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South African Medical Journal = Suid-Afrikaanse Tydskrif Vir Geneeskunde
|
August 24, 1974
Medical genetics in clinical practice
P H Beighton, M M Nelson
Archives of Otolaryngology (Chicago, Ill. : 1960)
|
April 1, 1978
Deafness in Osteodysplasty of Melnick and Needles
S L Sellars, P H Beighton
Journal of Medical Genetics
|
May 1, 1989
Synchrony of oculocutaneous albinism, the Prader-Willi syndrome, and a normal karyotype
C E Wallis, P H Beighton
Clinical Genetics
|
February 1, 1978
Osteopathia striata with cranial sclerosis. An autosomal dominant entity
F T Horan, P H Beighton
South African Medical Journal = Suid-Afrikaanse Tydskrif Vir Geneeskunde
|
August 3, 1974
Cytogenetics in medical practice
M M Nelson, P H Beighton
The Journal of Bone and Joint Surgery. British Volume
|
February 1, 1978
"Osteopetrosis" in the Fairbank Collection
F T Horan, P H Beighton
The Journal of Bone and Joint Surgery. British Volume
|
May 1, 1980
Infantile metaphysial dysplasia or "battered babies"? A reassessment of material in the Fairbank Collection
F T Horan, P H Beighton
Birth Defects Original Article Series
|
February 1, 1971
Roussy-Levy hereditary areflexic dystasis presenting as Charcot-Marie-Tooth syndrome
J L Murdoch, P H Beighton
The Journal of Clinical Pediatric Dentistry
|
November 5, 2002
Oro-dental manifestations of the Schwartz-Jampel syndrome
L X G Stephen, P H Beighton
South African Medical Journal = Suid-Afrikaanse Tydskrif Vir Geneeskunde
|
February 16, 1991
Duchenne muscular dystrophy--a molecular service
R Ballo, H W Hitzeroth, P H Beighton
Page
of 4
Search research articles
Search
Showing results (11-20 of 38) with videos related to
Sort By:
Page
of 4
South African Medical Journal = Suid-Afrikaanse Tydskrif Vir Geneeskunde
|
August 24, 1974
Medical genetics in clinical practice
P H Beighton, M M Nelson
Archives of Otolaryngology (Chicago, Ill. : 1960)
|
April 1, 1978
Deafness in Osteodysplasty of Melnick and Needles
S L Sellars, P H Beighton
Journal of Medical Genetics
|
May 1, 1989
Synchrony of oculocutaneous albinism, the Prader-Willi syndrome, and a normal karyotype
C E Wallis, P H Beighton
Clinical Genetics
|
February 1, 1978
Osteopathia striata with cranial sclerosis. An autosomal dominant entity
F T Horan, P H Beighton
South African Medical Journal = Suid-Afrikaanse Tydskrif Vir Geneeskunde
|
August 3, 1974
Cytogenetics in medical practice
M M Nelson, P H Beighton
The Journal of Bone and Joint Surgery. British Volume
|
February 1, 1978
"Osteopetrosis" in the Fairbank Collection
F T Horan, P H Beighton
The Journal of Bone and Joint Surgery. British Volume
|
May 1, 1980
Infantile metaphysial dysplasia or "battered babies"? A reassessment of material in the Fairbank Collection
F T Horan, P H Beighton
Birth Defects Original Article Series
|
February 1, 1971
Roussy-Levy hereditary areflexic dystasis presenting as Charcot-Marie-Tooth syndrome
J L Murdoch, P H Beighton
The Journal of Clinical Pediatric Dentistry
|
November 5, 2002
Oro-dental manifestations of the Schwartz-Jampel syndrome
L X G Stephen, P H Beighton
South African Medical Journal = Suid-Afrikaanse Tydskrif Vir Geneeskunde
|
February 16, 1991
Duchenne muscular dystrophy--a molecular service
R Ballo, H W Hitzeroth, P H Beighton
Page
of 4