Human Genetics - 1973

108 articles | Last updated: 2025-12-03 14:12:56

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Article Title	Cauc.		White		Euro.		Other		Phrases Used
Article Title	T	A	T	A	T	A	T	A	Phrases Used
Multiple anomalies associated with an extra small metacentric chromosome: Modified Giemsa stain results
Trisomie 10 partielle par translocation familiale t(1;10) (q44;q22)
Zwei subterminale Heterochromatinregionen bei einer seltenen Form einer 21/21-Translokation
Zur Beziehung zwischen Hautleistenverlauf und Morbus Wilson
Die Bestimmung der sauren Erythrocytenphosphatase(SEP)-Isoenzyme mit der Celluloseacetatfolien-Elektrophorese
Untersuchungen zum GPT-System unter besonderer Ber�cksichtigung des stummen Allels GPT0
Variation in the nonfluorescent segment of long Y chromosome
Spatial relations of human chromosomes identified by quinacrine fluorescence at metaphase
Spatial relations of human chromosomes identified by quinacrine fluorescence at metaphase
A child with a 21-ring chromosome, 45,XX,21-/46,XX,21r investigated with the banding technique
A chromosome study in multiple sclerosis
Daten zur Populationsgenetik der Adenosin-Desaminase (E.C. 3.5.4.4) aus Schleswig-Holstein
Metaphase chromosomes from neonatal urine
The development of the antigenic structures of human ?1-antichymotrypsin and C 1 q
Spontaneous chromosomal instability
Zur Unterscheidung zwischen multifaktoriellem Erbgang mit Schwellenwerteffekt und einfachem diallelen Erbgang
Synopsis of mammo-renal syndromes. II
Age determination by immunological techniques of the last common ancestor of man and chimpanzee
Inherited translocations in two families (t(14q+;10q?) and t(13q?;21q+))
Changes of the synaptonemal complex at the end of pachytene
Is the PGM1 locus subject to selection?
Lactate dehydrogenase isoenzymes in the mammalian egg: Investigations by micro disc electrophoresis in 15 species of the orders Rodentia, Lagomorpha, Carnivora, Artiodactyla and in man
Combined klinefelter-Down syndrome or XXYY syndrome?
Pericentric Y inversion in the general population
Father and daughter with presumptive isochromosome satellites-short arms D or G
Chromsomal analysis of two consecutive abortuses in each of 43 women
Structural aberration in chromosome No. 2
Study of LDH variants amongst the Mundas in Ranchi district, Bihar, India
An attempt to establish trisomy 8 syndrome
Studium der schwachen B-Variante in einer Familie
Possible mechanisms of human teratogenesis by imperfect potato
Lipid-peroxidation in Spielmeyer-Vogt's disease
Giemsa ?banding? in metaphase chromosomes after pretreatment with inactivated trypsin
Genetic polymorphism of mannosephosphate isomerase in Primates
Genetic polymorphism of Isocitrate dehydrogenase in Primates
Transspecific variability of carbonic anhydrase I in Primates
Genetic polymorphism of liver esterases in Primates
X0 Karyotype in a phenotypic male
Humeroradial synostosis
A 4p- syndrome
Genetisch determinierter polymorphismus der menschlichen serum-paraoxonase (EC 3.1.1.2)
Schlu�wort
Inheritance of the enzyme deficiency in three neurolipidoses: variant 0 of Tay-Sachs disease (Sandhoff's disease), classic tay-sachs disease, and metachromatic leukodystrophy. Identification of the he
Haptoglobin types and subtypes in Alzheimer's disease and senile dementia
Wahrscheinliche genetische Belastung der Bev�lkerung mit ?INH? (Isonicotins�ure-Hydrazid)
On the distinction between chromosomes No. 21 and No. 22 by the C-banding pattern
A microculture method for chromosome preparations from total human and rabbit blood
Late DNA replication pattern of human chromosomes determined by means of 3H-Deoxycytidine
Parental age in retinoblastoma
Syndrome de Rubinstein-Taybi
A t(13q14q) family with the translocation and a Philadelphia chromosome in one member
Elektronenmikroskopische Untersuchung interchromosomaler f�diger Strukturen an menschlichen Lymphocyten in der Metaphase
Two rare GPT phenotypes in a Norwegian family
De novo translocation t(Yq?; 15p+) in a malformed boy
Determination of the threshold value of the mutagenic activity of Trenimon� on human lymphocytes ?in vitro?
