Medical Journals

Topic: Child

Journal: Clinical Genetics

Documents

A list of abstracts that contain a topic of "Child" and a journal name of "Clinical Genetics".

Osteogenesis Imperfecta: Clinical, Biochemical and Molecular Findings.

PMID: 16879195
Clinical Profiles of Four Patients with Rett Syndrome Carrying a Novel Exon 1 Mutation or Genomic Rearrangement in the Mecp2 Gene.

PMID: 16630165
Contribution of the Cftr Gene, the Pancreatic Secretory Trypsin Inhibitor Gene (Spink1) and the Cationic Trypsinogen Gene (Prss1) to the Etiology of Recurrent Pancreatitis.

PMID: 17489851
The Genotype-phenotype Correlation of Hereditary Multiple Exostoses.

PMID: 16879194
Identification of Novel Mutations in the Rsk2 Gene (Rps6ka3) in Patients with Coffin-lowry Syndrome.

PMID: 16879200
Young People's Experiences of Growing Up in a Family Affected by Huntington's Disease.

PMID: 17250660

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Medical Journals

Topic: Child

Journal: Clinical Genetics

Documents

Osteogenesis Imperfecta: Clinical, Biochemical and Molecular Findings.

Clinical Profiles of Four Patients with Rett Syndrome Carrying a Novel Exon 1 Mutation or Genomic Rearrangement in the Mecp2 Gene.

Contribution of the Cftr Gene, the Pancreatic Secretory Trypsin Inhibitor Gene (Spink1) and the Cationic Trypsinogen Gene (Prss1) to the Etiology of Recurrent Pancreatitis.

The Genotype-phenotype Correlation of Hereditary Multiple Exostoses.

Identification of Novel Mutations in the Rsk2 Gene (Rps6ka3) in Patients with Coffin-lowry Syndrome.

Young People's Experiences of Growing Up in a Family Affected by Huntington's Disease.

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