Iosif W. Lurie: search on Z-Library

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1

Atrioventricular septal defects: Possible etiologic differences between complete and partial defects

Christopher A. Loffredo, Jeffrey Hirata, P. David Wilson, Charlotte Ferencz, Iosif W. Lurie

Journal:

Birth Defects Research Part A: Clinical and Molecular Teratology

Year:

2001

Language:

english

File:

PDF, 108 KB

english, 2001

2

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

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

“Shifted” threshold may explain diversity of cardiovascular malformations in multiple congenital abnormalities syndromes: 3C (Ritscher-Schinzel) syndrome as an example

Lurie, Iosif W., Ferencz, Charlotte

Journal:

American Journal of Medical Genetics

Year:

1996

Language:

english

File:

PDF, 310 KB

english, 1996

5

VACTERL-hydrocephaly, DK-phocomelia, and cerebro-cardio-radio-reno-rectal community

Lurie, Iosif W., Ferencz, Charlotte

Journal:

American Journal of Medical Genetics

Year:

1997

Language:

english

File:

PDF, 137 KB

english, 1997

6

Congenital anomalies of the ear, nose, and throat

Lurie, Iosif W.

Journal:

American Journal of Medical Genetics

Year:

1999

Language:

english

File:

PDF, 23 KB

english, 1999

7

Interrupted aortic arch: An epidemiologic study

Loffredo, Christopher A., Ferencz, Charlotte, Wilson, P. David, Lurie, Iosif W.

Journal:

Year:

2000

Language:

english

File:

PDF, 79 KB

english, 2000

8

The Neu-Laxova syndrome—a distinct entity

Professor Gennady I. Lazjuk, Iosif W. Lurie, Teresa I. Ostrowskaja, Eugeny D. Cherstvoy, Irena A. Kirillova, Michael K. Nedzved, Sergei S. Usoev, John M. Optiz

Journal:

American Journal of Medical Genetics Part A

Year:

1979

Language:

english

File:

PDF, 428 KB

english, 1979

9

Aprosencephaly-atelencephaly and the aprosencephaly (XK) syndrome

Dr. Iosif W. Lurie, Michael K. Nedzved, Gennady I. Lazjuk, Irena A. Kirillova, Eugeny D. Cherstvoy, John M. Optiz

Journal:

American Journal of Medical Genetics Part A

Year:

1979

Language:

english

File:

PDF, 498 KB

english, 1979

10

The XK-aprosencephaly syndrome

Iosif W. Lurie, Michael K. Nedzed, Gennady I. Lazjuk, Irena A. Kirillova, Eugeny D. Cherstvoy, Teresa I. Ostrovskaja, Ivan A. Shved

Journal:

American Journal of Medical Genetics Part A

Year:

1980

Language:

english

File:

PDF, 249 KB

english, 1980

11

Letter to the editor: Familial omphalocele and recurrence risk

Iosif W. Lurie, Helena G. Ilyina, John M. Opitz

Journal:

American Journal of Medical Genetics Part A

Year:

1984

Language:

english

File:

PDF, 157 KB

english, 1984

12

Meckel syndrome in different populations

Dr. Iosif W. Lurie, Alexander N. Prytkov, Lyudmila V. Meldere, John M. Opitz, James F. Reynolds

Journal:

American Journal of Medical Genetics Part A

Year:

1984

Language:

english

File:

PDF, 512 KB

english, 1984

13

Gollop–Wolfgang complex in a 3-month-old girl

Iosif W. Lurie, Helena G. Ilyina, John M. Opitz, James F. Reynolds

Journal:

American Journal of Medical Genetics Part A

Year:

1986

Language:

english

File:

PDF, 193 KB

english, 1986

14

Dubowitz syndrome: Possible evidence for a clinical subtype

Dr. Helena G. Ilyina, Iosif W. Lurie

Journal:

American Journal of Medical Genetics Part A

Year:

1990

Language:

english

File:

