M. Harrod

发表

Familial incomplete male pseudohermaphroditism, type 2. Decreased dihydrotestosterone formation in pseudovaginal perineoscrotal hypospadias.

J. D. Wilson, P. Walsh, J. Goldstein, 1974, The New England journal of medicine.

Sternal malformation/vascular dysplasia association.

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

Verification of the fetal valproate syndrome phenotype.

S. Clarren, J. Atkin, L. Elsas, 1988, American journal of medical genetics.

Homozygous familial hypercholesterolemia: specificity of the biochemical defect in cultured cells and feasibility of prenatal detection.

M. Brown, J. Goldstein, Michael S. Brown, 1974, American journal of human genetics.

Familial incomplete male pseudohermaphroditism, type 1. Evidence for androgen resistance and variable clinical manifestations in a family with the Reifenstein syndrome.

J. D. Wilson, J. Goldstein, P. Macdonald, 1974, The New England journal of medicine.

del(20p) with manifestations of arteriohepatic dysplasia.

J. Friedman, J. Byrne, M. Harrod, 1986, American journal of medical genetics.

Risk of chromosomal abnormalities, with emphasis on live-born offspring of young mothers.

B. B. Little, S. Ramin, N. Schneider, 1995, American journal of human genetics.

A "new" lethal multiple congenital anomaly syndrome: joint contractures, cerebellar hypoplasia, renal hypoplasia, urogenital anomalies, tongue cysts, shortness of limbs, eye abnormalities, defects of the heart, gallbladder agenesis, and ear malformations.

J. Friedman, J. Rutledge, H. Chen, 1984, American journal of medical genetics.

Further delineation of Weaver syndrome.

R. Shprintzen, H. Hoyme, J. Welch, 1986, The Journal of pediatrics.

Developmental studies in Drosophila. VI. Ultrastructural analysis of the salivary glands of Drosophila pseudoobscura during the late larval period.

C. Kastritsis, M. Harrod, 1972, Journal of ultrastructure research.

Developmental studies in Drosophila. II. Ultrastructural analysis of the salivary glands of Drosophila pseudoobscura during some stages of development.

C. Kastritsis, M. Harrod, 1972, Journal of ultrastructure research.

Familial absorptive hypercalciuria in a large kindred.

C. Pak, R. Peterson, M. Harrod, 1981, The Journal of urology.

Congenital absence of the vagina. The Mayer-Rokitansky-Kuster-Hauser syndrome.

J. Griffin, J. Madden, C. Edwards, 1976, Annals of internal medicine.

Methotrexate and reproduction in men: case report and recommendations.

M. Menter, L. Morris, M. Harrod, 1993, Journal of the American Academy of Dermatology.

Duplication 12q mosaicism in two unrelated patients with a similar syndrome.

U. Francke, J. M. Optiz, M. Harrod, 1980, American journal of medical genetics.

Complementary duplication and deletion of 17 (pcen----p11.2): a family with a supernumerary chromosome comprised of an interstitially deleted segment.

J. Friedman, M. Harrod, P. Howard‐Peebles, 1992, American journal of medical genetics.

Fryns syndrome: prenatal diagnosis and pathologic correlation.

C. Timmons, D. Twickler, J. Sheffield, 1998, Journal of ultrasound in medicine : official journal of the American Institute of Ultrasound in Medicine.

An unusual connective tissue disease in mother and son: A “new” type of Ehlers‐Danlos syndrome?

M. Harrod, J. Friedman, 1982, Clinical genetics.

Polycystic kidney disease in a patient with the oral‐facial‐digital syndrome‐Type I *

J. Stokes, M. Harrod, J. Goldstein, 1976, Clinical genetics.

α‐L‐iduronidase deficiency and possible Hurler‐Scheie genetic compound

R. Rosenberg, J. Kirkpatrick, M. Harrod, 1976, Neurology.

A cutaneous marker in the Hunter syndrome a report of four cases.

J. Herndon, I. Maumenee, R. Freeman, 1977, Archives of dermatology.

alpha-L-iduronidase deficiency and possible Hurler-Scheie genetic compound. Clinical, pathologic, and biochemical findings.

R. Rosenberg, J. Kirkpatrick, M. Harrod, 1976, Neurology.

Ring 17 chromosome detected by amniocentesis

A. Weinberg, M. Harrod, Janice L. Bair, 1975, Humangenetik.

Etiologic heterogeneity of fetal hydrocephalus diagnosed by ultrasound.

J. Friedman, A. Weinberg, J. Rutledge, 1984, American journal of obstetrics and gynecology.

Familial pseudomembranous colitis and its relation to lincomycin therapy

J. Goldstein, Michael S. Brown, A. Weinberg, 1975, The American Journal of Digestive Diseases.

Anatomic correlates of ultrasonographic prenatal diagnosis

A. Weinberg, J. Rutledge, M. Harrod, 1986, Prenatal Diagnosis.

Warfarin embryopathy in siblings.

M. Harrod, P. S. Sherrod, 1981, Obstetrics and gynecology.

EFFECTS OF VALPROIC ACID ON THE FETUS

A. Schinzel, J. Diliberti, J. Hanson, 1984, Pediatric Research.

INCIDENCE OF MAJOR CONGENITAL MALFORMATIONS IN OFFSPRING OF ALCOHOLICS AND POLYDRUG ABUSERS

A. Schinzel, J. Diliberti, H. Ardinger, 1984, Pediatric Research.