Hannig, Vickie L.: search on Z-Library

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1

A copy number variation morbidity map of developmental delay

Cooper, Gregory M, Coe, Bradley P, Girirajan, Santhosh, Rosenfeld, Jill A, Vu, Tiffany H, Baker, Carl, Williams, Charles, Stalker, Heather, Hamid, Rizwan, Hannig, Vickie, Abdel-Hamid, Hoda, Bader, Pat

Journal:

Nature Genetics

Year:

2011

Language:

english

File:

PDF, 1.12 MB

english, 2011

2

Alopecia/mental retardation syndrome

Vickie L. Hannig, George E. Tiller

Journal:

American Journal of Medical Genetics Part A

Year:

1995

Language:

english

File:

PDF, 213 KB

english, 1995

3

Diagnostic dilemma caused by overlapping features of Prader-Willi syndrome and trisomy 18 during infancy

Holly A Ishmael, Linda M Pasztor, Paul G Rothberg, Merlin G Butler, jean Pfotenbauer, Vickie Hannig, Marshall Summar

Journal:

The Journal of Pediatrics

Year:

2000

Language:

english

File:

PDF, 638 KB

english, 2000

4

Corrigendum: A copy number variation morbidity map of developmental delay

Cooper, Gregory M, Coe, Bradley P, Girirajan, Santhosh, Rosenfeld, Jill A, Vu, Tiffany H, Baker, Carl, Williams, Charles, Stalker, Heather, Hamid, Rizwan, Hannig, Vickie, Abdel-Hamid, Hoda, Bader, Pat

Journal:

Nature Genetics

Year:

2014

Language:

english

File:

PDF, 131 KB

english, 2014

5

Book reviews

Sandra K. G. Peacock, Karen R. Eanet, Vickie Hannig

Journal:

Journal of Genetic Counseling

Year:

1996

Language:

english

File:

PDF, 450 KB

english, 1996

6

Presymptomatic testing for adult onset polycystic kidney disease in at-risk kidney transplant donors

Vickie L. Hannig, Jeanne R. Hopkins, H. Keith Johnson, John A. Phillips III, Stephen T. Reeders

Journal:

American Journal of Medical Genetics Part A

Year:

1991

Language:

english

File:

PDF, 493 KB

english, 1991

7

Maternal Cocaine Abuse and Fetal Anomalies: Evidence for Teratogenic Effects of Cocaine

HANNIG, VICKIE L., PHILLIPS, JOHN A.

Journal:

Southern Medical Journal

Year:

1991

File:

PDF, 173 KB

1991

8

A Novel SHOC2 Variant in Rasopathy

Hannig, Vickie, Jeoung, Myoungkun, Jang, Eun Ryoung, Phillips, John A., Galperin, Emilia

Journal:

Year:

2014

Language:

english

File:

PDF, 778 KB

english, 2014

9

Cerebral hemorrhage in monozygotic twins with hereditary hemorrhagic telangiectasia: case report and hemorrhagic risk evaluation

Rattani, Abbas, Dewan, Michael C., Hannig, Vickie, Naftel, Robert P., Wellons, John C., Jordan, Lori C.

Journal:

Journal of Neurosurgery Pediatrics

Year:

2017

Language:

english

File:

PDF, 2.08 MB

english, 2017

10

Utilization and evaluation of living-related donors for patients with adult polycystic kidney disease

Vickie L. Hannig, Susan M. Erickson, John A. Phillips III

Journal:

American Journal of Medical Genetics Part A

Year:

1992

Language:

english

File:

PDF, 449 KB

english, 1992

11

Whose DNA is it anyway? Relationships between families and researchers

Vickie L. Hannig, Ellen Wright Clayton, Kathryn M. Edwards

Journal:

American Journal of Medical Genetics Part A

Year:

1993

Language:

english

File:

PDF, 457 KB

english, 1993

12

Genomic imbalance in the centromeric 11p15 imprinting center in three families: Further evidence of a role for IC2 as a cause of Russell-Silver syndrome

Cytrynbaum, Cheryl, Chong, Karen, Hannig, Vickie, Choufani, Sanaa, Shuman, Cheryl, Steele, Leslie, Morgan, Thomas, Scherer, Stephen W., Stavropoulos, Dimitri J., Basran, Raveen K., Weksberg, Rosanna

Journal:

American Journal of Medical Genetics Part A

Year:

2016

Language:

english

File:

PDF, 483 KB

english, 2016

13

Speech delay and autism spectrum behaviors are frequently associated with duplication of the 7q11.23 Williams-Beuren syndrome region

Berg, Jonathan S, Brunetti-Pierri, Nicola, Peters, Sarika U, Kang, Sung-Hae L, Fong, Chin-To, Salamone, Jessica, Freedenberg, Debra, Hannig, Vickie L, Prock, Lisa Albers, Miller, David T, Raffalli, Pe

Journal:

Genetics in Medicine

Year:

2007

Language:

english

File:

PDF, 1.82 MB

english, 2007

14

Phenotypic heterogeneity of ZMPSTE24 deficiency

Cassini, Thomas A., Robertson, Amy K., Bican, Anna G., Cogan, Joy D., Hannig, Vickie L., Newman, John H., Hamid, Rizwan, Phillips, John A.

Journal:

American Journal of Medical Genetics Part A

Year:

2018

Language:

english

File:

PDF, 751 KB

english, 2018

15

What Patients and Their Relatives Think About Testing for BMPR2

Diana L. Jones, Joanne C. Sandberg, Mary J. Rosenthal, Robert C. Saunders, Vickie L. Hannig, Ellen W. Clayton

Journal:

Journal of Genetic Counseling

Year:

2008

Language:

english

File:

PDF, 136 KB

english, 2008

16

A Recurrent RNA-Splicing Mutation in the SEDL Gene Causes X-Linked Spondyloepiphyseal Dysplasia Tarda

George E. Tiller, Vickie L. Hannig, Damon Dozier, Laura Carrel, Karrie C. Trevarthen, William R. Wilcox, Stefan Mundlos, Jonathan L. Haines, Agi K. Gedeon, Jozef Gecz

Journal:

The American Journal of Human Genetics

Year:

2001

Language:

english

File:

PDF, 1.01 MB

english, 2001

17

Thirteen New Patients with Guanidinoacetate Methyltransferase Deficiency and Functional Characterization of Nineteen Novel Missense Variants in the GAMT Gene

Mercimek-Mahmutoglu, Saadet, Ndika, Joseph, Kanhai, Warsha, de Villemeur, Thierry Billette, Cheillan, David, Christensen, Ernst, Dorison, Nathalie, Hannig, Vickie, Hendriks, Yvonne, Hofstede, Floris C

Journal:

Year:

2014

Language:

english

File:

PDF, 535 KB

english, 2014

18

Limitations of exome sequencing in detecting rare and undiagnosed diseases

Burdick, Kendall J., Cogan, Joy D., Rives, Lynette C., Robertson, Amy K., Koziura, Mary E., Brokamp, Elly, Duncan, Laura, Hannig, Vickie, Pfotenhauer, Jean, Vanzo, Rena, Paul, Michael S., Bican, Anna,

Journal:

American Journal of Medical Genetics Part A

Year:

2020

Language:

english

File:

PDF, 830 KB

english, 2020

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