I. Lurie

发表

Genetics of the Costello syndrome.

I. Lurie, I. W. Lurie, 1994, American journal of medical genetics.

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

A. Schinzel, D. Niedrist, I. Lurie, 2009, European Journal of Human Genetics.

Chromosomal map of human brain malformations

A. Schinzel, I. Lurie, N. Tyshchenko, 2008, Human Genetics.

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

I. Lurie, 1993, American journal of medical genetics.

The malformations of the urinary system in autosomal disorders

G. Lazjuk, I. Lurie, G. I. Kravtzova, 1975, Virchows Archiv A.

Epigenetic mutations of the imprinted IGF2-H19 domain in Silver–Russell syndrome (SRS): results from a large cohort of patients with SRS and SRS-like phenotypes

H. Kayserili, K. Chrzanowska, K. Õunap, 2008, Journal of Medical Genetics.

Atrioventricular septal defects: possible etiologic differences between complete and partial defects.

C. Loffredo, C. Ferencz, P. Wilson, 2001, Teratology.

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

C. Ferencz, I. Lurie, 1997, American journal of medical genetics.

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

I. Lurie, 2007, European journal of medical genetics.

Chromosome 7 abnormalities in parents of children with holoprosencephaly and hydronephrosis.

I. Lurie, H. Ilyina, L. Podleschuk, 1990, American journal of medical genetics.

De novo dup p/del q or dup q/del p Rearranged Chromosomes: Review of 104 Cases of a Distinct Chromosomal Mutation

H. Rivera, I. Lurie, M. G. Domínguez, 2013, Cytogenetic and Genome Research.

Interrupted aortic arch: an epidemiologic study.

C. Loffredo, C. Ferencz, P. Wilson, 2000, Teratology.

Phenotypic variability of del(2) (q22-q23): report of a case with a review of the literature.

I. Lurie, E. Wulfsberg, L. Rosenblum-Vos, 1994, Genetic counseling.

Non-cardiac malformations in individuals with outflow tract defects of the heart: the Baltimore-Washington Infant Study (1981-1989).

C. Loffredo, A. Kappetein, C. Ferencz, 1995, American journal of medical genetics.

Renal agenesis as a diagnostic feature of the crypthophthalmos‐syndactyly syndrome

I. Lurie, E. Cherstvoy, 1984, Clinical genetics.

Distal trisomy 14q.

R. Mikelsaar, I. Lurie, T. Ilus, 1987, Journal of medical genetics.

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

L. Livshits, P. Patsalis, C. Graziano, 2015, Cytogenetic and Genome Research.

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

I. Lurie, 2016, Taiwanese journal of obstetrics & gynecology.

Further delineation of the branchio-oculo-facial syndrome.

H. Brunner, R. Gorlin, A. Lin, 1995, American journal of medical genetics.

Phenotypic mapping and clinical ideology.

J. Opitz, I. Lurie, 1995, American journal of medical genetics.

The Wolf‐Hirschhorn syndrome

G. Lazjuk, I. Lurie, E. Cherstvoy, 1980 .

Wolf-Hirschhorn syndrome.

G. Lazjuk, I. Lurie, G. S. Coffin, 1971, American journal of diseases of children.

[Probability rates for different pregnancy outcomes in carriers of reciprocal chromosomal translocations involving chromosome 13].

I. Lurie, B. Panasiuk, A. Midro, 2008, Ginekologia polska.

Partial trisomy 10p in two generations

G. Lazjuk, I. Lurie, G. I. Kravtzova, 1978, Human Genetics.

[Probability rate of unbalanced offspring at birth and risk of unfavorable pregnancy outcomes in families of carriers of chromosomal reciprocal translocations involving chromosome 7].

K. Chrzanowska, Katarzyna Kozłowska, A. Gutkowska, 2013, Ginekologia polska.

The Neu‐Laxova syndrome—a distinct entity

G. Lazjuk, J. M. Optiz, I. Lurie, 1979 .

Unusual complex of congenital malformations.

I. Lurie, T. Zolotukhina, H. Ilyina, 1993, American journal of medical genetics.

Meckel syndrome in different populations.

I. Lurie, A. N. Prytkov, L. V. Meldere, 1984, American journal of medical genetics.

Atypical case of Aarskog syndrome.

