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December 1973 (Volume 10, Number 4). [Index by author]

		Articles Articles Book Reviews Case Reports Research Article

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Articles

Myoglobin in Primary Muscular Disease: I. Duchenne Muscular Dystrophy: and: II. Muscular Dystrophy of Distal Type
A. E. Romero-Herrera, H. Lehmann, B. E. Tomlinson, and J. N. Walton
J Med Genet 1973; 10: 309-322. doi:10.1136/jmg.10.4.309 [Abstract] [PDF] [Request Permissions]

A `New' Saliva Substance, Probably Inherited, and Serologically Independent of ABH, Lewis, and Sd^a Blood Group Substances
P. Balding and E. R. Gold
J Med Genet 1973; 10: 323-327. doi:10.1136/jmg.10.4.323 [Abstract] [PDF] [Request Permissions]

Parental Dermatoglyphics in Down's Syndrome. A Ten-year Study
J. H. Priest, C. Verhulst, and S. Sirkin
J Med Genet 1973; 10: 328-332. doi:10.1136/jmg.10.4.328 [Abstract] [PDF] [Request Permissions]

The Relation of Sex of Affected Parent to the Age at Onset of Huntington's Disease
C. J. Brackenridge
J Med Genet 1973; 10: 333-336. doi:10.1136/jmg.10.4.333 [Abstract] [PDF] [Request Permissions]

Hirschsprung's Disease and Congenital Deafness
Rosalind Skinner and David Irvine
J Med Genet 1973; 10: 337-339. doi:10.1136/jmg.10.4.337 [Abstract] [PDF] [Request Permissions]

Genetic Association in Myocardial Infarction: Ethnicity; ABO, Rh, Le^a, Xg^a Blood Groups; G6PD Deficiency; and Abnormal Haemoglobins
N. Saha, C. C. S. Toh, and M. B. Ghosh
J Med Genet 1973; 10: 340-345. doi:10.1136/jmg.10.4.340 [Abstract] [PDF] [Request Permissions]

Lip Pits and Congenital Absence of Second Premolars: Varied Expression of the Lip Pits Syndrome
Edward L. Schneider
J Med Genet 1973; 10: 346-349. doi:10.1136/jmg.10.4.346 [Abstract] [PDF] [Request Permissions]

Fluorescence and Autoradiographic Studies in Patients with Turner's Syndrome and 46,XXp— and 46,XXq— Karyotypes
K. Boczkowski and Margareta Mikkelsen
J Med Genet 1973; 10: 350-355. doi:10.1136/jmg.10.4.350 [Abstract] [PDF] [Request Permissions]

D/D Translocations in Males Examined for Military Service
Eva Zeuthen and Johannes Nielsen
J Med Genet 1973; 10: 356-361. doi:10.1136/jmg.10.4.356 [Abstract] [PDF] [Request Permissions]

Segregation Analysis of A Large t(21q22q) Family
C. J. Chapman, R. J. M. Gardner, and A. M. O. Veale
J Med Genet 1973; 10: 362-366. doi:10.1136/jmg.10.4.362 [Abstract] [PDF] [Request Permissions]

Antenatal Diagnosis of Patau's Syndrome (Trisomy 13) including a Detailed Pathological Study of the Fetus
L. J. Butler, H. E. Reiss, N. E. France, and Sylvia Briddon
J Med Genet 1973; 10: 367-370. doi:10.1136/jmg.10.4.367 [Abstract] [PDF] [Request Permissions]

Sibship (21q21q) Translocation Down's Syndrome with Maternal Transmission
M. Furbetta, A. Falorni, P. Antignani, and A. Cao
J Med Genet 1973; 10: 371-375. doi:10.1136/jmg.10.4.371 [Abstract] [PDF] [Request Permissions]

Book Reviews

Oogenesis
Georgiana Jagiello
J Med Genet 1973; 10: 400. doi:10.1136/jmg.10.4.400 [PDF] [Request Permissions]

Genetic Factors in `Schizophrenia'
D. W. K. Kay
J Med Genet 1973; 10: 400-401. doi:10.1136/jmg.10.4.400-a [PDF] [Request Permissions]

Hermaphroditism, Genital Anomalies and Related Endocrine Disorders, 2nd ed
G. J. Dewhurst
J Med Genet 1973; 10: 401. doi:10.1136/jmg.10.4.401 [PDF] [Request Permissions]

Advances in Experimental Medicine and Biology
C. L. Berry
J Med Genet 1973; 10: 401. doi:10.1136/jmg.10.4.401-a [PDF] [Request Permissions]

Coefficients of Biological Distance
D. F. Roberts
J Med Genet 1973; 10: 401-402. doi:10.1136/jmg.10.4.401-b [PDF] [Request Permissions]

Human Embryology and Genetics
C. L. Berry
J Med Genet 1973; 10: 402. doi:10.1136/jmg.10.4.402 [PDF] [Request Permissions]

Genetic Studies in Mental Subnormality. Part 1: Familial Idiopathic Severe Subnormality: The Question of a Contribution by X-linked Genes
Renata Lax
J Med Genet 1973; 10: 402-403. doi:10.1136/jmg.10.4.402-a [PDF] [Request Permissions]

