Cytogenetics

226. ALFI, O., DERENCSENYI, A., DONNELL, G. (1975) ‘Chromosome polymorphism and prenatal diagnosis.’ Lancet, i, 1253. (Letter.) 227. ALLER, V., ABRISQUETA, J. A., PEREZ, A., MARTIN, M. A., GODAY, C., DEL MAZO, J. (1975) ‘A case of trisomy 8 mosaicism 47,XX, +8/46,XX.’ Clinical Genetics, 7, 232-237. 228. ALVESALO, L., OSBORNE, R. A., KARI, M. (1975) ‘The 47,XYY male, Y chromosome, and tooth size.’ American Journal of Human Genetics, 27, 53-61. 229. ARMENDARES, S. SALAMANCA, F. NAVA, S., NAVIREZ, S., CANTU, J.-M. (1975) ‘The 12p syndrome.’ Semaine des Hbpitaux. Annales de GPnPtique, 18, 89-94. 230. ATKINS, L., MILUNSKY, A., SHAHOOD, J. M. (1974) ‘Prenatal diagnosis: detailed chromosomal analysis in 500 cases.’ Clinical Genetics, 6, 3 17-322. 231. AURIAS, A., LAURENT, C. (1975) ‘Trisomy l lq . A new syndrome.’ (French.) Semaine des Hbpitaux. Annales de Gknktique, 18, 189-191. 232. AURIAS, A., TURC, C., MICHIELS, Y., SINET, P.-M., GRAVELEAU, D., LEJEUNE, J. (1975) ‘Two cases of trisomy 1 lq(q231 -+qter) due to translocation t(ll;22) (q23 1 ;ql11) in two different families.’ (French.) Semaine des Hbpitaux. Annales de GPndtique, 18,

[1]  J. Yunis,et al.  New chromosomal syndromes. , 1977, American journal of diseases of children.

[2]  R. Ablow,et al.  Trisomy 8 mosaicism syndrome. , 1975, Pediatrics.

[3]  L. Saxén,et al.  ASSOCIATION BETWEEN MATERNAL INTAKE OF DIAZEPAM AND ORAL CLEFTS , 1975, The Lancet.

[4]  E. Passarge,et al.  Alpha1-antitrypsin phenotypes in sex chromosome mosaicism. , 1975, Journal of medical genetics.

[5]  J. Cantú,et al.  Human acrocentric ring chromosomes and satellite association. , 1975, Annales de genetique.

[6]  J. Delhanty,et al.  Specific chromosome aberrations in ataxia telangiectasia. , 1975, Journal of medical genetics.

[7]  J. Boué,et al.  Identification of C trisomies in human abortuses. , 1975, Journal of medical genetics.

[8]  R. Coco,et al.  Partial 9 trisomy by 3:1 segregation of balanced maternal translocation (7q+; 9q-). , 1975, Journal of medical genetics.

[9]  P. L. Townes,et al.  Further identification of a D/E translocation. , 1975, American journal of diseases of children.

[10]  G. Dewald,et al.  A diploid‐triploid human mosaic with cytogenetic evidence of double fertilization , 1975, Clinical genetics.

[11]  L. Barta,et al.  Simultaneous occurrence of diabetes, liver cirrhosis, and 47, XX,21 +/46, XX chromosomal pattern. , 1975, Archives of disease in childhood.

[12]  S. Duck,et al.  Pseudohermaphroditis, with testes and a 46, XX karyotype. , 1975, The Journal of pediatrics.

[13]  F. A. Valentine,et al.  Segregation of a t(14q22q) chromosome in a large kindred , 1975, Clinical genetics.

[14]  A. T. Chen,et al.  CHROMOSOME STUDIES IN PREMATURE LOW BIRTH WEIGHT INFANTS , 1975, Acta paediatrica Scandinavica.

[15]  D. Rimoin,et al.  Human X-autosome translocations: differential inactivation of the X chromosome in a kindred with an X-9 translocation. , 1975, American journal of human genetics.

