Kukolich, Mary K.: search on Z-Library

The world's largest scientific articles store. 70,000,000+ articles for free.

1

Clinical delineation of the PACS1 -related syndrome-Report on 19 patients

Schuurs-Hoeijmakers, Janneke H. M., Landsverk, Megan L., Foulds, Nicola, Kukolich, Mary K., Gavrilova, Ralitza H., Greville-Heygate, Stephanie, Hanson-Kahn, Andrea, Bernstein, Jonathan A., Glass, Jenn

Journal:

American Journal of Medical Genetics Part A

Year:

2016

Language:

english

File:

PDF, 475 KB

english, 2016

2

Ring chromosome 8 syndrome: Further characterization

Tonk, Vijay S., Kukolich, Mary K., Morgan, David, Khan, Ashraf, Jalal, Syed M.

Journal:

American Journal of Medical Genetics

Year:

2000

Language:

english

File:

PDF, 633 KB

english, 2000

3

Euchromatic 9q+ heteromorphism in a family

S. M. Jalal, Mary K. Kukolich, Mary Garcia, Donald W. Day

Journal:

American Journal of Medical Genetics Part A

Year:

1990

Language:

english

File:

PDF, 142 KB

english, 1990

4

Direct chromosome analysis from neonatal cord blood

Dr. Donald W. Day, S. M. Jalal, Leslie Sinclair-Worley, Mary Kukolich, Mahlon Freeman, Joseph Sakakini, John M. Opitz, James F. Reynolds

Journal:

American Journal of Medical Genetics Part A

Year:

1988

Language:

english

File:

PDF, 211 KB

english, 1988

5

Prenatal diagnosis of a de novo trisomy 6q22.2→6qter and monosomy lpter→1p36.3. Case report with a 2-year follow-up and a brief review of other prenatal cases of partial trisomy 6q

Anita S. Kulharya, Mary E. Carlin, William A. Stettler, Martine Huslig, Mary K. Kukolich, Jaime Garcia-Heras

Journal:

Clinical Genetics

Year:

1997

Language:

english

File:

PDF, 579 KB

english, 1997

6

Euchromatic 16p + heteromorphism: First report in North America

S. M. Jalal, Nancy R. Schneider, Mary K. Kukolich, Golder N. Wilson

Journal:

American Journal of Medical Genetics Part A

Year:

1990

Language:

english

File:

PDF, 257 KB

english, 1990

7

Tetrasomy 9p: an emerging syndrome

S. M. Jalal, Mary K. Kukolich, Mary Garcia, Toni R. Benjamin, Donald W. Day

Journal:

Clinical Genetics

Year:

1991

Language:

english

File:

PDF, 387 KB

english, 1991

8

ARTERIAL OCCLUSION IN 47,XYY MALE

Kukolich, Mary, Hall, JudithG.

Journal:

Year:

1975

Language:

english

File:

PDF, 164 KB

english, 1975

9

Partial deletion 10q

Raymond C. Lewandowski, Mary K. Kukolich, Joseph W. Sears, Carl B. Mankinen

Journal:

Year:

1978

Language:

english

File:

PDF, 203 KB

english, 1978

10

Interstitial deletions 4q21.1q25 and 4q25q27: Phenotypic variability and relation to Rieger anomaly

Anita S. Kulharya, Mark Maberry, Mary K. Kukolich, Donald W. Day, Nancy R. Schneider, Golder N. Wilson, Dr. Vijay Tonk

Journal:

American Journal of Medical Genetics Part A

Year:

1995

Language:

english

File:

PDF, 495 KB

english, 1995

11

Duplication of chromosome band 12q24.11q24.23 results in apparent Noonan syndrome

Oleg A. Shchelochkov, Ankita Patel, George M. Weissenberger, A. Craig Chinault, Joanna Wiszniewska, Priscilla H. Fernandes, Christine Eng, Mary K. Kukolich, V. Reid Sutton

Journal:

American Journal of Medical Genetics Part A

Year:

2008

Language:

english

File:

PDF, 199 KB

english, 2008

12

Sensenbrenner syndrome (Cranioectodermal dysplasia): Clinical and molecular analyses of 39 patients including two new patients

Lin, Angela E., Traum, Avram Z., Sahai, Inderneel, Keppler-Noreuil, Kim, Kukolich, Mary K., Adam, Margaret P., Westra, Sjirk J., Arts, Heleen H.