Basic Immunogenetics
R. Harris
J Med Genet 1973; 10: 403. doi:10.1136/jmg.10.4.403 [PDF] [Request Permissions]

Birth Defects: Original Article Series, 8
Anne H. Child
J Med Genet 1973; 10: 403-404. doi:10.1136/jmg.10.4.403-a [PDF] [Request Permissions]

Heritable Disorders in Orthopaedic Practice
T. J. Fairbank
J Med Genet 1973; 10: 404. doi:10.1136/jmg.10.4.404 [PDF] [Request Permissions]

Case Reports

A Child with Multiple Congenital Malformations and a 46,XX,t(Bq+;Dq–)/45,XX,–B, –D, + der(B),t(Bq+;Dq–) Karyotype
Alessandra Carnevale and Luis De Los Cobos
J Med Genet 1973; 10: 376-379. doi:10.1136/jmg.10.4.376 [Abstract] [PDF] [Request Permissions]

An Inherited Small Extra Chromosome: A Mother with 46,XX,t(17;22) (p1;q1) and a Son with 47,XY,+der(22) mat
Digamber S. Borgaonkar, Victor A. McKusick, and Phillip A. Farber
J Med Genet 1973; 10: 379-384. doi:10.1136/jmg.10.4.379 [Abstract] [PDF] [Request Permissions]

Segregating Reciprocal (4;21) (q21;q21) Translocation with Proposita Trisomic for Parts of 4q and 21
Albert De La Chapelle, Maila Koivisto, and Jim Schröder
J Med Genet 1973; 10: 384-389. doi:10.1136/jmg.10.4.384 [Abstract] [PDF] [Request Permissions]

Cryptophthalmos in Two Families from Bahia, Brazil
Eliane S. Azevêdo, Jesulino Biondi, and Luiz M. Ramalho
J Med Genet 1973; 10: 389-392. doi:10.1136/jmg.10.4.389 [Abstract] [PDF] [Request Permissions]

The Genetic Variability of Thalassaemia. A Family Study
E. De La Torre, E. Svarch, and B. Colombo
J Med Genet 1973; 10: 392-395. doi:10.1136/jmg.10.4.392 [Abstract] [PDF] [Request Permissions]

Research Article

Correspondence: Alport's syndrome.
O Mayo
J Med Genet 1973; 10: 396-398. doi:10.1136/jmg.10.4.396 [PDF] [Request Permissions]

Letter: The Crouzon syndrome.
K L Jones and M M Cohen, Jr
J Med Genet 1973; 10: 398-399. doi:10.1136/jmg.10.4.398 [PDF] [Request Permissions]

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	Myoglobin in Primary Muscular Disease: I. Duchenne Muscular Dystrophy: and: II. Muscular Dystrophy of Distal Type A. E. Romero-Herrera, H. Lehmann, B. E. Tomlinson, and J. N. Walton J Med Genet 1973; 10: 309-322. doi:10.1136/jmg.10.4.309 [Abstract] [PDF] [Request Permissions]

	A `New' Saliva Substance, Probably Inherited, and Serologically Independent of ABH, Lewis, and Sd^a Blood Group Substances P. Balding and E. R. Gold J Med Genet 1973; 10: 323-327. doi:10.1136/jmg.10.4.323 [Abstract] [PDF] [Request Permissions]

	Parental Dermatoglyphics in Down's Syndrome. A Ten-year Study J. H. Priest, C. Verhulst, and S. Sirkin J Med Genet 1973; 10: 328-332. doi:10.1136/jmg.10.4.328 [Abstract] [PDF] [Request Permissions]

	The Relation of Sex of Affected Parent to the Age at Onset of Huntington's Disease C. J. Brackenridge J Med Genet 1973; 10: 333-336. doi:10.1136/jmg.10.4.333 [Abstract] [PDF] [Request Permissions]

	Hirschsprung's Disease and Congenital Deafness Rosalind Skinner and David Irvine J Med Genet 1973; 10: 337-339. doi:10.1136/jmg.10.4.337 [Abstract] [PDF] [Request Permissions]

	Genetic Association in Myocardial Infarction: Ethnicity; ABO, Rh, Le^a, Xg^a Blood Groups; G6PD Deficiency; and Abnormal Haemoglobins N. Saha, C. C. S. Toh, and M. B. Ghosh J Med Genet 1973; 10: 340-345. doi:10.1136/jmg.10.4.340 [Abstract] [PDF] [Request Permissions]

	Lip Pits and Congenital Absence of Second Premolars: Varied Expression of the Lip Pits Syndrome Edward L. Schneider J Med Genet 1973; 10: 346-349. doi:10.1136/jmg.10.4.346 [Abstract] [PDF] [Request Permissions]

	Fluorescence and Autoradiographic Studies in Patients with Turner's Syndrome and 46,XXp— and 46,XXq— Karyotypes K. Boczkowski and Margareta Mikkelsen J Med Genet 1973; 10: 350-355. doi:10.1136/jmg.10.4.350 [Abstract] [PDF] [Request Permissions]

