Familial, alternating Bell's palsy with dominant inheritance.

Familial sinus node dysfunction with autosomal dominant inheritance.

Familial gastric polyposis revisited. Autosomal dominant inheritance confirmed.

A three-generation family with idiopathic facial palsy suggesting an autosomal dominant inheritance with high penetrance.

Persistent hypermethioninaemia with dominant inheritance.

Pontobulbar palsy and neurosensory deafness (Brown-Vialetto-Van Laere syndrome) with possible autosomal dominant inheritance.

Familial urothelial cell carcinoma of the bladder with autosomal dominant inheritance and late onset phenotype.

Schwartz-Jampel syndrome with dominant inheritance.

Kniest syndrome with dominant inheritance and mucopolysacchariduria.

Neonatal primary hyperparathyroidism with autosomal dominant inheritance.

Further evidence for dominant inheritance at the chromosome 15q11-13 locus in familial Angelman syndrome.

Autosomal dominant inheritance of tetramelic monodactyly.

Autosomal dominant inheritance of Klein-Waardenburg syndrome.

Further investigations on benign myopathy with autosomal dominant inheritance.

[Centronuclear myopathy with autosomal dominant inheritance(author's transl)].

Autosomal dominant inheritance of annular pancreas.

Mendelian inheritance of familial prostate cancer.

Familial recurrent cranial nerve palsy.

Dominant familial syndromes with endocrine hyperfunction: an additional syndrome?

Familial meralgia paresthetica with an autosomal dominant trait.

Familial hyperproinsulinemia. An autosomal dominant defect.

Alarm bells for enuresis.

Alarm bells for enuresis.

Possible dominant inheritance of the idiopathic hypercalcemic syndrome.

[Dominant inheritance of pupillary pigment cysts. A follow-up study].

Suggest Documents

Familial sinus node dysfunction with autosomal dominant inheritance.

Familial gastric polyposis revisited. Autosomal dominant inheritance confirmed.

A three-generation family with idiopathic facial palsy suggesting an autosomal dominant inheritance with high penetrance.

Persistent hypermethioninaemia with dominant inheritance.

Pontobulbar palsy and neurosensory deafness (Brown-Vialetto-Van Laere syndrome) with possible autosomal dominant inheritance.

Familial urothelial cell carcinoma of the bladder with autosomal dominant inheritance and late onset phenotype.

Schwartz-Jampel syndrome with dominant inheritance.

Kniest syndrome with dominant inheritance and mucopolysacchariduria.

Neonatal primary hyperparathyroidism with autosomal dominant inheritance.

Further evidence for dominant inheritance at the chromosome 15q11-13 locus in familial Angelman syndrome.

Autosomal dominant inheritance of tetramelic monodactyly.

Autosomal dominant inheritance of Klein-Waardenburg syndrome.

Further investigations on benign myopathy with autosomal dominant inheritance.

[Centronuclear myopathy with autosomal dominant inheritance(author's transl)].

Autosomal dominant inheritance of annular pancreas.

Mendelian inheritance of familial prostate cancer.

Familial recurrent cranial nerve palsy.

Dominant familial syndromes with endocrine hyperfunction: an additional syndrome?

Familial meralgia paresthetica with an autosomal dominant trait.

Familial hyperproinsulinemia. An autosomal dominant defect.

Alarm bells for enuresis.

Alarm bells for enuresis.

Possible dominant inheritance of the idiopathic hypercalcemic syndrome.

[Dominant inheritance of pupillary pigment cysts. A follow-up study].

Familial, alternating Bell's palsy with dominant inheritance.

Recommend Documents

Follow Us