NIGMS Collection - Extended Families

Coriell Institute for Medical Research

NIGMS Repository Extended Families

The following table lists families which have been identified as being suitable for linkage studies. Each family contains samples from at least four children and both parents.

Adenomatous Polyposis of the Colon - Family 967 (pedigree available)
Amish Major Affective Disorders - Family 210

Amish Major Affective Disorders - Family 310

Amish Major Affective Disorders - Family 410

Amish Major Affective Disorders - Family 884-110
Left

Core

Right

Ataxia Telangiectasia - Family 516 (pedigree available)
Ataxia Telangiectasia - Family 605 (pedigree available)
Cystic Fibrosis - Family 1038 (pedigree available)
Cystic Fibrosis - Family 1047 (pedigree available)
Cystic Fibrosis - Family 1064 (pedigree available)
Cystic Fibrosis - Family 1078 (pedigree available)
Cystic Fibrosis - Family 1080 (pedigree available)
Diabetes Mellitus: Juvenile Onset - Family 243 (pedigree available)
Diabetes Mellitus: Juvenile Onset - Family 620 (pedigree available)
Diabetes Mellitus: Maturity Onset Diabetes - Family 95

Diabetes Mellitus and Insipidus with Optic Atrophy and Deafness - Family 1157 (pedigree available)
Dysautonomia, Familial - Family 810 (pedigree available)
Dysautonomia, Familial - Family 816 (pedigree available)
Fragile X Mental Retardation - Family 971 (pedigree available) Huntington Disease - Family 690
Huntington Disease - Family 691
Huntington Disease - Family 692

Manic Depressive Psychosis - Family 811 (pedigree available)
Manic Depressive Psychosis - Family 823 (pedigree available)
(pedigree available)
Marfan Syndrome - Family 1216 (pedigree available)
Multiple Sclerosis - Family 2112 (pedigree available)
Retinitis Pigmentosa-1 - Family 2110
Retinitis Pigmentosa-1 - Family 2111
Tuberous Sclerosis - Family 1036 (pedigree available)
Usher Syndrome, Type I - Family 1187 (pedigree available)
Usher Syndrome, Type I - Family 2116 (pedigree available)
Usher Syndrome, Type I - Family 2117 (pedigree available)
Usher Syndrome, Type I - Family 2166 (pedigree available)
Usher Syndrome, Type II - Family 2114 (pedigree available)

Our mission is to prevent and cure disease through biomedical research.

CUSTOMER SERVICE
customerservice@coriell.org (800) 752-3805 • (856) 757-4848

Coriell Institute for Medical Research
403 Haddon Avenue Camden, NJ 08103, USA (856) 966-7377