	D/D Translocations in Males Examined for Military Service Eva Zeuthen and Johannes Nielsen J Med Genet 1973; 10: 356-361. doi:10.1136/jmg.10.4.356 [Abstract] [PDF] [Request Permissions]

	Segregation Analysis of A Large t(21q22q) Family C. J. Chapman, R. J. M. Gardner, and A. M. O. Veale J Med Genet 1973; 10: 362-366. doi:10.1136/jmg.10.4.362 [Abstract] [PDF] [Request Permissions]

	Antenatal Diagnosis of Patau's Syndrome (Trisomy 13) including a Detailed Pathological Study of the Fetus L. J. Butler, H. E. Reiss, N. E. France, and Sylvia Briddon J Med Genet 1973; 10: 367-370. doi:10.1136/jmg.10.4.367 [Abstract] [PDF] [Request Permissions]

	Sibship (21q21q) Translocation Down's Syndrome with Maternal Transmission M. Furbetta, A. Falorni, P. Antignani, and A. Cao J Med Genet 1973; 10: 371-375. doi:10.1136/jmg.10.4.371 [Abstract] [PDF] [Request Permissions]

	Oogenesis Georgiana Jagiello J Med Genet 1973; 10: 400. doi:10.1136/jmg.10.4.400 [PDF] [Request Permissions]

	Genetic Factors in `Schizophrenia' D. W. K. Kay J Med Genet 1973; 10: 400-401. doi:10.1136/jmg.10.4.400-a [PDF] [Request Permissions]

	Hermaphroditism, Genital Anomalies and Related Endocrine Disorders, 2nd ed G. J. Dewhurst J Med Genet 1973; 10: 401. doi:10.1136/jmg.10.4.401 [PDF] [Request Permissions]

	Advances in Experimental Medicine and Biology C. L. Berry J Med Genet 1973; 10: 401. doi:10.1136/jmg.10.4.401-a [PDF] [Request Permissions]

	Coefficients of Biological Distance D. F. Roberts J Med Genet 1973; 10: 401-402. doi:10.1136/jmg.10.4.401-b [PDF] [Request Permissions]

	Human Embryology and Genetics C. L. Berry J Med Genet 1973; 10: 402. doi:10.1136/jmg.10.4.402 [PDF] [Request Permissions]

	Genetic Studies in Mental Subnormality. Part 1: Familial Idiopathic Severe Subnormality: The Question of a Contribution by X-linked Genes Renata Lax J Med Genet 1973; 10: 402-403. doi:10.1136/jmg.10.4.402-a [PDF] [Request Permissions]

	Basic Immunogenetics R. Harris J Med Genet 1973; 10: 403. doi:10.1136/jmg.10.4.403 [PDF] [Request Permissions]

	Birth Defects: Original Article Series, 8 Anne H. Child J Med Genet 1973; 10: 403-404. doi:10.1136/jmg.10.4.403-a [PDF] [Request Permissions]

	Heritable Disorders in Orthopaedic Practice T. J. Fairbank J Med Genet 1973; 10: 404. doi:10.1136/jmg.10.4.404 [PDF] [Request Permissions]

	A Child with Multiple Congenital Malformations and a 46,XX,t(Bq+;Dq–)/45,XX,–B, –D, + der(B),t(Bq+;Dq–) Karyotype Alessandra Carnevale and Luis De Los Cobos J Med Genet 1973; 10: 376-379. doi:10.1136/jmg.10.4.376 [Abstract] [PDF] [Request Permissions]

	An Inherited Small Extra Chromosome: A Mother with 46,XX,t(17;22) (p1;q1) and a Son with 47,XY,+der(22) mat Digamber S. Borgaonkar, Victor A. McKusick, and Phillip A. Farber J Med Genet 1973; 10: 379-384. doi:10.1136/jmg.10.4.379 [Abstract] [PDF] [Request Permissions]

	Segregating Reciprocal (4;21) (q21;q21) Translocation with Proposita Trisomic for Parts of 4q and 21 Albert De La Chapelle, Maila Koivisto, and Jim Schröder J Med Genet 1973; 10: 384-389. doi:10.1136/jmg.10.4.384 [Abstract] [PDF] [Request Permissions]

	Cryptophthalmos in Two Families from Bahia, Brazil Eliane S. Azevêdo, Jesulino Biondi, and Luiz M. Ramalho J Med Genet 1973; 10: 389-392. doi:10.1136/jmg.10.4.389 [Abstract] [PDF] [Request Permissions]

	The Genetic Variability of Thalassaemia. A Family Study E. De La Torre, E. Svarch, and B. Colombo J Med Genet 1973; 10: 392-395. doi:10.1136/jmg.10.4.392 [Abstract] [PDF] [Request Permissions]

	Correspondence: Alport's syndrome. O Mayo J Med Genet 1973; 10: 396-398. doi:10.1136/jmg.10.4.396 [PDF] [Request Permissions]

	Letter: The Crouzon syndrome. K L Jones and M M Cohen, Jr J Med Genet 1973; 10: 398-399. doi:10.1136/jmg.10.4.398 [PDF] [Request Permissions]