P. Kaplan

P. Byers, K. Nathanson, P. Kaplan, 1999, Pediatric and developmental pathology : the official journal of the Society for Pediatric Pathology and the Paediatric Pathology Society.

Autosomal dominant inheritance of small kidneys.

P. Kaplan, S. Jéquier, B. Kaplan, 1989, American journal of medical genetics.

Glutaric aciduria type II: review of the phenotype and report of an unusual glomerulopathy.

Golder N Wilson, P. Kaplan, F. Frerman, 1989, American journal of medical genetics.

Dyssegmental dysplasias: clinical, radiographic, and morphologic evidence of heterogeneity.

D. Rimoin, P. Kaplan, C. Clericuzio, 1987, American journal of medical genetics.

Piebaldism-Waardenburg syndrome: histopathologic evidence for a neural crest syndrome.

P. Kaplan, J. P. de Chaderévian, 1988, American journal of medical genetics.

A taxonomic approach to the del(4p) phenotype.

S. Aymé, P. Kaplan, M. Vekemans, 1985, American journal of medical genetics.

Molecular definition of the chromosome 7 deletion in Williams syndrome and parent-of-origin effects on growth.

U. Francke, B. Hamel, P. Kaplan, 1996, American journal of human genetics.

Renal anomalies and oligohydramnios in the cerebro-oculofacio-skeletal syndrome.

P. Kaplan, M. Preus, T. Kirkham, 1977, American journal of diseases of children.

Genes for the CPE receptor (CPETR1) and the human homolog of RVP1 (CPETR2) are localized within the Williams-Beuren syndrome deletion.

P. Kaplan, U. Francke, P. Kaplan, 1998, Genomics.

Kabuki syndrome is not caused by a microdeletion in the DiGeorge/velocardiofacial chromosomal region within 22q 11.2.

E. Zackai, N. Niikawa, D. Driscoll, 1996, American journal of medical genetics.

MCA/MR syndrome in a female infant with tetraploidy mosaicism: review of the human polyploid phenotype.

P. Kaplan, M. Vekemans, G. Wilson, 1988, American journal of medical genetics.

Lateral meningocele syndrome: three new patients and review of the literature.

E. Zackai, A. Duhaime, S. Zderic, 1997, American journal of medical genetics.

Further evidence that the Hajdu-Cheney syndrome and the "serpentine fibula-polycystic kidney syndrome" are a single entity.

E. Zackai, P. Kaplan, F. Ramos, 1998, American journal of medical genetics.

X linked recessive inheritance of agenesis of the corpus callosum.

P. Kaplan, 1983, Journal of medical genetics.

Ambiguous genitalia associated with skeletal abnormalities, cutis laxa, craniostenosis, psychomotor retardation, and facial abnormalities (SCARF syndrome).

A. Hunter, P. Kaplan, A. Hunter, 1989, American journal of medical genetics.

Skeletal and cardiac malformations with thrombocytopenia: a new syndrome?

A. Elliott, P. Kaplan, V. D. Der Kaloustian, 1996, American journal of medical genetics.

A "community" of face-limb malformation syndromes.

P. Kaplan, F. Fraser, C. Cummings, 1976, The Journal of pediatrics.

Diagnosis of chromosome 3 duplication q23----qter, deletion p25----pter in a patient with the C (trigonocephaly) syndrome.

P. Kaplan, M. Vekemans, M. Preus, 1986, American journal of medical genetics.

Increased renal medullary echogenicity in patients with Williams syndrome

P. Kaplan, S. Jéquier, G. Côté, 2006, Pediatric Radiology.

Variable expression of autosomal recessive polycystic kidney disease and congenital hepatic fibrosis within a family.

P. Kaplan, P. Russo, S. O'regan, 1988, American journal of medical genetics.

A spinal arteriovenous malformation with hereditary cutaneous hemangiomas.

P. Kaplan, R. Hollenberg, F. Fraser, 1976, American journal of diseases of children.

Kenny syndrome: description of additional abnormalities and molecular studies

P. Kaplan, G. Hendy, I. Bergadá, 1988, Human Genetics.

Pregnancy in a woman with the Brachmann-de Lange syndrome.

P. Kaplan, B. Buehler, W. Sanger, 1985, American journal of medical genetics.

Aniridia/glaucoma and Wilms tumor in a sibship with renal tubular acidosis and sensory nerve deafness.

P. Kaplan, M. Vekemans, B. Kaplan, 1987, American journal of medical genetics. Supplement.

Infantile spasms is associated with deletion of the MAGI2 gene on chromosome 7q11.23-q21.11.

Christian R Marshall, Alexandre Reymond, Paige Kaplan, 2008, American journal of human genetics.

Malformations and minor anomalies in children whose mothers had prenatal diagnosis: comparison between CVS and amniocentesis.

Golder N Wilson, P. Kaplan, M. Vekemans, 1990, American journal of medical genetics.

Distal deletion of chromosome 1q in an adult.

P. Kaplan, M. Vekemans, S. Zeesman, 1990, American journal of medical genetics.

Renal dysgenesis in a monozygotic twin: association with in utero exposure to indomethacin.

P. Kaplan, B. Kaplan, H. Rosenberg, 1991, American journal of medical genetics.

A new acro-cranio-facial dysostosis syndrome in sisters.

P. Kaplan, S. Jéquier, H. Plauchu, 1988, American journal of medical genetics.

Spectrum of elastin sequence variants and cardiovascular phenotypes in 49 patients with Williams–Beuren syndrome

C. Haldeman-Englert, T. Shaikh, B. Morrow, 2013, American Journal of Medical Genetics. Part A.

Inherited and congenital malformations of the kidneys in the neonatal period.

P. Kaplan, E. Ruchelli, B. Kaplan, 1992, Clinics in perinatology.

Prenatal Presentation of Congenital Chloride Diarrhea: Clinical Report and Review of the Literature

P. Kaplan, A. Kousoulis, N. Rose, 1992, American journal of perinatology.

Lethal osteogenesis imperfecta with amniotic band lesions: collagen studies.

P. Kaplan, J. Opitz, F. Glorieux, 1986, American journal of medical genetics.

A shortened beta-hexosaminidase alpha-chain in an Italian patient with infantile Tay-Sachs disease.

J. Bayleran, P. Kaplan, E. Neufeld, 1987, American journal of human genetics.