[16]  A. Rosenmann,et al.  Dicentric X‐isochromosome (Xqi dic) and pericentric inversion of No. 2 inv(2) (p15) q21) in a patient with gonadal dysgenesis , 1975, Clinical genetics.

[17]  E. Engel,et al.  A G-like trisomy with a major 15 proximal supernumerary component derived from a D/E balanced maternal interchange. , 1975, The Journal of pediatrics.

[18]  K. Halmi,et al.  Familial trisomy 7 mosaicism. , 1975, Journal of medical genetics.

[19]  V. Penchaszadeh,et al.  A case of ring 18 chromosome in a sibship with multiple spontaneous abortions. , 1975, Annales de genetique.

[20]  V. Penchaszadeh,et al.  Trisomy 22. Two new cases and delineation of the phenotype. , 1975, Journal of medical genetics.

[21]  M. Stefanini,et al.  A family with three sibs carrying trisomy 21. , 1975, Annales de genetique.

[22]  P.,et al.  Dermatoglyphic findings in 54 triple-X females and a review of some general principles applying to the soles in sex chromosome aneuploidy. , 1975, Journal of medical genetics.

[23]  J. Philip.  GONADOBLASTOMA IN DYSGENETIC GONADS WITH A Y CHROMOSOME , 1975, The Lancet.

[24]  R. Cleary,et al.  Prenatal sex detection with endocervical smears: successful results utilizing Y-bodyfluoroscence. , 1975, American journal of obstetrics and gynecology.

[25]  G. Hennigar,et al.  Mosaic double aneuploidy of X and G chromosomes. , 1975, American journal of mental deficiency.

[26]  L. Linarelli,et al.  Anomalies associated with partial deletion of long arm of chromosome 11. , 1975, The Journal of pediatrics.

[27]  Y. Kuroki,et al.  Two cases of 8p trisomy in one sibship , 1975, Clinical genetics.

[28]  S. Yanagisawa,et al.  Symptoms of Turner's syndrome and interstitial heterochromatin in i(Xq) , 1975, Clinical genetics.

[29]  R. Haslam,et al.  Trisomy‐18 Mosaicism with Features of Russell‐Silver Syndrome , 1975, Developmental medicine and child neurology.

[30]  P. Benson.  GENE DOSAGE EFFECT IN TRISOMY 21 , 1975, The Lancet.

[31]  K. Fried,et al.  Mental retardation and congenital malformations associated with a ring chromosome 6 , 1975, Clinical genetics.

[32]  M. Nelson,et al.  CHROMOSOMES IN ATAXIA-TELANGIECTASIA , 1975, The Lancet.

[33]  B. Migeon,et al.  Evidence for the inactivation of an X chromosome early in the development of the human female. , 1975, American journal of human genetics.

[34]  K. Fried,et al.  Ring chromosome 13 syndrome , 1975, Clinical genetics.

[35]  W. Centerwall,et al.  Translocation 4p-- syndrome: a general review. , 1975, American journal of diseases of children.

[36]  R. Neu,et al.  4p- phenotype in an infant with t(4p-;19p or q+)mat translocation. , 1975, American journal of diseases of children.

[37]  B. Korf,et al.  SEX-CHROMOSOME ABNORMALITIES IN HUSBANDS AND WIVES , 1975, The Lancet.

[38]  G. Stalder,et al.  POSSIBLE MOSAIC XXX-XXY MARRIAGE WITH ABNORMAL OFFSPRING , 1975, The Lancet.

[39]  J. G. Brewen,et al.  Analysis of X-ray-induced chromosomal translocations in human and marmoset spermatogonial stem cells , 1975, Nature.

[40]  R. Donald,et al.  Isochromosome for the short arm of X: A human mosaic 45,X/46,XXpi , 1975, Clinical genetics.