PDF, 456 KB

english, 1990

15

11Q;22Q translocation: Third case of imbalance not due to 3:1 nondisjunction in first meiosis

Iosif W. Lurie, Ljubov V. Podleschuk

Journal:

American Journal of Medical Genetics Part A

Year:

1992

Language:

english

File:

PDF, 70 KB

english, 1992

16

Unusual complex of congenital malformations

Tatjana Zolotukhina, Michail Kuznetsov, Dr. Iosif Lurie, Helena Ilyina

Journal:

American Journal of Medical Genetics Part A

Year:

1993

Language:

english

File:

PDF, 207 KB

english, 1993

17

Autosomal imbalance syndromes: Genetic interactions and the origin of congenital malformations in aneuploidy syndromes

Journal:

American Journal of Medical Genetics Part A

Year:

1993

Language:

english

File:

PDF, 726 KB

english, 1993

18

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

19

Further delineation of the Beemer–Langer syndrome using concordance rates in affected sibs

Journal:

American Journal of Medical Genetics Part A

Year:

1994

Language:

english

File:

PDF, 402 KB

english, 1994

20

Genetics of the Costello syndrome

Journal:

American Journal of Medical Genetics Part A

Year:

1994

Language:

english

File:

PDF, 204 KB

english, 1994

21

Trisomy 7p resulting from isochromosome formation and whole-arm translocation

Iosif W. Lurie, Marcia F. Schwartz, Stuart Schwartz, Maimon M. Cohen

Journal:

American Journal of Medical Genetics Part A

Year:

1995

Language:

english

File:

PDF, 526 KB

english, 1995

22

Trisomy 2p: Analysis of unusual phenotypic findings

Dr. Iosif W. Lurie, Helena G. Ilyina, Dora B. Gurevich, Natalja V. Rumyantseva, Irena V. Naumchik, Claudio Castellan, Adelheid Hoeller, Albert Schinzel

Journal:

American Journal of Medical Genetics Part A

Year:

1995

Language:

english

File:

PDF, 856 KB

english, 1995

23

Further delineation of the branchio-oculo-facial syndrome

Angela E. Lin, Robert J. Gorlin, Iosif W. Lurie, Han G. Brunner, Ineke van der Burgt, Irena V. Naumchik, Natalja V. Rumyantseva, Sabine Stengel-Rutkowski, Kenneth Rosenbaum, Peter Meinecke, Dietmar Mu

Journal:

American Journal of Medical Genetics Part A

Year:

1995

Language:

english

File:

PDF, 1.73 MB

english, 1995

24

Kabuki make-up (Niikawa-Kuroki) syndrome in the Byelorussian register of congenital malformations: Ten new observations

Helena Ilyina, Iosif Lurie, Irena Naumtchik, Dmitry Amoashy, Galina Stephanenko, Valery Fedotov, Albina Kostjuk

Journal:

American Journal of Medical Genetics Part A

Year:

1995

Language:

english

File:

PDF, 554 KB

english, 1995

25

Further study of genetic interactions: Loss of short arm material in patients with ring chromosome 4 changes developmental pattern of del(4)(q33)

Journal:

American Journal of Medical Genetics Part A

Year:

1995

Language:

english

File:

PDF, 381 KB

english, 1995

26

Phenotypic mapping and clinical ideology

Iosif W. Lurie, John M. Opitz

Journal:

American Journal of Medical Genetics Part A

Year:

1995

Language:

english

File:

PDF, 139 KB

english, 1995

27

Partial trisomy 4q and preaxial limb defects

Journal:

American Journal of Medical Genetics Part A

Year:

2005

Language:

english

File:

PDF, 38 KB

english, 2005

28

Kidney abnormalities in persons with monosomy 15q26

Journal:

American Journal of Medical Genetics Part A

Year:

2008

Language:

english

File:

PDF, 52 KB

english, 2008

29

Chromosomal map of human brain malformations

Nataliya Tyshchenko, Iosif Lurie, Albert Schinzel

Journal:

Year:

2008

Language:

english

File:

PDF, 296 KB

english, 2008

30

Phenotypic spectrum of tetrasomy 12p and prenatal counseling: potential underestimation of severity

Iosif W. Lurie M.D.

