<p>Arrows show the probands in each family. Genetic findings for each individual tested are noted in the pedigree.</p
<p>High clinical variability was observed even within the same family. Not all affected persons mani...
<p>Clinical features and gene identification results of the probands and their first relatives.</p
<p>A) Pedigree for a family with the <i>PSEN1 A79V</i> mutation. B) Pedigree for a family with the <...
<p>Clinical features of affected family members associated with <i>WFS1</i> mutations found in this ...
<p>*M, male; F, female; DM, diabetes mellitus; OA, optic atrophy; D, deafness; DI, diabetes insipidu...
<p>Black symbols indicate clinically affected family members, open symbols indicate unaffected, and ...
<p>Below the individuals, genotypes are presented for either p.S1653KfsX2 (M1), p.L2784R (M2), p.Y29...
<p>The pedigrees and automated sequencing traces of the <i>WISP3</i> gene mutations in the two famil...
*<p>: In the genotypes of children, alleles with the mutation were denoted in boldface.</p
(A) Pedigree of three consanguineous families studied. Black boxes indicated affected individuals. R...
<p>*Novel mutations are indicated in boldface.</p>§<p>Individual with detectable <i>WFS1</i> mutatio...
<p><b>A<sup>I</sup></b>, Pedigree of the Qatari family carrying the p.*2625Gluext*11 mutation in <i>...
<p>Pedigrees (Ped) of the six Saudi Arabian families (F1-6) are represented in the same order as in ...
<p><b>A:</b> Pedigree and disease-haplotype segregation of family A. Blackened symbols represent aff...
<p>This pedigree represents the family history of cancer in patient number 3. The proband, or origin...
<p>High clinical variability was observed even within the same family. Not all affected persons mani...
<p>Clinical features and gene identification results of the probands and their first relatives.</p
<p>A) Pedigree for a family with the <i>PSEN1 A79V</i> mutation. B) Pedigree for a family with the <...
<p>Clinical features of affected family members associated with <i>WFS1</i> mutations found in this ...
<p>*M, male; F, female; DM, diabetes mellitus; OA, optic atrophy; D, deafness; DI, diabetes insipidu...
<p>Black symbols indicate clinically affected family members, open symbols indicate unaffected, and ...
<p>Below the individuals, genotypes are presented for either p.S1653KfsX2 (M1), p.L2784R (M2), p.Y29...
<p>The pedigrees and automated sequencing traces of the <i>WISP3</i> gene mutations in the two famil...
*<p>: In the genotypes of children, alleles with the mutation were denoted in boldface.</p
(A) Pedigree of three consanguineous families studied. Black boxes indicated affected individuals. R...
<p>*Novel mutations are indicated in boldface.</p>§<p>Individual with detectable <i>WFS1</i> mutatio...
<p><b>A<sup>I</sup></b>, Pedigree of the Qatari family carrying the p.*2625Gluext*11 mutation in <i>...
<p>Pedigrees (Ped) of the six Saudi Arabian families (F1-6) are represented in the same order as in ...
<p><b>A:</b> Pedigree and disease-haplotype segregation of family A. Blackened symbols represent aff...
<p>This pedigree represents the family history of cancer in patient number 3. The proband, or origin...
<p>High clinical variability was observed even within the same family. Not all affected persons mani...
<p>Clinical features and gene identification results of the probands and their first relatives.</p
<p>A) Pedigree for a family with the <i>PSEN1 A79V</i> mutation. B) Pedigree for a family with the <...