[41]  E. Kohne,et al.  [Neonatal polycythaemia and haemoglobin types in infants with G-trisomy (author's transl)]. , 1975, Klinische Wochenschrift.

[42]  H. Verhaaren,et al.  A new case of the trisomy 9p syndrome: Report of a patient with unusual chromosome findings (46,XX/47,XX, + i (9p)) and a peculiar congenital heart defect , 1975, Clinical genetics.

[43]  J. Bauman,et al.  An XX male: Cytogenetic and endocrine studies , 1975, Clinical genetics.

[44]  J. Kunze,et al.  A1 AND C9 MARKER CHROMOSOMES IN CHILDREN WITH COMBINED MINOR AND MAJOR MALFORMATIONS , 1975, The Lancet.

[45]  R. G. Davidson,et al.  A familial F/G translocation [t(20p‐; 22q+)] observed in three generations , 1975, Clinical genetics.

[46]  M. Mattei,et al.  [Trisomy 8 in mosaicism]. , 1975, Archives francaises de pediatrie.

[47]  S. Povey,et al.  Chromosome assignment of some human enzyme loci: mitochondrial malate dehydrogenase to 7, mannosephosphate isomerase and pyruvate kinase to 15 and probably, esterase D to 13 , 1975, Annals of human genetics.

[48]  J. Parrington,et al.  Elucidation of a pericentric inversion of a D‐group chromosome in the mother of a child with Patau's syndrome , 1975, Annals of human genetics.

[49]  M. Kekomäki,et al.  OXIDATION OF GLUCOSE and D‐B‐OH‐BUTYRATE BY THE EARLY HUMAN FETAL BRAIN , 1975, Acta paediatrica Scandinavica.

[50]  C. Hux,et al.  Incidence of tetraploidy as related to amniotic fluid cell types. , 1974, American journal of obstetrics and gynecology.

[51]  A. Vianna-Morgante,et al.  Turner's syndrome and 46,X,i(Yq) karyotype , 1974, Journal of medical genetics.

[52]  B. Crandall,et al.  The trisomy 8 syndrome: two additional mosaic cases , 1974, Journal of medical genetics.

[53]  M. Mikkelsen,et al.  Karyotype 45,XX,−21/46,XX,21q− in an infant with symptoms of G-deletion syndrome I , 1974, Journal of medical genetics.

[54]  M. Steele,et al.  Trisomy for the distal half of the long arm of chromosome no. 18. A report of two affected sibs. , 1974, The Journal of pediatrics.

[55]  K. Hirschhorn,et al.  Trisomy 21 mosaicism in a woman with two children with trisomy 21 Down's syndrome , 1974, Journal of medical genetics.

[56]  G. F. Smith,et al.  Chromosomal abnormality associated with congenital macroglossia and other abnormalities. , 1974, Journal of medical genetics.

[57]  R. Gordon,et al.  A case of partial trisomy 15 , 1974, Journal of medical genetics.

[58]  L. Zergollern.  Three generations and seven family members with a t(21q22q) chromosome. , 1974, Journal of medical genetics.

[59]  K. Laurence,et al.  Prenatal detection of D trisomy , 1974, Journal of medical genetics.

[60]  R. Rustad,et al.  Prenatal evaluation in a case of familial Y chromosome long arm deletion (Yq—) , 1974, Journal of medical genetics.

[61]  J. Cravioto,et al.  IONISING RADIATION AND CHROMOSOMAL ABERRATIONS IN MALNUTRITION , 1974 .

[62]  F A Baughman,et al.  The carrying angle in sex chromosome anomalies. , 1974, JAMA.

[63]  P. Masters,et al.  A familial 10/13 translocation: partial trisomy C in an infant associated with familial 10/13 translocation , 1974, Clinical genetics.

[64]  B. Crandall,et al.  Dominant piebald trait in a retarded child with a reciprocal translocation and small intercalary deletion. , 1974, American journal of human genetics.