A mother-child combination analysis for AB0-Hp interaction
Polymorphismus des konstitutiven Heterochromatins bei menschlichen A1-Metaphasechromosomen
Chromosome number 18
Partielle Trisomie des kurzen Arms eines Chromosoms Nr. 4 in der Folge einer Translokation t(4p-22p+)
Partial trisomy 1, karyotype 46,XY,12-,t(1q, 12p)+
Chromosomes in patients treated with Azathioprine
Untersuchungen �ber die Beeinflussung der chromosomensch�digenden Aktivit�t von Trenimon� an menschlichen Lymphocyten in vitro durch Aminos�uren
Centromere staining at meiosis in man
Ph�notypes de la glucose-6-phosphate d�shydrog�nase �rythrocytaire dans la race noire							✓		race noire
Giemsa banding of a human metacentric chromosome number 9
A familial syndrome of unusual facies associated with malocclusion and short stature
�ber das einmalige Vorkommen eines klassischen Bogenmusters auf der Palma des Menschen
(6;15) Translocation with loss of chromosome material in the patient and various chromosome aberrations in family members
Identification of a familial 19/21 translocation by Q and G band patterns
C3 types and their inheritance in Finnish Lapps, Maris (Cheremisses) and Greenland Eskimos
The Sj�gren-Larsson syndrome
Polymorphism of C'3 in German, Bulgarian, Iranian and Angola population							✓		German, Bulgarian, Iranian and Angola population
Phenotype and gene frequencies of adenosine deaminase in prague
Hereditary methemoglobinemia associated with NADH diaphorase deficiency
Sex ratio among human embryos and newborns in a Russian population
Chromosomenmosaik 46,XY,D-,t(DqGq)+/92,XYXY,2D-,2t(DqGq)+ bei einem S�ugling mit Down-Syndrom
�ber die ultrastruktur menschlicher Metaphasenchromosomen
A casuistic contribution to the XX male problem
Identification of D/D translocations in mentally retarded patients
The occurrence of G-6-PD union in Thailand
Tetraphocomelia and neonatal amegakaryocytic thrombocytopenia
Malformations of kidney and urinary tract in common chromosomal aberrations
Parental mean ages and birth order in different types of congenital heart defects
Characterization of glucose-6-phosphate dehydrogenase in Thailand
Acute myeloid leukemia with two philadelphia chromosomes in forty-six stemline
Ribosomal cistrons and acrocentric chromosomes in man
Banding patterns of the chromosomes of man and the chimpanzee
Heated giemsa solution for producing more consistent bands on mammalian chromosomes
On the genetics of the primary generalized epilepsy with sporadic myoclonias of impulsive petit mal type
Further studies on associations between leprosy and genetic markers in human serum
Abnormal (marker) chromosomes in a quinacrine-treated patient with isospora belli and Giardia lamblia
Identification of a familial robertsonian translocation t(13q14q) by means of thermic moderated denaturation
The influence of inactive chromosomes on human development
Malformations of kidney and urinary tract in common chromosomal aberrations
Distribution of constitutive heterochromatin in Hela and HEp-2 cell lines
A comparison between quinacrine fluorescence banding and 3H-thymidine incorporation patterns in human chromosomes
Occurrence of XYY individuals among juvenile delinquents in Hungary
Autosomal dominant inheritance in adiposis dolorosa (Dercum's disease)
Red-cell galactose-1-phosphate-uridyl transferase (EC: 2.7.7.12)
Serum dependency of cellular phenotype in mucopolysaccharidoses: The influence of autologous serum on metachromasia
Autosomal rings and variable phenotypes
Fluorescence banding pattern of the chromosomes of Microtus agrestis with a benzimidazol derivative
Banding patterns and late replication in HeLa cells
Unterschiede zwischen Mutter-kind- und Vater-Kind-Korrelationen im Hautleistensystem des Menschen
Dominant lethal test in the mouse for mutagenic effects of saccharine
Polymorphismus der menschlichen Erythrocyten-Glutamat-Pyruvat-Transminase
Iminoglycinuria in a child in Czechoslovakia
Zwei subterminale Heterochromatinregionen bei einer seltenen form einer 21/21-translokation