B. Weisskopf

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Behavioral Correlates in the Happy Puppet Syndrome: a Characteristic Profile?

A. Zimmerman, R. Greenstein, J. Hersh, 1981, Developmental medicine and child neurology.

Sternal malformation/vascular dysplasia association.

J. Opitz, J. Rutledge, M. Harrod, 1985, American journal of medical genetics.

Clinical correlations in partial hypoxanthine guanine phosphoribosyltransferase deficiency.

W. Nyhan, J. Seegmiller, T. Page, 1986, Pediatric neurology.

Methylphenidate-induced delusional disorder in a child with attention deficit disorder with hyperactivity.

A. Bloom, B. Weisskopf, L. J. Russell, 1988, Journal of the American Academy of Child and Adolescent Psychiatry.

Hypoglycemia in the newborn.

M. Cornblath, B. Weisskopf, K. R. Swiatek, 1966, Pediatric clinics of North America.

Chromosome aberrations in the child of a kidney transplant recipient.

B. Weisskopf, D. E. Leb, B. S. Kanovitz, 1971, Archives of internal medicine.

Townes Syndrome

R. Solinger, J. Hersh, B. Weisskopf, 1986, Clinical pediatrics.

Ivemark's "asplenia" syndrome: a single gene disorder.

J. Hersh, B. Weisskopf, L. J. Russell, 1989, Southern medical journal.

Pseudo-Menke syndrome.

N. Dinno, B. Weisskopf, U. Yacoub, 1981, The Journal of pediatrics.

Trisomy for the short arms of chromosome 9 in two generations, with balanced translocations t(15p+;9q−) in three generations

B. Weisskopf, P. E. Podruch, 1974 .

47, XY, t(9p+;11q+) in a male infant with multiple malformations

N. Dinno, B. Weisskopf, G. Silvey, 1974 .

Retinoic acid embryopathy: timing of exposure and effects on fetal development.

J. Hersh, B. Weisskopf, M. E. Hand, 1985, JAMA.

Vaginal uterine agenesis associated with amastia in a phenotypic female with a de novo 46,XX,t(8;13)(q22.1;q32.1) translocation.

B. Weisskopf, F. Yen, L. Amesse, 1999, Clinical genetics.

Median cleft face syndrome.

B. Weisskopf, W. C. Edwards, W. Askew, 1971, American journal of ophthalmology.

Trisomy for the short arms of chromosome 9 in two generations, with balanced translocations t(15pplus;9qminus) in three generations.

B. Weisskopf, P. E. Podruch, 1974, The Journal of pediatrics.

47, XY, t(9pplus;11qplus) in a mlae infant with multiple malformations.

N. Dinno, B. Weisskopf, G. Silvey, 1974, Clinical genetics.

Cognition in cerebral gigantism: are the estimates of mental retardation too high?

J. Hersh, A. Bloom, N. Dinno, 1983, Journal of developmental and behavioral pediatrics : JDBP.

Psychological Aspects of Cerebral Gigantism

B. Patterson, A. Bloom, B. Weisskopf, 1978 .

A terminal deletion (14)(q31.1) in a child with microcephaly, narrow palate, gingival hypertrophy, protuberant ears, and mild mental retardation.

F. Yen, B. Weisskopf, P. E. Podruch, 1989, Journal of medical genetics.

Yq- in a child with livedo reticularis, snub nose, microcephaly, and profound mental retardation.

F. Yen, N. Dinno, B. Weisskopf, 1982, Journal of medical genetics.

Forearm fullness in Coffin-Lowry syndrome: a misleading yet possible early diagnostic clue.

J. Opitz, C. Decoster, J. Hersh, 1984, American journal of medical genetics.

Childhood Autism in a female with Coffin Siris Syndrome.

J. Hersh, A. Bloom, B. Weisskopf, 1982, Journal of Developmental and Behavioral Pediatrics.

Mild intellectual deficits in a child with 49,XXXXY.

C. Topinka, F. Yen, J. Hersh, 1988, Research in developmental disabilities.

Syndrome of Growth Resistance, Obesity, and Intellectual Impairment with Precocious Puberty

B. Weisskopf, D. Macmillan, Chong Bin Kim, 1972, Archives of disease in childhood.

Does a supernumerary nipple/renal field defect exist?

J. Hersh, A. Bloom, B. Weisskopf, 1987, American journal of diseases of children.