver Cirrhosis Associated with a New Inborn Error in the Pentose Phosphate Pathway

A Missense Single-Nucleotide Polymorphism in a Gene Encoding a Protein Tyrosine Phosphatase (PTPN22) Is Associated with Rheumatoid Arthritis

A Regulatory Path Associated with X-Linked Intellectual Disability and Epilepsy Links KDM5C to the Polyalanine Expansions in ARX

Quantitative Analysis of Fetal DNA in Maternal Plasma and Serum: Implications for Noninvasive Prenatal Diagnosis