Journal:

Clinical Genetics

Year:

1998

Language:

english

File:

PDF, 160 KB

english, 1998

31

4q32–q35 and 6q16–q22 are valuable candidate regions for split hand/foot malformation

Lurie, Iosif W, Schinzel, Albert, Niedrist, Dunja

Journal:

European Journal of Human Genetics

Year:

2009

Language:

english

File:

PDF, 103 KB

english, 2009

32

Distal trisomy 10q and limb defects

Journal:

Annales de Génétique

Year:

2002

Language:

english

File:

PDF, 44 KB

english, 2002

33

Two simultaneous terminal deletions in the same patient: a one—vs two-hit origin

Iosif W. Lurie, Maimon M. Cohen

Journal:

Clinical Genetics

Year:

1993

Language:

english

File:

PDF, 116 KB

english, 1993

34

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

35

Structural autosomal imbalance and oesophageal defects: Addendum to the article by Felix et al. (2007)

Journal:

European Journal of Medical Genetics

Year:

2007

Language:

english

File:

PDF, 80 KB

english, 2007

36

Heart disease in infancy: A window to the world of fetal cardiology

Lurie, Iosif W., Ferencz, Charlotte, Brenner, Joel I.

Journal:

Progress in Pediatric Cardiology

Year:

1996

Language:

english

File:

PDF, 577 KB

english, 1996

37

Unbalanced Translocations Involving Chromosome Region 10q25.3q26.3 in Patients with Intellectual Disability and Complex Phenotypes

Hryshchenko, Nataliya V., Bychkova, Ganna M., Tavokina, Lyubov V., Brovko, Anton O., Graziano, Claudio, Soloviov, Oleksandr O., Hettinger, Joe A., Patsalis, Philippos C., Lurie, Iosif W., Livshits, Lu

Journal:

Cytogenetic and Genome Research

Year:

2015

Language:

english

File:

PDF, 372 KB

english, 2015

38

Uniparental disomy 7 in Silver—Russell syndrome and primordial growth retardation

Kotzot, Dieter, Schmitt, Silke, Bernasconi, Fabiana, Robinson, Wendy P., Lurie, Iosif W., Ilyina, Helena, Méhes, Károly, Hamel, Ben C.J., Otten, Barto J., Hergersberg, Martin, Werder, Edmond, Schoenle

Journal:

Human Molecular Genetics

Year:

1995

Language:

english

File:

PDF, 2.19 MB

english, 1995

39

Clinical Manifestations of Partial Trisomy 2p

Lurie, Iosif W.

Journal:

Cytogenetic and Genome Research

Year:

2014

Language:

english

File:

PDF, 67 KB

english, 2014

40

A novel interstitial deletion of 2q22.3 q23.3 in a patient with dysmorphic features, epilepsy, aganglionosis, pure red cell aplasia, and skeletal malformations

Bravo-Oro, Antonio, Lurie, Iosif W., Elizondo-Cárdenas, Gabriela, Peña-Zepeda, Claudia, Salazar-Martínez, Abel, Correa-González, Cecilia, Castrillo, José Luis, Avila, Silvia, Esmer, Carmen

Journal:

American Journal of Medical Genetics Part A

Year:

2015

Language:

english

File:

PDF, 2.69 MB

english, 2015

41

A critical region for ulnar defects in patients with 4q deletions may be narrowed

Lurie, Iosif W.

Journal:

Clinical Dysmorphology

Year:

2016

Language:

english

File:

PDF, 55 KB

english, 2016

42

Distal trisomy 3q as a risk factor for neural tube defects

Journal:

Taiwanese Journal of Obstetrics and Gynecology

Year:

2016

Language:

english

File:

PDF, 162 KB

english, 2016