WULFSBERG, ERIC A.: search on Z-Library

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1

Confirmation of the catania brachydactylous type of acrofacial dysostosis: Report of a second family

Wulfsberg, Eric A., Campbell, Andrew B., Lurie, Iosif W., Eanet, Karen R.

Journal:

American Journal of Medical Genetics

Year:

1996

File:

PDF, 378 KB

1996

2

A Complex Chromosome Rearrangement in a Boy with Autism

LOPREIATO, JOSEPH O., WULFSBERG, ERIC A.

Journal:

Journal of Developmental & Behavioral Pediatrics

Year:

1992

File:

PDF, 451 KB

1992

3

“Holoprosencephaly-polydactyly” (pseudotrisomy 13) syndrome: Expansion of the phenotypic spectrum

Iosif W. Lurie, Eric A. Wulfsberg

Journal:

American Journal of Medical Genetics Part A

Year:

1993

Language:

english

File:

PDF, 483 KB

english, 1993

4

Policy Statement: American college of medical genetics. Fragile X Syndrome: Diagnostic and carrier testing

Vicki Park, Patricia Howard-Peebles, Stephanie Sherman, Annette Taylor, Eric Wulfsberg

Journal:

American Journal of Medical Genetics Part A

Year:

1994

Language:

english

File:

PDF, 227 KB

english, 1994

5

Chondrodysplasia punctata: A boy with X-linked recessive chondrodysplasia punctata due to an inherited X-Y translocation with a current classification of these disorders

Eric A. Wulfsberg, Jerri Curtis, Carol H. Jayne

Journal:

American Journal of Medical Genetics Part A

Year:

1992

Language:

english

File:

PDF, 755 KB

english, 1992

6

Chromosome 10qter deletion syndrome: A review and report of three new cases

Dr. Eric A. Wulfsberg, Ramona P. Weaver, Christopher M. Cunniff, Marilyn C. Jones, Kenneth Lyons Jones

Journal:

American Journal of Medical Genetics Part A

Year:

1989

Language:

english

File:

PDF, 395 KB

english, 1989

7

Familial testicular germ cell tumor: no associated syndromic pattern identified

Mueller, Christine M, Korde, Larissa A, McMaster, Mary L, Peters, June A, Bratslavsky, Gennady, Watkins, Rissah J, Ling, Alex, Kratz, Christian P, Wulfsberg, Eric A, Rosenberg, Philip S, Greene, Mark

Journal:

Hereditary Cancer in Clinical Practice

Year:

2014

Language:

english

File:

PDF, 193 KB

english, 2014

8

Reply to “What's in a name? The 22q11.2 deletion”

Wulfsberg, Eric A., Leana-Cox, Julie, Neri, Giovanni

Journal:

American Journal of Medical Genetics

Year:

1997

Language:

english

File:

PDF, 18 KB

english, 1997

9

Antenatal diagnosis of lethal skeletal dysplasias

Tretter, Anne E., Saunders, Roger C., Meyers, Carol M., Dungan, Jeffrey S., Grumbach, Kathryn, Sun, Chen-Chih J., Campbell, Andrew B., Wulfsberg, Eric A.

Journal:

American Journal of Medical Genetics

Year:

1998

Language:

english

File:

PDF, 60 KB

english, 1998

10

Familial DiGeorge/velocardiofacial syndrome with deletions of chromosome area22q11.2: Report of five families with a review of the literature

Leana-Cox, Julie, Pangkanon, Suthipong, Eanet, Karen R., Curtin, Martha S., Wulfsberg, Eric A.

Journal:

American Journal of Medical Genetics

Year:

1996

Language:

english

File:

PDF, 754 KB

english, 1996

11

Vertebral hypersegmentation in a case of the VATER association

M.D. Eric A. Wulfsberg, Terri L. Phillips-Dawkins, Ronald L. Thomas

Journal:

American Journal of Medical Genetics Part A

Year:

1992

Language:

english

File:

PDF, 500 KB

english, 1992

12

Human PRRX1 and PRRX2 genes: cloning, expression, genomic localization, and exclusion as disease genes for Nager syndrome

Russell A. Norris, Karen K. Scott, Clara S. Moore, Gail Stetten, Cuyler R. Brown, Ethylin Wang Jabs, Eric A. Wulfsberg, Jack Yu, Michael J. Kern

Journal:

Mammalian Genome

Year:

2000

Language:

english

File:

PDF, 315 KB

english, 2000

13

What's in a name? chromosome 22q abnormalities and the DiGeorge, velocardiofacial, and conotruncal anomalies face syndromes

Wulfsberg, Eric A., Leana-Cox, Julie, Neri, Giovanni

Journal:

American Journal of Medical Genetics

Year:

1996

Language:

english

File:

PDF, 355 KB

english, 1996

14

High resolution chromosome banding in the Rubinstein—Taybi syndrome

Eric A. Wulfsberg, Ivana J. Klisak, Robert S. Sparkes

Journal:

Clinical Genetics

Year:

1983

Language:

english

File:

PDF, 223 KB

english, 1983

15

The inheritance of conotruncal malformations: a review and report of two siblings with tetralogy of Fallot with pulmonary atresia

Eric A. Wulfsberg, Eric J. Zintz, John W. Moore

Journal:

Clinical Genetics

Year:

1991

Language:

english

File:

PDF, 368 KB

english, 1991

16

TCOF1 mutations excluded from a role in other first and second branchial arch-related disorders

Alessandra Splendore, Maria Rita Passos-Bueno, Ethylin Wang Jabs, Lionel Van Maldergem, Eric A. Wulfsberg

Journal:

American Journal of Medical Genetics Part A

Year:

2002

Language:

english

File:

PDF, 45 KB

english, 2002

17

Autosomal dominant tetramelic postaxial oligodactyly

Eric A. Wulfsberg, Laura J. Mirkinson, Steven J. Meister

Journal:

American Journal of Medical Genetics Part A

Year:

1993

Language:

english

File:

PDF, 513 KB

english, 1993

18

A 15 → 1 translocation in a patient mosaic for presence or absence of an isodic(15p)(q11)

Eric A. Wulfsberg, Dr. Robert S. Sparkes, Ivana J. Klisak, William B. Gurfield, John M. Opitz

Journal:

American Journal of Medical Genetics Part A

Year:

1982

Language:

english

File:

PDF, 254 KB

english, 1982

19

Speech characteristics in the Kabuki syndrome

Sheila Upton, Carmella S. Stadter, Pat Landis, Eric A. Wulfsberg

Journal:

American Journal of Medical Genetics Part A

Year:

2003

Language:

english

File:

PDF, 158 KB

english, 2003

20

SPIE Proceedings [SPIE Fourth International Symposium on laser Precision Microfabrication - Munich, Germany (Saturday 21 June 2003)] Fourth International Symposium on Laser Precision Microfabrication - Sapphire tools for laser-assisted microforming

Wulfsberg, Jens P., Hilpert, Sven-Eric, Ostendorf, Andreas, Kulik, Christian J., Temme, Thorsten, Samm, Katja, Miyamoto, Isamu, Ostendorf, Andreas, Sugioka, Koji, Helvajian, Henry

Year:

2003

Language:

english

File:

PDF, 561 KB

english, 2003

21

Trisomy 18 mosaicism: Clues to the diagnosis

Harold N. Bass, Michelle Fox, Eric Wulfsberg, Robert S. Sparkes, BarbaraF Crandall

Journal:

Clinical Genetics

Year:

1982

Language:

english

File:

PDF, 318 KB

english, 1982

22

Acrofacial dysostosis with ambiguous genitalia

Eric A. Wulfsberg, Jerri Curtis, Thomas E. Wiswell, Robert A. Puntel, Sondra W. Levin

Journal:

American Journal of Medical Genetics Part A

Year:

1990

Language:

english

File:

PDF, 493 KB

english, 1990

23

Gorlin syndrome (naevoid basal cell carcinoma syndrome): Prenatal detection in a fetus with macrocephaly and ventriculomegaly

W. Allen Hogge, Carol Blank, Linda B. Roochvarg, Joan S. Hogge, Eric A. Wulfsberg, Leslie J. Raffel

Journal:

Prenatal Diagnosis

Year:

1994

Language:

english

File:

PDF, 268 KB

english, 1994

24

Evidence for an association between markers on chromosome 19q and non-syndromic cleft lip with or without cleft palate in two groups of multiplex families

D. F. Wyszynski, Nancy Maestri, Iain McIntosh, E. Anne Smith, Amy F. Lewanda, Constanza Garcia-Delgado, Enrique Vinageras-Guarneros, Eric Wulfsberg, Terri H. Beaty

Journal:

Year:

1996

Language:

english

File:

PDF, 33 KB

english, 1996

25

Complex chromosomal rearrangements: some breakpoints may have cellular adaptive significance

Iosif W. Lurie, Eric A. Wulfsberg, Gayathri Prabhakar, Lynne S. Rosenblum-Vos, Karen R. Supovitz, Maimon M. Cohen

Journal:

Clinical Genetics

Year:

1994

Language:

english

File:

PDF, 397 KB

english, 1994

26

Monozygotic twin girls with diploid/triploid chromosome mosaicism and cutaneous pigmentary dysplasia

Eric A. Wulfsberg, William C. Wassel, Cynthia A. Polo

Journal:

Clinical Genetics

Year:

1991

Language:

english

File:

PDF, 453 KB

english, 1991

27

No Evidence of Linkage for Cleft Lip with or without Cleft Palate to a Marker Near the Transforming Growth Factor Alpha Locus in Two Populations

Wyszynski, Diego F., Maestri, Nancy, Lewanda, Amy F., McIntosh, Iain, Smith, Anne, Garc&iacute, a-Delgado, Constanza, Vinageras-Guarneros, Enrique, Wulfsberg, Eric, Beaty, Terri H.

Journal:

Year:

1997

Language:

english

File:

PDF, 1.21 MB

english, 1997

28

Is the autosomal dominant Opitz GBBB syndrome part of the DiGeorge/velocardiofacial syndrome with deletions of chromosome area 22q11.2?

Eric A. Wulfsberg

Journal:

American Journal of Medical Genetics Part A

Year:

1996

Language:

english

File:

PDF, 217 KB

english, 1996

29

On the nosology of the “Schinzel-phocomelia” and “Al-Awadi/Raas-Rothschield” syndromes

Iosif W. Lurie, Eric A. Wulfsberg

Journal:

American Journal of Medical Genetics Part A

Year:

1993

Language:

english

File:

PDF, 88 KB

english, 1993

30

Rokitansky sequence in association with the facio-auriculo-vertebral sequence: Part of a mesodermal malformation spectrum?

Eric A. Wulfsberg, Tamara M. Grigbsy

Journal:

American Journal of Medical Genetics Part A

Year:

1990

Language:

english

File:

PDF, 370 KB

english, 1990

31

Third Prader-Willi syndrome phenotype due to maternal uniparental disomy 15 with mosaic trisomy 15

Erika Olander, Judith Stamberg, Lisa Steinberg, Eric A. Wulfsberg

Journal:

American Journal of Medical Genetics Part A

Year:

2000

Language:

english

File:

PDF, 85 KB

english, 2000

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