R. Mikelsaar, I. Lurie, 1992, Journal of medical genetics.

Aprosencephaly-atelencephaly and the aprosencephaly (XK) syndrome

G. Lazjuk, J. M. Optiz, I. Lurie, 1979 .

Uniparental disomy 7 in Silver-Russell syndrome and primordial growth retardation.

K. Méhes, B. Hamel, B. Hamel, 1995, Human molecular genetics.

Complex chromosomal rearrangements: some breakpoints may have cellular adaptive significance

I. Lurie, E. Wulfsberg, M. Cohen, 1994, Clinical Genetics.

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

V. Fedotov, I. Lurie, H. Ilyina, 1995, American journal of medical genetics.

Reciprocal chromosome translocations involving short arm of chromosome 9 as a risk factor of unfavorable pregnancy outcomes after meiotic malsegregation 2:2.

J. Danik, B. Kałużewski, R. Leśniewicz, 2009, Advances in medical sciences.

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

J. Castrillo, S. Ávila, I. Lurie, 2015, American journal of medical genetics. Part A.

Kidney abnormalities in persons with monosomy 15q26

I. Lurie, 2008, American journal of medical genetics. Part A.

Maternal uniparental disomy 7 – review and further delineation of the phenotype

K. Chrzanowska, B. Hamel, A. Schinzel, 2000, European Journal of Pediatrics.

No evidence of uniparental disomy 2, 6, 14, 16, 20, and 22 as a major cause of intrauterine growth retardation

K. Méhes, A. Schinzel, D. Kotzot, 2000, Clinical genetics.

"Holoprosencephaly-polydactyly" (pseudotrisomy 13) syndrome: expansion of the phenotypic spectrum.

I. Lurie, E. Wulfsberg, I. W. Lurie, 1993, American journal of medical genetics.

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

I. Lurie, H. Ilyina, 1986, American journal of medical genetics. Supplement.

Phenotype of the Williams-Beuren syndrome associated with hemizygosity at the elastin locus

L. Brečević, W. Robinson, A. Schinzel, 1995, European Journal of Pediatrics.

Isochromosome 18p Results from Maternal Meiosis II Nondisjunction

L. Brečević, A. Schinzel, D. Kotzot, 1996, European journal of human genetics : EJHG.

Clinical Manifestations of Partial Trisomy 2p

I. Lurie, 2014, Cytogenetic and Genome Research.

Trisomy 2p: analysis of unusual phenotypic findings.

A. Schinzel, C. Castellan, I. Lurie, 1995, American journal of medical genetics.

The cerebro‐reno‐digital syndromes: a new community

G. Lazjuk, I. Lurie, E. Cherstvoy, 1991, Clinical genetics.

Distal trisomy 10q and limb defects.

I. Lurie, 2002, Annales de genetique.

Congenital anomalies of the ear, nose, and throat

I. Lurie, 1999 .

Difficulties in classification of the short rib-polydactyly syndromes

G. Lazjuk, I. Lurie, E. Cherstvoy, 2004, European Journal of Pediatrics.

Trisomy 17p11‐pter: unbalanced pericentric inversion, inv(17)(p11q25) in two patients, unbalanced translocations t(4;17)(q27;pl1) in a newborn and t(4;17)(pl6;p11.2) in a fetus

A. Schinzel, I. Lurie, F. Binkert, 1995, Clinical dysmorphology.

SYNDROME OF MULTIPLE CONGENITAL MALFORMATIONS INCLUDING PHOCOMELIA, THROMBOCYTOPENIA, ENCEPHALOCELE, AND UROGENITAL ABNORMALITIES

G. Lazjuk, I. Lurie, E. Cherstvoy, 1980, The Lancet.

"Pure" partial trisomy 4q25-qter owing to a de novo 4;22 translocation.

R. Mikelsaar, I. Lurie, T. Ilus, 1996, Journal of medical genetics.

von Voss-Cherstvoy syndrome: a variable perinatally lethal syndrome of multiple congenital anomalies.

H. Hoyme, S. Kahler, M. Lubinsky, 1994, American journal of medical genetics.

Where to look for the genes related to diaphragmatic hernia?

