Primary hypothyroidism, growth hormone deficiency and congenital malformations in a child with the karyotype 46,XY,del(1)(q25q32).

scientific article published in July 1976

Primary hypothyroidism, growth hormone deficiency and congenital malformations in a child with the karyotype 46,XY,del(1)(q25q32). is …
instance of (P31):
scholarly articleQ13442814

External links are
P356DOI10.1111/J.1651-2227.1976.TB04923.X
P698PubMed publication ID937003

P2093author name stringAkerblom HK
Koivisto M
de La Chapelle A
Remes M
P2860cites workUse of activated charcoal in the radioimmunoassay of human growth hormone in plasmaQ36551184
RING-1 CHROMOSOME AND MICROCEPHALIC DWARFISMQ41939552
P433issue4
P921main subjectkaryotypeQ189967
growth hormone deficiencyQ369262
P304page(s)513-518
P577publication date1976-07-01
P1433published inActa Paediatrica ScandinavicaQ27708772
P1476titlePrimary hypothyroidism, growth hormone deficiency and congenital malformations in a child with the karyotype 46,XY,del(1)(q25q32).
P478volume65

Reverse relations

cites work (P2860)
Q34468912A patient defines the interstitial 1q deletion syndrome characterized by antithrombin III deficiency.
Q34997016Current approaches for deciphering the molecular basis of combined anterior pituitary hormone deficiency in humans
Q68586990Cytogenetic analysis in congenital hypothyroidism
Q41934201De novo deletion of 1q31.1-q32.1 in a patient with developmental delay and behavioral disorders
Q33584670De novo interstitial deletion del(1)(p21p32)
Q72108918Immune function in patients with chromosome deletions
Q51945810Interstitial 1q25.3‐q31.3 deletion in a boy with mild manifestations
Q41847533Interstitial deletion in the long arms of chromosome 1: 46,XY,del(1)(pter leads to q22::q25 leads to qter).
Q41932489Interstitial deletion of chromosome 1 [del(1)(q25q32)] in an infant with prune belly sequence
Q35202320Partial trisomy 1 due to a "shift" and probable location of the Duffy (Fy) locus
Q41936487Terminal deletion of the long arm of chromosome 1 in a malformed newborn
Q41684207Terminal long-arm deletion of chromosome 1 in a male infant

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