Am J Med Genet A[TA]http://www.unboundmedicine.com/medline/ebm/journal/Am_J_Med_Genet_AUnbound MEDLINE is a service provided by Unbound Medicine, Inc. that includes data and services from the U.S. National Library of Medicine's MEDLINE® and PubMed® databases.en-usUnbound Medicine, Inc.Crisponi syndrome in an Indian patient: A rare differential diagnosis for neonatal tetanus.http://www.unboundmedicine.com/medline/ebm/record/18837055/full_citation/Crisponi_syndrome_in_an_Indian_patient:_A_rare_differential_diagnosis_for_neonatal_tetanus_Thomas N, Danda S, Kumar M, et al. 
Crisponi syndrome in an Indian patient: A rare differential diagnosis for neonatal tetanus. [JOURNAL ARTICLE]
Am J Med Genet A 2008 Oct 3.
Full Citation | Find Related Articles Molecular characterization of a patient with 3p deletion syndrome and a review of the literature.http://www.unboundmedicine.com/medline/ebm/record/18837054/full_citation/Molecular_characterization_of_a_patient_with_3p_deletion_syndrome_and_a_review_of_the_literature_Fernandez TV, García-González IJ, Mason CE, et al. 
Molecular characterization of a patient with 3p deletion syndrome and a review of the literature. [JOURNAL ARTICLE]
Am J Med Genet A 2008 Oct 3.
Abstract | Full Citation | Find Related Articles Studies of gamma-aminobutyric acid type A receptor beta3 (GABRB3) and glutamic acid decarboxylase 67 (GAD67) with oral clefts.http://www.unboundmedicine.com/medline/ebm/record/18837046/full_citation/Studies_of_gamma_aminobutyric_acid_type_A_receptor_beta3__GABRB3__and_glutamic_acid_decarboxylase_67__GAD67__with_oral_clefts_Vieira AR, Howe A, Murray JC 
Studies of gamma-aminobutyric acid type A receptor beta3 (GABRB3) and glutamic acid decarboxylase 67 (GAD67) with oral clefts. [JOURNAL ARTICLE]
Am J Med Genet A 2008 Oct 3.
Full Citation | Find Related Articles Tetra-amelia and lung hypo/aplasia syndrome: New case report and review.http://www.unboundmedicine.com/medline/ebm/record/18837045/full_citation/Tetra_amelia_and_lung_hypo/aplasia_syndrome:_New_case_report_and_review_Sousa SB, Pina R, Ramos L, et al. 
Tetra-amelia and lung hypo/aplasia syndrome: New case report and review. [JOURNAL ARTICLE]
Am J Med Genet A 2008 Oct 3.
Abstract | Full CitationFamilial recurrence of SOX2 anophthalmia syndrome: Phenotypically normal mother with two affected daughters.http://www.unboundmedicine.com/medline/ebm/record/18831064/full_citation/Familial_recurrence_of_SOX2_anophthalmia_syndrome:_Phenotypically_normal_mother_with_two_affected_daughters_Schneider A, Bardakjian TM, Zhou J, et al. 
Familial recurrence of SOX2 anophthalmia syndrome: Phenotypically normal mother with two affected daughters. [JOURNAL ARTICLE]
Am J Med Genet A 2008 Oct 1.
Abstract | Full Citation | Find Related Articles All in the family: Disclosure of "unwanted" information to an adolescent to benefit a relative.http://www.unboundmedicine.com/medline/ebm/record/18831063/full_citation/All_in_the_family:_Disclosure_of_"unwanted"_information_to_an_adolescent_to_benefit_a_relative_Denny CC, Wilfond BS, Peters JA, et al. 
All in the family: Disclosure of "unwanted" information to an adolescent to benefit a relative. [JOURNAL ARTICLE]
Am J Med Genet A 2008 Oct 1.
Abstract | Full CitationGenotype-phenotype relationship for localization and age distribution of telangiectases in hereditary hemorrhagic telangiectasia.http://www.unboundmedicine.com/medline/ebm/record/18831062/full_citation/Genotype_phenotype_relationship_for_localization_and_age_distribution_of_telangiectases_in_hereditary_hemorrhagic_telangiectasia_Letteboer TG, Mager HJ, Snijder RJ, et al. 
Genotype-phenotype relationship for localization and age distribution of telangiectases in hereditary hemorrhagic telangiectasia. [JOURNAL ARTICLE]
Am J Med Genet A 2008 Oct 1.
Abstract | Full Citation | Find Related Articles Kapur-Toriello syndrome: Further delineation.http://www.unboundmedicine.com/medline/ebm/record/18831061/full_citation/Kapur_Toriello_syndrome:_Further_delineation_Yokoyama E, Martínez A, González-Del Angel A 
Kapur-Toriello syndrome: Further delineation. [JOURNAL ARTICLE]
Am J Med Genet A 2008 Oct 1.
Abstract | Full CitationRobinow syndrome: Phenotypic variability in a family with a novel intragenic ROR2 mutation.http://www.unboundmedicine.com/medline/ebm/record/18831060/full_citation/Robinow_syndrome:_Phenotypic_variability_in_a_family_with_a_novel_intragenic_ROR2_mutation_Brunetti-Pierri N, Del Gaudio D, Peters H, et al. 
Robinow syndrome: Phenotypic variability in a family with a novel intragenic ROR2 mutation. [JOURNAL ARTICLE]
Am J Med Genet A 2008 Oct 1.
Abstract | Full CitationType II autosomal recessive cutis laxa: Report of another patient and molecular studies concerning three candidate genes.http://www.unboundmedicine.com/medline/ebm/record/18819152/full_citation/Type_II_autosomal_recessive_cutis_laxa:_Report_of_another_patient_and_molecular_studies_concerning_three_candidate_genes_Scherrer DZ, Alexandrino F, Cintra ML, et al. 
Type II autosomal recessive cutis laxa: Report of another patient and molecular studies concerning three candidate genes. [JOURNAL ARTICLE]
Am J Med Genet A 2008 Sep 25.
Abstract | Full Citation