American Journal of Medical Genetics: Vol 108, No 4

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Vascular birthmarks of infancy: Resolving nosologic confusion

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Vasculogenesis, angiogenesis, hemangiomas, and vascular malformations

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Van der Woude syndrome with sensorineural hearing loss, large craniofacial sinuses, dental pulp stones, and minor limb anomalies: Report of a four-generation Thai family

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Mixed clefting type in Rapp-Hodgkin syndrome

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Prediction by FISH analysis of the occurrence of Wilms tumor in aniridia patients

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Short bi-iliac distance in prenatal Ullrich-Turner syndrome

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Anticipation in a unique family with Charcot-Marie-Tooth syndrome and deafness: Delineation of the clinical features and review of the literature

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Further evidence for a third deafness gene within the DFNA2 locus

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Glypican 1 gene: Good candidate for brachydactyly type E

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Kallmann syndrome in a patient with congenital spherocytosis and an interstitial 8p11.2 deletion

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Molecular characterization of 22q11 deletion in a three-generation family with maternal transmission

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Girl with combined cellular immunodeficiency, pancytopenia, malformations, deletion 11q23.3 → qter, and trisomy 8q24.3 → qter

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Scalp defects, polythelia, microcephaly, and developmental delay: A New syndrome with apparent autosomal dominant inheritance

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Novel Igα (CD79a) gene mutation in a Turkish patient with B cell-deficient agammaglobulinemia

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Mosaic trisomy 8 as a cause of velopharyngeal insufficiency

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Two-loci ADA haplotypes in autistic disorder

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Genomic Regulatory Systems: Development and Evolution, by Eric H. Davidson

American Journal of Medical Genetics

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American Journal of Medical Genetics: Volume 108, Issue 4

Vascular birthmarks of infancy: Resolving nosologic confusion

Vasculogenesis, angiogenesis, hemangiomas, and vascular malformations

Van der Woude syndrome with sensorineural hearing loss, large craniofacial sinuses, dental pulp stones, and minor limb anomalies: Report of a four-generation Thai family

Mixed clefting type in Rapp-Hodgkin syndrome

Prediction by FISH analysis of the occurrence of Wilms tumor in aniridia patients

Short bi-iliac distance in prenatal Ullrich-Turner syndrome

Anticipation in a unique family with Charcot-Marie-Tooth syndrome and deafness: Delineation of the clinical features and review of the literature

Further evidence for a third deafness gene within the DFNA2 locus

Glypican 1 gene: Good candidate for brachydactyly type E

Kallmann syndrome in a patient with congenital spherocytosis and an interstitial 8p11.2 deletion

Molecular characterization of 22q11 deletion in a three-generation family with maternal transmission

Girl with combined cellular immunodeficiency, pancytopenia, malformations, deletion 11q23.3 → qter, and trisomy 8q24.3 → qter

Scalp defects, polythelia, microcephaly, and developmental delay: A New syndrome with apparent autosomal dominant inheritance

Novel Igα (CD79a) gene mutation in a Turkish patient with B cell-deficient agammaglobulinemia

Mosaic trisomy 8 as a cause of velopharyngeal insufficiency

Two-loci ADA haplotypes in autistic disorder

Genomic Regulatory Systems: Development and Evolution, by Eric H. Davidson

Tools

More from this journal

American Journal of Medical Genetics

Journal list menu

Tools

Follow journal

American Journal of Medical Genetics: Volume 108, Issue 4

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Vascular birthmarks of infancy: Resolving nosologic confusion

Vasculogenesis, angiogenesis, hemangiomas, and vascular malformations

Van der Woude syndrome with sensorineural hearing loss, large craniofacial sinuses, dental pulp stones, and minor limb anomalies: Report of a four-generation Thai family

Mixed clefting type in Rapp-Hodgkin syndrome

Prediction by FISH analysis of the occurrence of Wilms tumor in aniridia patients

Short bi-iliac distance in prenatal Ullrich-Turner syndrome

Anticipation in a unique family with Charcot-Marie-Tooth syndrome and deafness: Delineation of the clinical features and review of the literature

Further evidence for a third deafness gene within the DFNA2 locus

Glypican 1 gene: Good candidate for brachydactyly type E

Kallmann syndrome in a patient with congenital spherocytosis and an interstitial 8p11.2 deletion

Molecular characterization of 22q11 deletion in a three-generation family with maternal transmission

Girl with combined cellular immunodeficiency, pancytopenia, malformations, deletion 11q23.3 → qter, and trisomy 8q24.3 → qter

Scalp defects, polythelia, microcephaly, and developmental delay: A New syndrome with apparent autosomal dominant inheritance

Novel Igα (CD79a) gene mutation in a Turkish patient with B cell-deficient agammaglobulinemia

Mosaic trisomy 8 as a cause of velopharyngeal insufficiency

Two-loci ADA haplotypes in autistic disorder

Genomic Regulatory Systems: Development and Evolution, by Eric H. Davidson

Tools

More from this journal