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Familial XY gonadal dysgenesis

The New England journal of medicine, 1968-03, Vol.278 (13), p.695-700

1968

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AN INVESTIGATION OF 171 POSSIBLE LINKAGE RELATIONSHIPS IN MAN

Annals of eugenics, 1946-01, Vol.13 (1), p.35-71

KLOEPFER, H. W.

1946

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Genetic penetrance from MZ twins of absent C-triradius, a palmar dermatoglyphic trait

Acta geneticae medicae et gemellologiae, 1976, Vol.25 (1), p.177-180

1976

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Genetic determination of acute disseminated histiocytosis X

Pediatrics (Evanston), 1970-05, Vol.45 (5), p.753-765

1970

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Familial anorectal anomalies

Pediatrics (Evanston), 1961-02, Vol.27 (2), p.334-336

1961

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Parameters used to describe less common single major genes expressed in dermatoglyphic features

Progress in clinical and biological research, 1982, Vol.84, p.105

Kloepfer, H W

1982

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Genetic Aspects of Congenital Hearing Loss

American annals of the deaf (Washington, D.C. 1886), 1970-01, Vol.115 (1), p.17-22

1970

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Possible genetic carriers in the spherophakia-brachymorphia syndrome

American journal of human genetics, 1955-12, Vol.7 (4), p.398-425

1955

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Homozygous expression of a dominant gene for charcot-marie-tooth neuropathy

Annals of neurology, 1979-06, Vol.5 (6), p.515-522

1979

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The spherophakia-brachymorphia syndrome

A.M.A. archives of ophthalmology, 1956-01, Vol.55 (1), p.28-35

1956

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The hereditary snydrome of congenital deafness and retinitis pigmentosa

The Laryngoscope, 1996, Vol.76 (5), p.850-862

1996

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The detection of the genotype for absent c-triradius in individuals with main line sequence CBD

Birth defects original article series, 1979, Vol.15 (6), p.511

Kloepfer, H W

1979

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Penetrance of gene for absent c-triradius from 567 sets of monozygotic twins

Progress in clinical and biological research, 1978, Vol.24 Pt C, p.269

1978

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The inheritance of the hypothenar whorl

Birth defects original article series, 1979, Vol.15 (6), p.543

1979

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The immunochemistry and genetics of blood group O. II. A study of the secretion of blood group A, B and O (H) substances in the saliva of family groups using precipitating antibody prepared in chickens

The Journal of immunology (1950), 1961-09, Vol.87, p.342

1961

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Genetics of microcephaly in Louisiana

Proceedings of the annual meeting of the American Psychopathological Association, 1967, Vol.56, p.244

1967

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Hereditary blepharophimosis, ptosis, and epicanthus inversus

The Journal of the International College of Surgeons, 1960-05, Vol.33, p.558

1960

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MANIFESTATIONS OF A RECESSIVE GENE FOR MICROCEPHALY IN A POPULATION ISOLATE

Journal de genetique humaine, 1964, Vol.13, p.52

1964

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AUTOSOMAL RECESSIVE INHERITANCE OF DUCHENNE‐TYPE MUSCULAR DYSTROPHY

Annals of human genetics, 1957-11, Vol.22 (2), p.138-143

1957

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The detection of carriers in hereditary myoclonic epilepsy

Acta geneticae medicae et gemellologiae, 1960-10, Vol.9 (4), p.466-471

1960

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Homozygous Expression of a Dominant Gene Causing Peroneal Muscular Atrophy (Charcot-Marie-Tooth Disease)

Acta geneticae medicae et gemellologiae, 1974-01, Vol.23 (S1), p.217-220

1974

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An acromegaloid, cutis verticis gyrata, corneal leukoma syndrome. A new medical entity

Archives of ophthalmology (1960), 1962-12, Vol.68 (6), p.722

1962

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Autosomal recessive inheritance of Duchennetype muscular dystrophy

Annals of human genetics, 1958-02, Vol.22 (2), p.138-143

1958

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AUTOSOMAL RECESSIVE INHERITANCE OF DUCHENNE-TYPE MUSCULAR DYSTROPHY

Human heredity, 1957, Vol.7 (2), p.314-318

1957

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The hereditary syndrome of congenital deafness and retinitis pigmentosa. (Usher's syndrome)

The Laryngoscope, 1966-05, Vol.76 (5), p.850-862

1966

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Familial XY gonadal dysgenesis

AN INVESTIGATION OF 171 POSSIBLE LINKAGE RELATIONSHIPS IN MAN

Genetic penetrance from MZ twins of absent C-triradius, a palmar dermatoglyphic trait

Genetic determination of acute disseminated histiocytosis X

Familial anorectal anomalies

Parameters used to describe less common single major genes expressed in dermatoglyphic features

Genetic Aspects of Congenital Hearing Loss

Possible genetic carriers in the spherophakia-brachymorphia syndrome

Homozygous expression of a dominant gene for charcot-marie-tooth neuropathy

The spherophakia-brachymorphia syndrome

The hereditary snydrome of congenital deafness and retinitis pigmentosa

The detection of the genotype for absent c-triradius in individuals with main line sequence CBD

Penetrance of gene for absent c-triradius from 567 sets of monozygotic twins

The inheritance of the hypothenar whorl

The immunochemistry and genetics of blood group O. II. A study of the secretion of blood group A, B and O (H) substances in the saliva of family groups using precipitating antibody prepared in chickens

Genetics of microcephaly in Louisiana

Hereditary blepharophimosis, ptosis, and epicanthus inversus

MANIFESTATIONS OF A RECESSIVE GENE FOR MICROCEPHALY IN A POPULATION ISOLATE

AUTOSOMAL RECESSIVE INHERITANCE OF DUCHENNE‐TYPE MUSCULAR DYSTROPHY

The detection of carriers in hereditary myoclonic epilepsy

Homozygous Expression of a Dominant Gene Causing Peroneal Muscular Atrophy (Charcot-Marie-Tooth Disease)

An acromegaloid, cutis verticis gyrata, corneal leukoma syndrome. A new medical entity

Autosomal recessive inheritance of Duchennetype muscular dystrophy

AUTOSOMAL RECESSIVE INHERITANCE OF DUCHENNE-TYPE MUSCULAR DYSTROPHY

The hereditary syndrome of congenital deafness and retinitis pigmentosa. (Usher's syndrome)

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