I. Lurie, I. W. Lurie, 2003, Genetic counseling.

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

I. Lurie, 1994, American journal of medical genetics.

The syndrome associated with the partial D-monosomy

I. Lurie, D. J. Orbeli, Ju. L. Goroshenko, 1971, Humangenetik.

Trisomy 8p due to the 3:1 segregation of the balanced translocation t(8;15)mat

G. Lazjuk, I. Lurie, M. Nedzved, 1979, Human Genetics.

Trisomy 4p and ocular defects.

I. Lurie, V. Samochvalov, 1994, The British journal of ophthalmology.

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

S. Schwartz, M. Cohen, M. Schwartz, 1995, American journal of medical genetics.

Genetics of the +p9 syndrome

G. Lazjuk, I. Lurie, D. B. Gurevich, 1976, Human Genetics.

Partial monosomies 18

G. Lazjuk, I. Lurie, 2004, Humangenetik.

Further studies on the genetic heterogeneity of cebocephaly.

G. Lazjuk, I. Lurie, M. Nedzved, 1976, Journal of medical genetics.

Dubowitz syndrome: possible evidence for a clinical subtype.

I. Lurie, H. Ilyina, 1990, American journal of medical genetics.

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

I. Lurie, 1995, American journal of medical genetics.

Down's syndrome with 45 chromosomes

I. Lurie, 2004, Human Genetics.

On the nosology of the "Schinzel-phocomelia" and "Al-Awadi/Raas-Rothschield" syndromes.

I. Lurie, E. Wulfsberg, 1993, American journal of medical genetics.

Partial trisomy 4q and preaxial limb defects

I. Lurie, 2005, American journal of medical genetics. Part A.

Trisomy for the distal part of the short arm of chromosome 3.

I. Lurie, D. V. Zaletajev, L. Smirnova, 1986, Helvetica paediatrica acta.

Atresia, stenosis and duplication of the gastro-intestinal tract: consideration of their origin.

I. Lurie, I. Kirillova, V. Kulazhenko, 1984, Acta morphologica Hungarica.

Spondylo-metaphyseal dysplasia: report of two cases of common type and delineation of a new variety with rectangular vertebral bodies

K. Kozłowski, I. Lurie, L. Brahimi, 1993, European Radiology.

The pathological anatomy of the Smith‐Lemli‐Opitz syndrome

G. Lazjuk, I. Lurie, E. Cherstvoy, 1975, Clinical genetics.

Letter to the editor: Familial omphalocele and recurrence risk

J. Opitz, I. Lurie, H. Ilyina, 1984 .

A syndrome of multiple congenital malformations including amelia and oligodactyly occurring in half‐cousins

G. Lazjuk, I. Lurie, E. Cherstvoy, 1976 .

Leptospirosis ictero-hemorrhagica (Weil's disease) treated with aureomycin; report of a case.

I. Lurie, 1949, Acta Medica Orientalia.

Pallister-Hall and McKusick-Kaufmann syndromes.

I. Lurie, 1995, Journal of medical genetics.

Neural tube defects in sibs of children with tracheo-oesophageal dysraphism.

I. Lurie, H. Ilyina, 1984, Journal of medical genetics.

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

I. Lurie, 1998, Clinical Genetics.

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

M. Cohen, I. Lurie, 1993, Clinical genetics.

Prenatal morphology of partial monosomy 18q.

G. Lazjuk, I. Lurie, T. Zolotukhina, 1987, Zentralblatt fur Gynakologie.

TREATMENT OF BARBITURATE POISONING

I. Lurie, 1954 .

Further evidence'for the autosomal‐recessive inheritance of the COFS syndrome

G. Lazjuk, I. Lurie, E. Cherstvoy, 1976, Clinical genetics.

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

C. Ferencz, I. Lurie, 1996, American journal of medical genetics.

Partial trisomy 5q and partial monosomy 5q within the same family

G. Lazjuk, I. Lurie, I. Shved, 1985, Clinical genetics.

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

J. Brenner, C. Ferencz, I. Lurie, 1996 .

11q;22q translocation: third case of imbalance not due to 3:1 nondisjunction in first meiosis.

I. Lurie, L. Podleschuk, 1992, American journal of medical genetics.

Trisomy 20p: case report and genetic review.

I. Lurie, N. Rumyantseva, D. V. Zaletajev, 1985, Journal de genetique humaine.

The smith-lemli-opitz syndrome

G. Lazjuk, I. Lurie, E. Cherstvoy, 1984, Virchows Archiv A.