[65]  J. Money,et al.  Cytogenetics, hormones and behavior disability: comparison of XYY and XXY syndromes , 1974, Clinical genetics.

[66]  A. Chapelle,et al.  Pericentric inversions of human chromosomes 9 and 10. , 1974, American journal of human genetics.

[67]  T. Thelen,et al.  A familial X-22 translocation with an extra X chromosome. , 1974, American journal of human genetics.

[68]  A. Connon.  ANTENATAL DIAGNOSIS OF SPINA BIFIDA , 1974, The Journal of obstetrics and gynaecology of the British Commonwealth.

[69]  M. Faed,et al.  47, XYY chromosome constitution, physical growth and psychological disturbance. A case study. , 1974, Journal of child psychology and psychiatry, and allied disciplines.

[70]  G. Sutherland,et al.  Chromosome studies in investigation of stillbirths and neonatal deaths* , 1974, Archives of disease in childhood.

[71]  A. Tanae,et al.  An XYY baby with Prader syndrome , 1974, Clinical genetics.

[72]  A. Klopper,et al.  A patient with a dicentric Y chromosome , 1974, Clinical genetics.

[73]  A. Ebbin,et al.  Inherited partial duplication of chromosome No. 15 , 1974, Journal of medical genetics.

[74]  B. Korf,et al.  A 21/21 tandem translocation with satellites on both long and short arms , 1974, Journal of medical genetics.

[75]  K. Fried,et al.  Familial translocation 15/22. A possible cause for abortions in female carriers , 1974, Journal of medical genetics.

[76]  H. Dosik,et al.  48,XXX, +18 double trisomy , 1974 .

[77]  P. Justice,et al.  An unusual chromosomal segregation in a family with a translocation between chromosomes 3 and 12 , 1974, Journal of medical genetics.

[78]  H. Rott,et al.  Partial trisomy 9 in the case of familial translocation 8/9 mat. , 1974, Annales de genetique.

[79]  C. Blank,et al.  Multiple congenital defects associated with trisomy for the short arm of chromosome 4 , 1974, Journal of medical genetics.

[80]  Á. Hreidarsson,et al.  Frequency of deletion of short arm satellites in acrocentric chromosomes , 1974, Journal of medical genetics.

[81]  J. Hamerton,et al.  A 48,XXXX female , 1974, Journal of medical genetics.

[82]  U. Francke,et al.  Translocation, t(4q−;13q+), in three generations resulting in partial trisomy of the long arm of chromosome 4 in the fourth generation , 1974 .

[83]  K. Laurence,et al.  Deletion of the long arms of the Y chromosome with normal male development and intelligence , 1974, Journal of medical genetics.

[84]  W. Vogel,et al.  Partial trisomy 7q. , 1973, Annales de genetique.

[85]  J. Van Biervliet,et al.  Familial occurrence of the g syndrome. , 1975, Clinical genetics.

[86]  T. David,et al.  Dermatoglyphic diagnosis of the poland anomaly in the absence of syndactyly. , 1974, Human heredity.

[87]  F. Ruddle,et al.  Assignment of a gene for adenosine deaminase to human chromosome 20. , 1974, Human heredity.

[88]  W. Schmid.  The prenatal diagnosis of chromosome anomalies. , 1972, Triangle; the Sandoz journal of medical science.

[89]  R. Summitt.  DELETION OF THE SHORT ARM OF CHROMOSOME 18. , 1964, Cytogenetics.

[90]  H. Rott,et al.  Pseudohermaphroditism with clinical features of trisomy 18 in an infant trisomic for parts of chromosomes 16 and 18 , 2022 .

[91]  LillianY. F. Hsu,et al.  tri-Partial 12p deletion: a cause for a mental retardation, multiple congenital abnormality syndrome , 2022 .

[92]  C. V. K. H. '. M. Roepaan.  A patient with congenital anomalies and a deletion of the long arm of chromosome 4 , 2022 .