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Clinical Manifestations of Partial Trisomy 2p

Cytogenetic and genome research, 2014-01, Vol.144 (1), p.28-30

Lurie, Iosif W.

2014

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

Clinical dysmorphology, 2016-07, Vol.25 (3), p.133

Lurie, Iosif W

2016

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Partial trisomy 4q and preaxial limb defects

American journal of medical genetics. Part A, 2005-10, Vol.138A (3), p.304-305

Lurie, Iosif W.

2005

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

European journal of human genetics : EJHG, 2009-08, Vol.17 (8), p.1086-1091

2009

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

American journal of medical genetics. Part A, 2015-08, Vol.167A (8), p.1865-1871

2015

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Kidney abnormalities in persons with monosomy 15q26

American journal of medical genetics. Part A, 2008-07, Vol.146A (13), p.1761-1764

Lurie, Iosif W.

2008

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

Cytogenetic and genome research, 2014-01, Vol.144 (3), p.169-177

2014

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

European journal of medical genetics, 2007-07, Vol.50 (4), p.322-325

Lurie, Iosif W

2007

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

European journal of human genetics : EJHG, 2009-02, Vol.17 (8), p.1086-1091

2009

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

Ginekologia polska, 2013-12, Vol.84 (12), p.992-1004

2013

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

Human molecular genetics, 1995-04, Vol.4 (4), p.583-587

1995

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

Ginekologia polska, 2008-07, Vol.79 (7), p.477-482

2008

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Genetics of the Costello syndrome

American journal of medical genetics, 1994-09, Vol.52 (3), p.358-359

Lurie, Iosif W.

1994

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

Clinical genetics, 1998-07, Vol.54 (1), p.108-109

Lurie, Iosif W.

1998

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Ectrodactyly and tetralogy of Fallot in a fetus with del(6)(q21q23)

Genetic counseling, 2014, Vol.25 (1), p.19

2014

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Trisomy 2p: Analysis of unusual phenotypic findings

American journal of medical genetics, 1995-01, Vol.55 (2), p.229-236

1995

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Distal trisomy 10q and limb defects

Annales de génétique, 2002-07, Vol.45 (3), p.127-129

Lurie, Iosif W.

2002

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

Teratology (Philadelphia), 2001-02, Vol.63 (2), p.87-93

2001

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Isochromosome 18p results from maternal meiosis II nondisjunction

European journal of human genetics : EJHG, 1996, Vol.4 (3), p.168-174

1996

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

American journal of medical genetics, 1997-05, Vol.70 (2), p.144-149

1997

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Letter to the editor: Familial omphalocele and recurrence risk

American journal of medical genetics, 1984-02, Vol.17 (2), p.541-543

1984

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Aprosencephaly-atelencephaly and the aprosencephaly (XK) syndrome

American journal of medical genetics, 1979, Vol.3 (3), p.303-309

1979

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Trisomy 4p and ocular defects

British journal of ophthalmology, 1994-05, Vol.78 (5), p.415-417

1994

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

American journal of medical genetics, 1995-04, Vol.56 (3), p.308-311

Lurie, Iosif W.

1995

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Complex chromosomal rearrangements: some breakpoints may have cellular adaptive significance

Clinical genetics, 1994-09, Vol.46 (3), p.244-247

1994

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Clinical Manifestations of Partial Trisomy 2p

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

Partial trisomy 4q and preaxial limb defects

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

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

Kidney abnormalities in persons with monosomy 15q26

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

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

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

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

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

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

Genetics of the Costello syndrome

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

Ectrodactyly and tetralogy of Fallot in a fetus with del(6)(q21q23)

Trisomy 2p: Analysis of unusual phenotypic findings

Distal trisomy 10q and limb defects

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

Isochromosome 18p results from maternal meiosis II nondisjunction

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

Letter to the editor: Familial omphalocele and recurrence risk

Aprosencephaly-atelencephaly and the aprosencephaly (XK) syndrome

Trisomy 4p and ocular defects

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

Complex chromosomal rearrangements: some breakpoints may have cellular adaptive significance

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