Journal:

American Journal of Medical Genetics Part A

Year:

2013

Language:

english

File:

PDF, 1.97 MB

english, 2013

13

De novo partial duplications 1p: Report of two new cases and review

Garcia-Heras, Jaime, Corley, Norlela, Garcia, Mary F., Kukolich, Mary K., Smith, Kim G., Day, Donald W.

Journal:

American Journal of Medical Genetics

Year:

1999

Language:

english

File:

PDF, 86 KB

english, 1999

14

Tetraploidy: A report of three live-born infants

Dr. Paula R. Scarbrough, Joseph Hersh, Mary K. Kukolich, Andrew J. Carroll, Sara C. Finley, Richard Hochberger, Shirley Wilkerson, F. F. Yen, Becky W. Althaus

Journal:

American Journal of Medical Genetics Part A

Year:

1984

Language:

english

File:

PDF, 623 KB

english, 1984

15

Endocardial fibroelastosis, neurologic dysfunction and unusual facial appearance in two brothers, coincidentally associated with dominantly inherited macrocephaly

Mark T. Jennings, Judith G. Hall, Mary Kukolich

Journal:

American Journal of Medical Genetics Part A

Year:

1980

Language:

english

File:

PDF, 387 KB

english, 1980

16

Mutation Analysis of UBE3A in Angelman Syndrome Patients

Perrine Malzac, Hayley Webber, Anne Moncla, John M. Graham Jr, Mary Kukolich, Charles Williams, Roberta A. Pagon, Linda A. Ramsdell, Tatsuya Kishino, Joseph Wagstaff

Journal:

The American Journal of Human Genetics

Year:

1998

Language:

english

File:

PDF, 273 KB

english, 1998

17

Functional variants in TBX2 are associated with a syndromic cardiovascular and skeletal developmental disorder

Liu, Ning, Schoch, Kelly, Luo, Xi, Pena, Loren, Bhavana, Venkata Hemanjani, Kukolich, Mary K, Stringer, Sarah, Powis, Zöe, Radtke, Kelly, Mroske, Cameron, Deak, Kristen, McDonald, Marie T, McConkie-Ro

Journal:

Human Molecular Genetics

Year:

2018

Language:

english

File:

PDF, 2.15 MB

english, 2018

18

Mild phenotypic effects of a de novo deletion Xpter→Xp22.3 and duplication 3pter→3p23

Anita S. Kulharya, Heidi Roop, Mary K. Kukolich, Ronald G. Nachtman, John W. Belmont, Dr. Jaime Garcia-Heras

Journal:

American Journal of Medical Genetics Part A

Year:

1995

Language:

english

File:

PDF, 592 KB

english, 1995

19

Trisomy 22: No longer an enigma

Mary K. Kukolich, Anita Kulharya, S. M. Jalal, Margaret Drummond-Borg

Journal:

American Journal of Medical Genetics Part A

Year:

1989

Language:

english

File:

PDF, 321 KB

english, 1989

To build up a library is to create a life. It’s never just a random collection of books.

— Carlos María Domínguez

Official channel

Z-Library Desktop Launcher

Z-Library Since 2009 support@1delivery.pm

EnglishРусскийEspañolItalianoελληνικάاللغة العربيةBahasa IndonesiaBahasa Malaysiaहिन्दीDeutschFrançaisPortuguêsУкраїнськаPolski中文繁體中文日本語Tiếng ViệtAzərbaycan DiliՀայոց լեզուภาษาไทยTürk Diliქართველიবাংলাپښتوతెలుగుاردو한국어SrpskiБългарски