In five families with idiopathic (hereditary) hemochromatosis, clinical and biochemical expression of the disease occurred in offspring of probands, suggesting an autosomal dominant mode of inheritance. However, HLA typing of subjects indicated that a homozygous-heterozygous mating almost certainly had occurred in four of the five families, resulting in homozygous offspring. Thus, in these families inheritance of the hemochromatosis trait was best explained in terms of an autosomal recessive or intermediate mode of inheritance. This study demonstrates the value of HLA typing in identifying homozygous-heterozygous matings in hemochromatosis families
Hereditary hemochromatosis is a common inherited disorder of the iron metabolism. Screening studies ...
The inherited burdened is studied on diseases, associated with an overload iron in 41 children with ...
Idiopathic hemochromatosis is an underdiagnosed treatable condition inherited in an autosomal recess...
We previously reported five families with primary, genetic (idiopathic) hemochromatosis in whom HLA ...
In a study of 20 families with idiopathic hemochromatosis, relatives of probands were classified as ...
This study looks at expression of genetic hemochromatosis in the homozygous and heterozygous states....
The recently identified can didate gene, HLA-H, for haemochromatosis (HH) by Feder et al. generated ...
Studies of 73 unrelated patients and 19 families with idiopathic haemochromatosis are reported. The ...
Hereditary haemochromatosis is a common inherited disorder of iron metabolism in Caucasian populatio...
Profound advances in our knowledge of hereditary hemochromatosis (HH) during the past 150 years have...
The frequencies of different HLA-A and -B alleles in 77 Australian patients with hemochromatosis hav...
Articles free to read on publisher website Hereditary haemochromatosis (HHC) is an autosomal recessi...
A 96 member Melanesian kindred with 31 cases of iron overload is reported. Liver biopsies from 19 of...
Background & Aims: In the absence of a genetic test, diagnostic criteria for hereditary hemochromato...
Haemochromatosis (GH) is an autosomal recessive disorder in which increased iron absorption causes i...
Hereditary hemochromatosis is a common inherited disorder of the iron metabolism. Screening studies ...
The inherited burdened is studied on diseases, associated with an overload iron in 41 children with ...
Idiopathic hemochromatosis is an underdiagnosed treatable condition inherited in an autosomal recess...
We previously reported five families with primary, genetic (idiopathic) hemochromatosis in whom HLA ...
In a study of 20 families with idiopathic hemochromatosis, relatives of probands were classified as ...
This study looks at expression of genetic hemochromatosis in the homozygous and heterozygous states....
The recently identified can didate gene, HLA-H, for haemochromatosis (HH) by Feder et al. generated ...
Studies of 73 unrelated patients and 19 families with idiopathic haemochromatosis are reported. The ...
Hereditary haemochromatosis is a common inherited disorder of iron metabolism in Caucasian populatio...
Profound advances in our knowledge of hereditary hemochromatosis (HH) during the past 150 years have...
The frequencies of different HLA-A and -B alleles in 77 Australian patients with hemochromatosis hav...
Articles free to read on publisher website Hereditary haemochromatosis (HHC) is an autosomal recessi...
A 96 member Melanesian kindred with 31 cases of iron overload is reported. Liver biopsies from 19 of...
Background & Aims: In the absence of a genetic test, diagnostic criteria for hereditary hemochromato...
Haemochromatosis (GH) is an autosomal recessive disorder in which increased iron absorption causes i...
Hereditary hemochromatosis is a common inherited disorder of the iron metabolism. Screening studies ...
The inherited burdened is studied on diseases, associated with an overload iron in 41 children with ...
Idiopathic hemochromatosis is an underdiagnosed treatable condition inherited in an autosomal recess...