The skeletal anomalies of the hind limbs were studied on 100 youth mice +heterozygotes concerning the Dh gene (Dominant Hemimelia). The gene is dominant, not sexlinked and provokes apart from the skeletal malformations, a constant agenesia of the spleen and a microstomach. The fore limb is not affected in the heterozygotes animals. The limbs were coloured by the alizarin sulfonic acid, according to Dawson's method, and examined in pure glycerin. A study of the articulation of the instep on microscopic slides after Masson's trichromic coloration was made on animals affected by partial or total hemimelia. The greater part of the skeletal lesions may be classified into 2 groups: anomalies by excess (hyperphalangism or preaxial polydactylism) a...
Polyalanine expansion in the human HOXD13 gene induces synpolydactyly (SPD), an inherited congenital...
Polyalanine expansion in the human HOXD13 gene induces synpolydactyly (SPD), an inherited congenital...
Split hand/foot malformation type I (SHFM1) disease locus maps to chromosome 7q21.3-q22, a region th...
The genetic factors underlying human limb malformations are only beginning to be understood. An unde...
Human synpolydactyly (SPD) is an inherited congenital limb malformation caused by mutations in the H...
Cornelia de Lange Syndrome (CdLS) is characterized by a wide variety of structural and functional ab...
Purpose: Genes of the HoxD cluster play a major role in vertebrate limb development, and changes tha...
Das Verständnis der Pathogenese genetisch bedingter Malformationen konnte in den letzten Jahren ents...
Dactylaplasia, characterized by the absence of phalangeal bones in the middle digits of each foot, r...
peer reviewedA genetic analysis of biologic processes has provided substantial advances in developme...
Polyalanine expansion in the human HOXD13 gene induces synpolydactyly (SPD), an inherited congenital...
BackgroundSplit-hand/foot malformation (SHFM)-also known as ectrodactyly-is a congenital disorder ch...
Over the past ten years, the discovery and functional characterisation of murine Hox genes has led t...
The experimental and descriptive studies of the genesis of limb anomalies have revealed a great dive...
We report two patients with malformations similar to those seen in mice with the disorganization (Ds...
Polyalanine expansion in the human HOXD13 gene induces synpolydactyly (SPD), an inherited congenital...
Polyalanine expansion in the human HOXD13 gene induces synpolydactyly (SPD), an inherited congenital...
Split hand/foot malformation type I (SHFM1) disease locus maps to chromosome 7q21.3-q22, a region th...
The genetic factors underlying human limb malformations are only beginning to be understood. An unde...
Human synpolydactyly (SPD) is an inherited congenital limb malformation caused by mutations in the H...
Cornelia de Lange Syndrome (CdLS) is characterized by a wide variety of structural and functional ab...
Purpose: Genes of the HoxD cluster play a major role in vertebrate limb development, and changes tha...
Das Verständnis der Pathogenese genetisch bedingter Malformationen konnte in den letzten Jahren ents...
Dactylaplasia, characterized by the absence of phalangeal bones in the middle digits of each foot, r...
peer reviewedA genetic analysis of biologic processes has provided substantial advances in developme...
Polyalanine expansion in the human HOXD13 gene induces synpolydactyly (SPD), an inherited congenital...
BackgroundSplit-hand/foot malformation (SHFM)-also known as ectrodactyly-is a congenital disorder ch...
Over the past ten years, the discovery and functional characterisation of murine Hox genes has led t...
The experimental and descriptive studies of the genesis of limb anomalies have revealed a great dive...
We report two patients with malformations similar to those seen in mice with the disorganization (Ds...
Polyalanine expansion in the human HOXD13 gene induces synpolydactyly (SPD), an inherited congenital...
Polyalanine expansion in the human HOXD13 gene induces synpolydactyly (SPD), an inherited congenital...
Split hand/foot malformation type I (SHFM1) disease locus maps to chromosome 7q21.3-q22, a region th...