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Genetic and epigenetic mechanisms of the Beckwith -Wiedemann syndrome

Niemitz, Emily L

2005

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ProQuest

Posterior fossa malformations and other CNS abnormalities observed in patients diagnosed with Beckwith-Wiedemann Syndrome

Gardiner, Kate

2011

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ProQuest

Genetic Syndromes with Pancreatic Manifestations

Surgical pathology clinics, 2016-12, Vol.9 (4), p.705

2016

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Molecular analysis of Simpson-Golabi-Behmel syndrome: An overgrowth condition associated with an increased risk of embryonal tumour

Xuan, Jian Ying

1995

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ProQuest

Atlas of Genetic Diagnosis and Counseling

Chen, Harold

1. Aufl., 2006

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Novel Insights into the Clinical and Genomic Characteristics of Congenital Hyperinsulinism

Hewat, Ti

2022

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ProQuest

Molecular study of mutations leading to Angelman syndrome

Beuten, Joke

1996

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ProQuest

Method Development and Implementation of Low-Pass Genome Sequencing to Identify Structural Variants in Undiagnosed Diseases

Zhang, Yanyan

2022

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Understanding Lineage Dependencies in Rhabdomyosarcoma

Cleary, Cristian

2023

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ProQuest

Characterization of the Wilms' tumor suppressor genewt1 and its role in disease

Bruening, Wendy

1997

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ProQuest

Copy-Number Variation and the Etiology of Chronic Diseases: Computational Detections, Laboratory Validations, and Public Health Relevance

Walsh, Kyle M

2011

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ProQuest

Molecular and genetic analysis of chromosome 15q11 -q13 and autism susceptibility

Nurmi, Erika Lynn

2003

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ProQuest

Genomic imprinting in human placental development

Zaragoza, Michael Vincent

1998

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ProQuest

Analysis of variable expressivity in neurofibromatosis 1

Szudek, Jacek

2001

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Gnas: A gene with a complex pattern of genomic imprinting

Kwan, Helen Choi Kam

1999

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ProQuest

The genetic and epigenetic regulation of insulin-like growth factor II gene expression in humans

Giannoukakis, Nick

1997

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ProQuest

Clear cell sarcoma of the kidney and congenital mesoblastic nephroma: Cellular and molecular characterization of primary tumors, tumor cell lines, and nude mouse xenografts delineate Wilms' tumor-distinct histopathogenetic properties

Brownlee, Noel Anderson

1998

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ProQuest

Pathobiology of germ cell tumors of the adult testis: Views and news

Looijenga, Leendert Hendrik-Jan

1994

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ProQuest

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Genetic and epigenetic mechanisms of the Beckwith -Wiedemann syndrome

Posterior fossa malformations and other CNS abnormalities observed in patients diagnosed with Beckwith-Wiedemann Syndrome

Genetic Syndromes with Pancreatic Manifestations

Molecular analysis of Simpson-Golabi-Behmel syndrome: An overgrowth condition associated with an increased risk of embryonal tumour

Atlas of Genetic Diagnosis and Counseling

Novel Insights into the Clinical and Genomic Characteristics of Congenital Hyperinsulinism

Molecular study of mutations leading to Angelman syndrome

Method Development and Implementation of Low-Pass Genome Sequencing to Identify Structural Variants in Undiagnosed Diseases

Understanding Lineage Dependencies in Rhabdomyosarcoma

Characterization of the Wilms' tumor suppressor genewt1 and its role in disease

Copy-Number Variation and the Etiology of Chronic Diseases: Computational Detections, Laboratory Validations, and Public Health Relevance

Molecular and genetic analysis of chromosome 15q11 -q13 and autism susceptibility

Genomic imprinting in human placental development

Analysis of variable expressivity in neurofibromatosis 1

Gnas: A gene with a complex pattern of genomic imprinting

The genetic and epigenetic regulation of insulin-like growth factor II gene expression in humans

Clear cell sarcoma of the kidney and congenital mesoblastic nephroma: Cellular and molecular characterization of primary tumors, tumor cell lines, and nude mouse xenografts delineate Wilms' tumor-distinct histopathogenetic properties

Pathobiology of germ cell tumors of the adult testis: Views and news

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